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2026-09-03 14:11 6d ago
2026-09-03 07:45 6d ago
Emergent BioSolutions provedla zpětný odkup dluhu za 75 milionů USD
EBS Emergent Biosolutions
FMP Stock News 78
Original source text
 | Source: Emergent BioSolutions

Repurchase reduces unsecured note balance to approximately $364.7 millionManagement to discuss this key milestone and broader transformation progress at upcoming investor conferences GAITHERSBURG, Md., Sept. 03, 2026 (GLOBE NEWSWIRE) -- Emergent BioSolutions Inc. (NYSE: EBS) today announced that it has completed the repurchase of $75 million aggregate principal amount of its 3.875% Senior Unsecured Notes due 2028 (the “Senior Unsecured Notes”), following authorization granted by its Board of Directors. In total, Emergent deployed approximately $68 million of cash for the repurchases, resulting in an average repurchase price of 90.6% of face value. Following completion of the repurchases, the outstanding aggregate principal balance of the Senior Unsecured Notes has been reduced to approximately $364.7 million.

“This bond repurchase reflects our continued discipline in deploying capital to strengthen Emergent’s financial profile while maintaining flexibility to support our strategic growth priorities,” said Joe Papa, president and CEO of Emergent. “The transactions were executed at attractive market levels, reduced our outstanding unsecured debt and further demonstrate our commitment to prudent balance sheet management as we continue advancing our multi-year transformation plan.”

Emergent continues to maintain a strong cash position on its balance sheet and has access to an additional $50 million under its asset-based revolving loan facility, providing liquidity to support the company’s ongoing key strategic priorities. The company also plans to continue to monitor market conditions and evaluate the optimal timing for refinancing the remaining outstanding Senior Unsecured Notes, which mature in August 2028.

Emergent management will discuss this important milestone, along with the company’s broader transformation progress, at the following investor conferences:

21st Annual Wells Fargo Healthcare Conference, September 9, 2026H.C. Wainwright 28th Annual Global Investment Conference, September 14, 2026Presentation and webcast to be held at 3:30 pm ET; register here. A replay will be made available on Emergent’s Investor page. About Emergent BioSolutions 
At Emergent, our mission is to protect and save lives. For over 25 years, we’ve been at work preparing those entrusted with protecting public health. We deliver protective and life-saving solutions for health threats like smallpox, mpox, botulism, Ebola, anthrax and opioid overdose emergencies. To learn more about how we help prepare communities around the world for today’s health challenges and tomorrow’s threats, visit our website and follow us on LinkedIn, X, Instagram, Apple Podcasts and Spotify. 

Safe Harbor Statement
This press release includes forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. All statements, other than statements of historical fact, including statements regarding our ability to opportunistically deploy capital, the potential refinancing of additional Senior Unsecured Notes and our multi-year transformation plan, are forward-looking statements. We generally identify forward-looking statements by using words like "anticipate," "believe," "continue," "could," "estimate," "expect," "forecast," "future," "goal," "intend," "may," "plan," "position," "possible," "potential," "predict," "project," "should," "target," "will," "would," and similar expressions or variations thereof, or the negative thereof, but these terms are not the exclusive means of identifying such statements.

These forward-looking statements are based on our current intentions, beliefs and expectations regarding future events based on information that is currently available. We cannot guarantee that any forward-looking statement will be accurate. Readers should realize that if underlying assumptions prove inaccurate or unknown risks or uncertainties materialize, actual results could differ materially from our expectations. Readers are, therefore, cautioned not to place undue reliance on any forward-looking statement, as contained herein. Any such forward-looking statement speaks only as of the date of this press release, and, except as required by law, we do not undertake any obligation to update any forward-looking statement to reflect new information, events or circumstances.

There are a number of important factors that could cause the company's actual results to differ materially from those indicated by any forward-looking statements. Readers should consider this cautionary statement, as well as the risks identified in our periodic reports filed with the U.S. Securities and Exchange Commission, when evaluating our forward-looking statements.

Investor Contact:
Richard S. Lindahl
Executive Vice President, CFO
[email protected]

Media Contact:
Assal Hellmer
Vice President, Communications
[email protected]
2026-09-01 13:24 8d ago
2026-09-01 07:55 8d ago
Emergent BioSolutions získala kontrakt na vakcínu CYFENDUS
EBS Emergent Biosolutions
FMP Stock News 86
Original source text
GAITHERSBURG, Md., Sept. 01, 2026 (GLOBE NEWSWIRE) -- Emergent BioSolutions Inc. (NYSE: EBS) today announced a contract modification valued at approximately $24 million from the Biomedical Advanced Research and Development Authority (BARDA), part of the Administration for Strategic Preparedness and Response (ASPR) within the U.S. Department of Health and Human Services (HHS), to supply CYFENDUS® (Anthrax Vaccine Adsorbed, Adjuvanted) for anthrax preparedness efforts. Anthrax remains a significant global biological threat due to its potential use in a bioterrorism event and its implications for public health and national security.

“This newly executed CYFENDUS® contract modification with the U.S. government highlights the continued importance of maintaining readiness against anthrax threats,” said Paul Williams, senior vice president, head of products business, global government & public affairs at Emergent. “Emergent remains committed to ensuring access to CYFENDUS® and strengthening preparedness through reliable domestic manufacturing and supply.”

CYFENDUS® was approved by the U.S. Food and Drug Administration in July 2023 as a two-dose anthrax vaccine for post-exposure prophylaxis use in individuals 18 through 65 years of age when given with recommended antibacterial drugs. A recent NEJM Evidence study by Tillman et al. examines the use of the CYFENDUS® vaccine for post-exposure prophylaxis following anthrax exposures in Wyoming, further reinforcing the importance of maintaining preparedness capabilities and access to effective medical countermeasures against this high-consequence biological threat.1

This award builds on Emergent’s work with the U.S. government to support anthrax preparedness. Earlier this year, Emergent announced a delivery order valued at up to $21.5 million to supply BioThrax® (Anthrax Vaccine Adsorbed) to the U.S. Department of War.

This project has been funded in whole or in part with federal funds from the U.S. Department of Health and Human Services, Administration for Strategic Preparedness and Response, Biomedical Advanced Research and Development Authority, under Contract No. HHSO100201600030C.

About CYFENDUS® (Anthrax Vaccine Adsorbed, Adjuvanted)

Indication

CYFENDUS® (Anthrax Vaccine Absorbed, Adjuvanted) is a vaccine indicated for post-exposure prophylaxis of anthrax disease following suspected or confirmed exposure to Bacillus anthracis in persons 18 through 65 years of age when given with recommended antibacterial drugs. The efficacy of CYFENDUS® vaccine for post-exposure prophylaxis (PEP) is based solely on studies in animal models of inhalational anthrax.

Important Safety Information

Contraindication: Do not administer CYFENDUS® to individuals with a history of a severe allergic reaction (e.g., anaphylaxis) following a previous dose of CYFENDUS®, BioThrax® (a licensed anthrax vaccine with the same active ingredient as CYFENDUS®) or any component of the vaccine.

Warnings and Precautions: Management of Acute Allergic Reactions: Appropriate medical treatment must be available to manage possible anaphylactic reactions following administration of CYFENDUS®. Pregnancy: CYFENDUS® can cause fetal harm when administered to a pregnant individual. In an observational study, there were more birth defects in infants born to individuals vaccinated with BioThrax® (a licensed anthrax vaccine with the same active ingredient as CYFENDUS®) in the first trimester compared to infants born to individuals vaccinated post pregnancy or individuals never vaccinated with BioThrax®.

Adverse Reactions: The most common (≥10%) injection-site adverse reactions reported were tenderness, pain, arm motion limitation, warmth, induration, itching, swelling, and erythema/redness. The most common systemic adverse reactions were muscle aches, tiredness, and headache.

To report Suspected Adverse Reactions, contact Emergent BioSolutions at 1-800-768-2304 or [email protected]; or VAERS at 1-800-822-7967 or www.vaers.hhs.gov.

Please see the Prescribing Information for CYFENDUS® for full safety information.

About BioThrax® (Anthrax Vaccine Adsorbed) 
BioThrax® vaccine is indicated for the active immunization for the prevention of disease caused by Bacillus anthracis in persons 18 through 65 years of age. BioThrax® is approved for (1) pre-exposure prophylaxis of disease in persons at high risk of exposure; and (2) post-exposure prophylaxis of disease following suspected or confirmed Bacillus anthracis exposure, when administered in conjunction with recommended antibacterial drugs. The efficacy of BioThrax® for post-exposure prophylaxis is based solely on studies in animal models of inhalational anthrax. 

Select Important Safety Information 

Contraindication: Severe allergic reaction (e.g., anaphylaxis) after a previous dose of BioThrax® or a component of the vaccine. Warnings and Precautions: Latex: The stopper of the vial contains natural rubber latex and may cause allergic reactions in latex sensitive individuals. Pregnancy: Avoid use in pregnancy unless the potential benefit outweighs the potential risk to the fetus. Adverse Reactions: The most common (>10%) local (injection-site) adverse reactions observed in clinical studies were tenderness, pain, erythema, edema, and arm motion limitation. The most common (≥5%) systemic adverse reactions were muscle aches, fatigue, and headache. 

Please see the full Prescribing Information for BioThrax® for additional safety information. 

About Emergent BioSolutions 
At Emergent, our mission is to protect and save lives. For over 25 years, we’ve been at work preparing those entrusted with protecting public health. We deliver protective and life-saving solutions for health threats like smallpox, mpox, botulism, Ebola, anthrax and opioid overdose emergencies. To learn more about how we help prepare communities around the world for today’s health challenges and tomorrow’s threats, visit our website and follow us on LinkedIn, X, Instagram, Apple Podcasts and Spotify. 

Safe Harbor Statement
This press release includes forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. All statements, other than statements of historical fact, including statements regarding the expected timing for delivery of the CYFENDUS® vaccine and Emergent’s ability to increase inventories of CYFENDUS® vaccine to meet requested levels within specified time frames, are forward-looking statements. We generally identify forward-looking statements by using words like “anticipate,” “believe,” “continue,” “could,” “estimate,” “expect,” “forecast,” “goal,” “intend,” “may,” “plan,” “should,” “will,” “would,” and similar expressions or variations thereof, or the negative thereof, but these terms are not the exclusive means of identifying such statements. Forward-looking statements are based on our current intentions, beliefs, and expectations regarding future events based on information that is currently available. We cannot guarantee that any forward-looking statement will be accurate. Readers should realize that if underlying assumptions prove inaccurate or if known or unknown risks or uncertainties materialize, actual results could differ materially from our expectations. Readers are, therefore, cautioned not to place undue reliance on any forward-looking statement. Any forward-looking statement speaks only as of the date of this press release, and, except as required by law, we do not undertake to update any forward-looking statement to reflect new information, events, or circumstances. Readers should consider this cautionary statement, as well as the risk factors identified in our periodic reports filed with the U.S. Securities and Exchange Commission, when evaluating our forward-looking statements.

Investor Contact:
Richard S. Lindahl
Executive Vice President, CFO
[email protected]

Media Contact:
Assal Hellmer
Vice President, Communications
[email protected]

1Tillman, C., Waranius, B. N., Van Houten, C., & Harrist, A. (2026). Cyfendus for Postexposure Prophylaxis after Inhalation Anthrax Exposures in Wyoming. NEJM Evidence, 5(7), EVIDpha2600122. doi.org.
2026-08-31 13:06 9d ago
2026-08-31 07:55 9d ago
Kanada zadala Emergent BioSolutions zakázku na dodávky NARCAN
EBS Emergent Biosolutions
FMP Stock News 86
Original source text
Standing offer expands access to opioid overdose emergency treatment across participating federal, provincial and territorial organizations in Canada WINNIPEG, Manitoba, Aug. 31, 2026 (GLOBE NEWSWIRE) -- Emergent BioSolutions Inc. (NYSE: EBS) today announced that it has been awarded a standing offer by the Government of Canada, through a competitive procurement process, to supply NARCAN® Nasal Spray. The standing offer is effective from October 1, 2026, through September 30, 2029, with an option to extend for an additional two years.

Under the standing offer, authorized federal departments, agencies, Crown corporations, provinces, territories and other designated public sector organizations across Canada may procure NARCAN® Nasal Spray through individual call-ups, helping support timely access to overdose reversal medication in communities nationwide.

"Canada continues to face a significant public health challenge from the opioid crisis and expanding access to naloxone remains a critical component of overdose response efforts," said Paul Williams, head of products business, global government & public affairs at Emergent. "We are proud that the Government of Canada has selected NARCAN® Nasal Spray under this standing offer, reinforcing our commitment to helping to protect and save lives."

NARCAN® Nasal Spray is designed to reverse the effects of an opioid poisoning in minutes and is the only 4 mg, intranasal naloxone spray in Canada with a shelf life of four years (48 months). This award follows an existing 5-year standing offer between Emergent and the Government of Canada set to expire in September 2026.

"As communities across Canada continue efforts to prevent opioid poisoning deaths, we remain focused on ensuring broad availability of NARCAN® Nasal Spray and supporting public health preparedness," added Danielle Portnik, vice president and general manager at Emergent. "We appreciate the opportunity to continue working with the Government of Canada to improve access to this lifesaving treatment."

About NARCAN® Nasal Spray

NARCAN® Nasal Spray is a pure opioid antagonist indicated for emergency use to reverse known or suspected opioid overdose, as manifested by respiratory and/or severe central nervous system depression.

While NARCAN® Nasal Spray can be administered by a non-health care professional, it is not intended to be a substitute for professional medical care. Always call 911 as soon as an opioid overdose is suspected, before administering NARCAN® Nasal Spray.

Always read the label and follow the directions for use.

About Emergent BioSolutions 
At Emergent, our mission is to protect and save lives. For over 25 years, we’ve been at work preparing those entrusted with protecting public health. We deliver protective and life-saving solutions for health threats like smallpox, mpox, botulism, Ebola, anthrax and opioid overdose emergencies. To learn more about how we help prepare communities around the world for today’s health challenges and tomorrow’s threats, visit our website and follow us on LinkedIn, X, Instagram, Apple Podcasts and Spotify. 

Safe Harbor Statement
This press release includes forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. All statements, other than statements of historical fact, including statements regarding the availability and Canadian government procurement of NARCAN® Nasal Spray are forward-looking statements. We generally identify forward-looking statements by using words like “anticipate,” “believe,” “continue,” “could,” “estimate,” “expect,” “forecast,” “goal,” “intend,” “may,” “plan,” “should,” “will,” “would,” and similar expressions or variations thereof, or the negative thereof, but these terms are not the exclusive means of identifying such statements. Forward-looking statements are based on our current intentions, beliefs, and expectations regarding future events based on information that is currently available. We cannot guarantee that any forward-looking statement will be accurate. Readers should realize that if underlying assumptions prove inaccurate or if known or unknown risks or uncertainties materialize, actual results could differ materially from our expectations. Readers are, therefore, cautioned not to place undue reliance on any forward-looking statement. Any forward-looking statement speaks only as of the date of this press release, and, except as required by law, we do not undertake to update any forward-looking statement to reflect new information, events, or circumstances. Readers should consider this cautionary statement, as well as the risk factors identified in our periodic reports filed with the U.S. Securities and Exchange Commission, when evaluating our forward-looking statements.

Investor Contact:
Richard S. Lindahl
Executive Vice President, CFO
[email protected]

Media Contact:
Assal Hellmer
Vice President, Communications
[email protected]
2026-08-17 22:05 23d ago
2026-08-17 14:00 23d ago
Emergent BioSolutions zaúčtovala nepeněžní znehodnocení 191,3 milionu USD kvůli NARCAN
EBS Emergent Biosolutions
FMP Stock News 72
Original source text
Schall, Brown & Schwartz LLP (“SBS”), a national shareholder rights litigation firm, announces that it is investigating claims on behalf of investors of Emergent BioSolutions Inc. (“Emergent” or “the Company”) (NYSE: EBS) for violations of the securities laws.

INVESTIGATION DETAILS: The investigation focuses on whether the Company issued false and/or misleading statements and/or failed to disclose information pertinent to investors. Emergent revealed a $191.3 million non-cash impairment charge based on competition and pricing pressure on its NARCAN product line. Based on this news, shares of Emergent fell sharply.

If you are a shareholder who suffered a loss, click here to participate.

We also encourage you to contact Brian Schall or David Schwartz of Schall, Brown & Schwartz LLP, 2049 Century Park East, Suite 2460, Los Angeles, CA 90067, at 310-301-3335, to discuss your rights free of charge. You can also reach us through the firm's website at www.schallfirm.com, or by email at [email protected].

WHY SBS? Schall, Brown & Schwartz LLP represents investors around the world and specializes in securities class action lawsuits and shareholder rights litigation. Bringing together the extensive experience and diverse skillsets of founding partners Brian Schall, Andrew Brown, and David Schwartz, SBS is dedicated to aggressively advocating for every investor.

This press release may be considered Attorney Advertising in some jurisdictions under the applicable law and rules of ethics.

View source version on businesswire.com: https://www.businesswire.com/news/home/20260817756341/en/

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2026-08-08 06:54 1mo ago
2026-08-08 01:04 1mo ago
Emergent BioSolutions snížila výhled na celý rok kvůli tlaku na NARCAN
EBS Emergent Biosolutions
FMP Stock News 86
Original source text
3 Small-Cap Stocks to Watch After the Fed’s Rate CutsEmergent Biosolutions NYSE: EBS reported second-quarter 2026 revenue and adjusted EBITDA above its prior guidance and analyst consensus, driven by accelerated medical countermeasure deliveries to U.S. government customers. The company also lowered its full-year outlook as increased competition and pricing pressure in the naloxone market are expected to weigh on sales of NARCAN.

Revenue for the second quarter totaled $234 million, above the high end of the company’s prior guidance range of $185 million. Adjusted EBITDA was $97 million, representing a 41% margin, compared with $33 million and a 23% margin in the year-earlier period. Year-to-date revenue reached $390 million, up from $363 million in the first half of 2025, while adjusted EBITDA increased to $132 million from $112 million.

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Big Rallies Brewing? 3 Analyst Favorites to Watch CloselyChief Executive Officer Joseph Papa said the results reflected “strong execution and acceleration” of medical countermeasure, or MCM, deliveries during the quarter. MCM revenue totaled $168 million, which Papa said was the company’s highest second-quarter MCM revenue since 2020.

Medical Countermeasures Drive First-Half Performance Emergent said its MCM business remains a central growth driver, supported by contracts with the U.S. government and international customers. During the quarter, the company received a $52.7 million contract modification for ACAM2000 and a $64.5 million contract modification for botulism antitoxin. It secured more than 10 contract awards year to date.

Watch These 4 Overbought Stocks As Market Rotation ContinuesInternational MCM sales accounted for approximately 20% of total first-half 2026 MCM revenue, according to Papa. The company cited continued engagement with U.S. and allied governments amid heightened concerns about biodefense preparedness.

Papa also said Emergent is seeking to collaborate with artificial intelligence leaders and partners to address potential bioterrorism risks and improve preparedness. He noted that the company continues to pursue programs including TEMBEXA, Ebanga and Raxibacumab. The MOSA study in Africa, which is evaluating TEMBEXA in Mpox, has enrolled more than 100 patients, with additional sites being opened by the study sponsor and partners.

During the quarter, Emergent received Saudi Food and Drug Authority approval for ACAM2000 and approval from Singapore’s Health Sciences Authority to expand ACAM2000’s label to include an Mpox indication.

NARCAN Competition Prompts Restructuring and Impairment Management said the naloxone market changed late in the second quarter with a new 4-milligram over-the-counter nasal naloxone approval on June 16 and the anticipated August launch of a 10-milligram prescription product. The company also cited more aggressive pricing across the category.

Papa said Emergent believes NARCAN retains more than 50% of the naloxone market and remains the market leader. However, he said the company expects further price erosion as new competitors enter the market. Management expects overall naloxone unit demand to remain relatively flat.

In response, Emergent announced restructuring actions expected to generate about $40 million in annualized net savings. The measures include:

A reduction of approximately 90 positions; The closure of two wet laboratories in Maryland; The sale of an underutilized office building for $6.4 million; and An exit from a central warehouse lease. The company expects to incur approximately $11 million in costs to achieve the savings. Papa said the company will begin realizing some savings in 2026, with the full $40 million annualized run rate expected in 2027.

Chief Financial Officer Rich Lindahl said Emergent recorded a non-cash impairment charge of approximately $191 million during the second quarter related to the NARCAN asset group. The charge reflected the company’s revised assessment of expected future cash flows amid pricing and competitive developments. Lindahl said the impairment does not affect cash, liquidity, operating cash flow or adjusted EBITDA, but will reduce GAAP net income.

Emergent plans to seek growth in the commercial franchise through additional NARCAN offerings, including a carrying case, multipack configurations and wall kits.

Outlook Lowered on Commercial Revenue Pressure Emergent lowered its full-year 2026 revenue guidance to $645 million to $675 million, from a prior range of $720 million to $760 million. The revision primarily reflects lower expected commercial revenue in the second half due to increased NARCAN competition and naloxone pricing and volume pressure.

The company maintained its view that MCM revenue would be flat to slightly down for the full year, with the first-half benefit from accelerated deliveries already reflected in reported results.

GAAP net loss: $245 million to $225 million Adjusted net income: $10 million to $30 million Adjusted EBITDA: $130 million to $150 million, down from prior guidance of $155 million to $175 million Adjusted gross margin: 42% to 44% Third-quarter revenue: $110 million to $130 million At June 30, Emergent had $140 million in cash and $190 million in total liquidity. Gross debt was $590 million and net debt was $450 million. Lindahl said the company collected $145 million through July from accounts receivable outstanding at quarter-end, describing the collections as normal working-capital activity rather than a securitization or financing transaction.

The company completed a term loan refinancing in April, establishing a $150 million term loan maturing in 2031. Its board also authorized a $75 million program to repurchase senior unsecured notes. During the second quarter, Emergent repurchased 1.1 million shares for approximately $9 million, bringing year-to-date share repurchases to $18 million.

About Emergent Biosolutions (NYSE:EBS)Emergent BioSolutions is a global specialty biopharmaceutical company focused on developing, manufacturing and commercializing medical countermeasures and specialty products that address public health threats. The company's portfolio includes vaccines, antibody therapies and critical care products designed to protect against biological, chemical and emerging infectious disease threats. Emergent has longstanding partnerships with government agencies, including the U.S. Department of Defense and the Biomedical Advanced Research and Development Authority (BARDA), to support national preparedness programs.

Key commercial products in Emergent's lineup include BioThrax (anthrax vaccine adsorbed), ACAM2000 (smallpox vaccine) and Vaxchora (cholera vaccine), alongside therapeutic treatments such as Anthrasil (anthrax immune globulin) and the naloxone-based nasal spray Narcan for opioid overdose reversal.

This instant news alert was generated by narrative science technology and financial data from MarketBeat in order to provide readers with the fastest reporting and unbiased coverage. Please send any questions or comments about this story to [email protected].

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2026-08-05 21:09 1mo ago
2026-08-05 16:07 1mo ago
Emergent BioSolutions zvýšila tržby o 66 %, vykázala ztrátu
EBS Emergent Biosolutions
FMP Stock News 92
Original source text
Second Quarter 2026 Total Revenues of $234.3 million, an improvement of 66% versus prior yearSecond Quarter 2026 Net Loss of $180.2 million worsening 1,402% versus prior year, largely due to a $191.3 million non-cash impairment chargeSecond Quarter 2026 Adjusted Net Income of $30.9 million improved 134% versus prior yearSecond Quarter 2026 Gross Margin % of 50% and Adjusted Gross Margin % of 58%, an expansion of 1400 bps and 900 bps, respectively, versus prior yearSecond Quarter 2026 Adjusted EBITDA of $96.5 million and Adjusted EBITDA Margin of 41%, an improvement of 1,800 bps versus prior yearRestructuring business operations to align resourcing to current needs; expected to result in annualized savings of approximately $40 million when fully implemented GAITHERSBURG, Md., Aug. 05, 2026 (GLOBE NEWSWIRE) -- Emergent BioSolutions Inc. (NYSE: EBS) today reported financial results for the second quarter ended June 30, 2026.

“Emergent delivered a strong second quarter, significantly exceeding the high end of our guidance range with revenues of $234 million, primarily driven by accelerated MCM/biodefense contract modifications secured with the U.S. government. This performance reflects the focus, discipline and commitment of our teams, and it reinforces the strength of our mission, our portfolio and the steadiness of our multi-year plan toward transformation," said Joe Papa, CEO of Emergent. "However, alongside of these strong results, we are at a critical juncture in our turnaround and transformation, primarily stemming from our naloxone business. Today we are implementing an organizational restructuring plan and taking proactive steps to strengthen our financial foundation, align the company to the realities of the naloxone business and preserve our ability to invest in the areas that matter most for Emergent’s future. Additionally, we seek to collaborate with AI partners for bioterrorism preparedness.”

FINANCIAL HIGHLIGHTS (1)

Q2 2026 vs. Q2 2025

($ in millions, except per share amounts)Q2 2026Q2 2025% ChangeTotal Revenues$234.3 $140.9 66%Net Loss$(180.2)$(12.0)(1,402)%Net Loss per Diluted Share$(3.49)$(0.22)(1,486)%Adjusted Net Income (2)$30.9 $13.2 134%Adjusted Net Income per Diluted Share (2)$0.60 $0.24 150%Adjusted EBITDA (2)$96.5 $33.1 192%Net Loss Margin(77)%(9)% Adjusted EBITDA Margin (2) 41% 23% Gross Margin % 50% 36% Adjusted Gross Margin % (2) 58% 49%  Year to Date ("YTD") 2026 vs YTD 2025

($ in millions, except per share amounts)YTD 2026YTD 2025% ChangeTotal Revenues$390.4 $363.1 8%Net Income (Loss)$(173.4)$56.0 (410)%Net Income (Loss) per Diluted Share$(3.35)$0.99 (438)%Adjusted Net Income (2)$42.8 $55.4 (23)%Adjusted Net Income per Diluted Share (2)$0.83 $0.98 (15)%Adjusted EBITDA (2)$132.0 $112.2 18%Net Income (Loss) Margin(44)% 15% Adjusted EBITDA Margin (2) 34% 31% Gross Margin % 46% 45% Adjusted Gross Margin % (2) 56% 55%          RECENT BUSINESS UPDATES

Secured contract modification from U.S. government and completed delivery of approximately $52.7 million of ACAM2000® (Smallpox and Mpox (Vaccinia) Vaccine, Live)Executed $64.5 million for BAT® (Botulism Antitoxin Heptavalent (A, B, C, D, E, F, G) – (Equine)) contract modification with U.S. governmentSecured two new strategic manufacturing partnerships with: SAB Biotherapeutics to advance its type 1 diabetes candidate, SAB-142Substipharm Biologics to support its Japanese Encephalitis vaccine in the United States; Refinanced term loan with new $150 million facility and amended asset-backed loan facilityAnnounced partnership with British Columbia to supply NARCAN® Nasal Spray for the launch of the expanded BC Take Home Naloxone ProgramSupported National Naloxone Awareness Day to increase awareness of life-saving naloxonePartnered with professional baseball player Davis Schneider to raise awareness of NARCAN® Nasal Spray in CanadaAnnounced launch of new NARCAN® Nasal Spray Carrying Case and multipack configurations to expand opioid overdose preparedness following U.S. FDA approvals on supplemental new drug applicationsReceived Saudi Food and Drug Authority Approval for ACAM2000® (Smallpox and Mpox (Vaccinia) Vaccine, Live)Received approval from Singapore Health Sciences Authority for expanded indication of ACAM2000® (Smallpox and Mpox (Vaccinia) Vaccine, Live) to include mpoxAnnounced participation in several international preparedness conferences RESTRUCTURING UPDATES

Efforts aim to improve overall cost structure, drive efficiencies and align resourcing to the current needs of the organization; includes reduction of approximately 90 rolesCreation of a new Growth organization that integrates the capabilities of R&D, Business Development, Strategy into one function led by Stephanie Duatschek, Senior Vice President, Chief Global Strategy & Franchise Development Officer, who will assume the role of Executive Vice President, Chief Growth Officer, with responsibility for the Company’s strategic growth SECOND QUARTER 2026 FINANCIAL PERFORMANCE (1)

Revenues

The Company uses the following categories in discussing revenues:

Naloxone — comprises contributions from NARCAN® Nasal Spray and KLOXXADO® Nasal SprayAnthrax MCM — comprises contributions from CYFENDUS®, BioThrax®, ANTHRASIL®, and RaxibacumabSmallpox MCM — comprises contributions from ACAM2000®, CNJ-016® (VIGIV) and TEMBEXA®Other Products — comprises contributions from BAT®All Other Revenues — comprises revenues from the Services operating segment and contracts and grants revenues ($ in millions)Q2 2026Q2 2025$ Change% ChangeProduct sales, net: (3)    Naloxone$52.4$67.5$(15.1)(22)%Anthrax MCM 12.3 11.6 0.7 6%Smallpox MCM 101.6 40.6 61.0 150%Other Products 54.1 6.2 47.9 NMTotal Product sales, net$220.4$125.9$94.5 75%     All other revenues$13.9$15.0$(1.1)(7)%     Total revenues$234.3$140.9$93.4 66%      Product Sales, net (3)

Naloxone

For Q2 2026, revenues from Naloxone products decreased $15.1 million, or 22%, as compared with Q2 2025. The decrease was primarily attributable to lower sales of OTC NARCAN®, mostly driven by an unfavorable price-volume mix in the U.S. public interest channels, partially mitigated by increases in Canadian sales of branded NARCAN® and KLOXXADO® sales.

Anthrax MCM

For Q2 2026, revenues from Anthrax MCM products increased $0.7 million, or 6%, as compared with Q2 2025. The increase was primarily attributable to a more favorable pricing mix driven by international sales of BioThrax®. This increase was partially offset by the absence of international sales of ANTHRASIL® in the current period, compared to international sales in the prior-year period. Anthrax vaccine product sales are primarily made under annual purchase options exercised by the USG. Fluctuations in revenues result from the timing of the exercise of annual purchase options, the timing of USG purchases, the availability of governmental funding and the Company’s delivery of orders that follow.

Smallpox MCM

For Q2 2026, revenues from Smallpox MCM products increased $61.0 million, or 150%, as compared with Q2 2025. The increase was primarily attributable to higher USG sales of ACAM2000® due to timing, higher CNJ-016® (VIGIV) sales with a more favorable price and volume mix of U.S. and international sales and higher TEMBEXA® international sales due to timing. Fluctuations in revenues from Smallpox MCM result from the timing of the exercise of annual purchase options in the existing procurement contracts, the timing of USG purchases, the availability of governmental funding and the Company’s delivery of orders that follow.

Other Products

For Q2 2026, revenues from Other Product sales increased $47.9 million as compared with Q2 2025. The increase was primarily due to higher USG and international BAT® sales due to timing.

All Other Revenues

Services

For Q2 2026, revenues from Services increased $2.0 million, or 45%, as compared with Q2 2025. The increase was primarily attributable to production activity at the Company’s Winnipeg facility.

Contracts and Grants

For Q2 2026, revenues from contracts and grants decreased $3.1 million, or 29%, as compared with Q2 2025. The decrease was primarily due to lower Ebanga® related development work, reflecting timing and nature of work performed.

Operating Expenses

($ in millions)Q2 2026Q2 2025$ Change% ChangeCost of product and services sales, net$97.1$66.9$30.2 45%Research and development (“R&D”) 9.2 12.5 (3.3)(26)%Selling, general and administrative (“SG&A”) 44.6 43.7 0.9 2%Amortization of intangible assets 17.2 16.2 1.0 6%Impairment of long-lived assets 191.3 — 191.3 NMTotal operating expenses$359.4$139.3$220.1 158%           Cost of Product and Services Sales, Net

For Q2 2026, cost of product and services sales, net increased $30.2 million, or 45%, as compared with Q2 2025. The increase was driven by higher cost of MCM Product sales of $27.0 million and cost of Services of $3.3 million, partially offset by a decrease in cost of Commercial Product sales of $0.1 million.

Research and Development Expenses

For Q2 2026, R&D expenses decreased $3.3 million, or 26%, as compared with Q2 2025. The decrease was primarily due to lower project spend on Ebanga® related development work.

Selling, General and Administrative Expenses

For Q2 2026, SG&A expenses increased $0.9 million, or 2%, as compared with Q2 2025. The increase was primarily due to lower insurance reimbursement benefits recognized in the current year period compared with the prior year period, partially offset by lower compensation, marketing and administrative support expenses.

Impairment of Long-Lived Assets

For Q2 2026, impairment of long-lived assets was $191.3 million. This was the result of a non-cash impairment charge in the second quarter of 2026 related to our NARCAN® asset group within the Commercial reporting unit.

ADDITIONAL FINANCIAL INFORMATION(1)

Capital Expenditures

($ in millions)Q2 2026Q2 2025% ChangeCapital expenditures$2.1 $2.9 (28)%Capital expenditures as a % of total revenues 1% 2%          For Q2 2026, capital expenditures decreased largely due to reduced development activities across the Company’s facilities.

REPORTABLE SEGMENT INFORMATION

The Company manages the business with a focus on three operating segments: (1) a Commercial Products segment consisting of NARCAN® Nasal Spray and KLOXXADO® Nasal Spray; (2) a MCM Products segment consisting of Anthrax - MCM, Smallpox - MCM and Other products and (3) a services segment consisting of our Bioservices offerings (“Services”). Commercial Products and MCM Products are our two reportable segments. The Services operating segment no longer meets the quantitative thresholds of a reportable segment and did not meet the aggregation criteria set forth in Accounting Standards Codification 280, Segment Reporting, and as such is categorized within “All other revenues” along with “Contracts and Grants”. The Company evaluates the performance of these reportable segments based on revenues and segment adjusted gross margin, which is a non-GAAP financial measure. Segment revenue includes external customer sales but does not include inter-segment services. The Company does not allocate contracts and grants revenue, R&D, SG&A, amortization of intangible assets, interest and other income (expense) or taxes to its evaluation of the performance of these segments.

SECOND QUARTER 2026 REPORTABLE SEGMENT RESULTS

($ in millions)Commercial ProductsQuarter Ended June 30, 2026  2025 $ Change% ChangeRevenues$52.4 $67.5 $(15.1)(22)%Cost of sales 36.3  36.4  (0.1)—%Intangible asset amortization 9.4  9.4  — —%Gross margin*$6.7 $21.7 $(15.0)(69)%Gross margin %* 13% 32%  Add back:    Intangible asset amortization$9.4 $9.4   Severance and restructuring costs —  0.2   Stock-based compensation expense 0.1  —   Segment adjusted gross margin **$16.2 $31.3 $(15.1)(48)%Segment adjusted gross margin % ** 31% 46%            * Gross margin is calculated as revenues less cost of sales and intangible asset amortization. Gross margin % is calculated as gross margin divided by revenues.** Segment adjusted gross margin, which is a non-GAAP financial measure, for our Commercial Products segment is calculated as gross margin plus intangible asset amortization, severance and restructuring costs and the portion of stock-based compensation expense that is recorded as cost of sales. Segment adjusted gross margin percentage, which is a non-GAAP financial measure, is calculated as segment adjusted gross margin divided by revenues. The Company’s management utilizes segment adjusted gross margin and segment adjusted gross margin percentage for purposes of evaluating our ongoing operations and for internal planning and forecasting purposes. In calculating these measures, we began excluding stock-based compensation that is recorded as cost of sales in the first quarter of 2026, as this reflects a non-cash expenditure that is not related to segment operating performance. As reflected in the table above, we have recast our 2025 results to also reflect this adjustment. We believe that these non-GAAP operating measures, when reviewed collectively with our GAAP financial information, provide useful supplemental information to investors in assessing our operating performance.NM - Not meaningful  Cost of Commercial Products sales decreased $0.1 million to $36.3 million for the quarter ended June 30, 2026. Despite decreases in U.S. sales volumes of OTC NARCAN® compared with the prior year period, cost of sales remained substantially flat due to increased costs and volumes associated with KLOXXADO® sales and Canadian sales of branded NARCAN®.

Commercial Products gross margin decreased $15.0 million, or 69%, to $6.7 million for the quarter ended June 30, 2026. Commercial Products gross margin percentage decreased 19 percentage points to 13% for the quarter ended June 30, 2026. The decrease was largely due to an unfavorable price and volume mix of OTC NARCAN® across most U.S. sales channels, partially offset by lower product costs related to Canadian sales. Commercial Products segment adjusted gross margin in the current year period excludes the impact of intangible asset amortization of $9.4 million and the portion of stock-based compensation expense recorded as cost of sales of $0.1 million.

($ in millions)MCM ProductsQuarter Ended June 30, 2026  2025 $ Change% ChangeRevenues$168.0 $58.4 $109.6188%Cost of sales 52.8  25.8  27.0105%Intangible asset amortization 7.8  6.8  1.015%Gross margin*$107.4 $25.8 $81.6NMGross margin %* 64% 44%  Add back:    Intangible asset amortization$7.8 $6.8   Inventory step-up provision 0.2  —   Severance and restructuring benefit —  (0.4)  Stock-based compensation expense 0.7  0.3   Segment adjusted gross margin**$116.1 $32.5 $83.6NMSegment adjusted gross margin %** 69% 56%            * Gross margin is calculated as revenues less cost of sales and intangible asset amortization. Gross margin % is calculated as gross margin divided by revenues.** Segment adjusted gross margin, which is a non-GAAP financial measure, for our MCM Products segment is calculated as gross margin plus intangible asset amortization, inventory step-up provision, severance and restructuring benefit and the portion of stock-based compensation expense that is recorded as cost of sales. Segment adjusted gross margin percentage, which is a non-GAAP financial measure, is calculated as segment adjusted gross margin divided by revenues. The Company’s management utilizes segment adjusted gross margin and segment adjusted gross margin percentage for purposes of evaluating our ongoing operations and for internal planning and forecasting purposes. In calculating these measures, we began excluding stock-based compensation that is recorded as cost of sales in the first quarter of 2026, as this reflects a non-cash expenditure that is not related to segment operating performance. As reflected in the table above, we have recast our 2025 results to also reflect this adjustment. We believe that these non-GAAP operating measures, when reviewed collectively with our GAAP financial information, provide useful supplemental information to investors in assessing our operating performance.NM - Not Meaningful  Cost of MCM product sales increased $27.0 million, or 105%, to $52.8 million for the quarter ended June 30, 2026. The increase was primarily attributable to higher product sales volumes for BAT®, ACAM2000®, CNJ-016® (VIGIV), BioThrax®, and TEMBEXA®, as well as a significant non-recurring manufacturing cost related to the production of CYFENDUS®. These increases were partially offset by a decrease in cost of sales for ANTHRASIL® driven by lower sales volumes.

MCM Products gross margin increased $81.6 million to $107.4 million for the quarter ended June 30, 2026. MCM Product gross margin percentage increased 20 percentage points to 64% for the quarter ended June 30, 2026. The increase in gross margin percentage was primarily driven by a more favorable sales mix and increased sales volumes, which improved absorption of fixed manufacturing costs. These improvements were partially offset by a significant non-recurring manufacturing cost related to the production of CYFENDUS®. MCM Product segment adjusted gross margin in the current year period excludes the impacts of intangible asset amortization of $7.8 million, the portion of stock-based compensation expense recorded as cost of sales of $0.7 million and inventory step-up provision of $0.2 million.

YTD 2026 REPORTABLE SEGMENT RESULTS

($ in millions)Commercial ProductsSix Months Ended June 30, 2026  2025 $ Change% ChangeRevenues$95.3 $112.8 $(17.5)(16)%Cost of sales 63.1  60.9  2.2 4%Intangible asset amortization 18.9  18.9  — —%Gross margin*$13.3 $33.0 $(19.7)(60)%Gross margin %* 14% 29%  Add back:    Intangible asset amortization$18.9 $18.9   Severance and restructuring costs —  0.2   Stock-based compensation expense 0.1  —   Segment adjusted gross margin**$32.3 $52.1 $(19.8)(38)%Segment adjusted gross margin %** 34% 46%            * Gross margin is calculated as revenues less cost of sales and intangible asset amortization. Gross margin % is calculated as gross margin divided by revenues.** Segment adjusted gross margin, which is a non-GAAP financial measure, for our Commercial Products segment is calculated as gross margin plus intangible asset amortization, severance and restructuring costs and the portion of stock-based compensation expense that is recorded as cost of sales. Segment adjusted gross margin percentage, which is a non-GAAP financial measure, is calculated as segment adjusted gross margin divided by revenues. The Company’s management utilizes segment adjusted gross margin and segment adjusted gross margin percentage for purposes of evaluating our ongoing operations and for internal planning and forecasting purposes. In calculating these measures, we began excluding stock-based compensation that is recorded as cost of sales in the first quarter of 2026, as this reflects a non-cash expenditure that is not related to segment operating performance. As reflected in the table above, we have recast our 2025 results to also reflect this adjustment. We believe that these non-GAAP operating measures, when reviewed collectively with our GAAP financial information, provide useful supplemental information to investors in assessing our operating performance.NM - Not Meaningful  Cost of Commercial Product sales increased $2.2 million, or 4%, to $63.1 million for the six months ended June 30, 2026. The increase was primarily due higher KLOXXADO® sales and Canadian sales of branded NARCAN®, largely offset by lower sales volumes of OTC NARCAN® in the U.S.

Commercial Products gross margin decreased $19.7 million, or 60%, to $13.3 million for the six months ended June 30, 2026. Commercial Products gross margin percentage decreased 15 percentage points to 14% for the six months ended June 30, 2026. The decrease was largely due to an unfavorable price and volume mix of OTC NARCAN® across all U.S. sales channels and product mix due to the introduction of KLOXXADO®, partially offset by lower product costs related to the Canadian sales. Commercial Products segment adjusted gross margin in the current year period excludes the impact of intangible asset amortization of $18.9 million and the portion of stock-based compensation expense recorded as cost of sales of $0.1 million.

($ in millions)MCM ProductsSix Months Ended June 30, 2026  2025 $ Change% ChangeRevenues$269.8 $215.0 $54.825%Cost of sales 89.6  76.0  13.618%Intangible asset amortization 14.8  13.6  1.29%Gross margin*$165.4 $125.4 $40.032%Gross margin %* 61% 58%  Add back:    Intangible asset amortization$14.8 $13.6   Severance and restructuring benefit —  (1.2)  Inventory step-up provision 0.3  1.8   Stock-based compensation expense 1.2  0.6   Segment adjusted gross margin**$181.7 $140.2 $41.530%Segment adjusted gross margin %** 67% 65%            * Gross margin is calculated as revenues less cost of sales and intangible asset amortization. Gross margin % is calculated as gross margin divided by revenues.** Segment adjusted gross margin, which is a non-GAAP financial measure, for our MCM Products segment is calculated as gross margin plus intangible asset amortization, inventory step-up provision, severance and restructuring benefit and the portion of stock-based compensation expense that is recorded as cost of sales. Segment adjusted gross margin percentage, which is a non-GAAP financial measure, is calculated as segment adjusted gross margin divided by revenues. The Company’s management utilizes segment adjusted gross margin and segment adjusted gross margin percentage for purposes of evaluating our ongoing operations and for internal planning and forecasting purposes. In calculating these measures, we began excluding stock-based compensation that is recorded as cost of sales in the first quarter of 2026, as this reflects a non-cash expenditure that is not related to segment operating performance. As reflected in the table above, we have recast our 2025 results to also reflect this adjustment. We believe that these non-GAAP operating measures, when reviewed collectively with our GAAP financial information, provide useful supplemental information to investors in assessing our operating performance.NM - Not Meaningful  Cost of MCM product sales increased $13.6 million, or 18%, to $89.6 million for the six months ended June 30, 2026. The increase was primarily due to higher cost of sales of BAT®, CNJ-016® (VIGIV) and BioThrax®, reflecting increased sales volumes as well as increased non-recurring manufacturing costs related to production of CYFENDUS®. These increases were partially offset by lower cost of sales for ANTHRASIL® and TEMBEXA® due to lower unit sales volume.

MCM Product gross margin increased $40.0 million, or 32%, to $165.4 million for the six months ended June 30, 2026. MCM Product gross margin percentage increased 3 percentage points to 61% for the six months ended June 30, 2026. The increase in gross margin percentage was primarily due to a favorable sales volume and product mix which was weighted more heavily towards higher margin products, the margin improvements were partially offset by non-recurring manufacturing costs mentioned above. MCM Product segment adjusted gross margin in the current year period excludes the impacts of intangible asset amortization of $14.8 million, the portion of stock-based compensation expense recorded as cost of sales of $1.2 million and inventory step-up provision of $0.3 million.

2026 FINANCIAL FORECAST

The Company provides the following updated financial forecast for full year 2026, reflecting management's expectations based on the most current information available.

METRIC
($ in millions)Updated Range
(as of 08/05/2026)ActionPrevious Range
(as of 04/30/2026)Total revenues$645 - $675REVISED$720 - $760Net loss$(245) - $(225)REVISED$(30) - $(10)Adjusted net income (2)$10 - $30REVISED$45 - $65Adjusted EBITDA (2)$130 - $150REVISED$155 - $175Adjusted gross margin % (2)42% - 44%REVISED45% - 47%     Key Assumptions
($ and shares in millions)Updated Range
(as of 08/05/2026)Interest expense~$40R&D~6% of RevenuesSG&A~27% to 28% of RevenuesWeighted avg. fully diluted share count~52Stock-based compensation expense~$19Capex~$17Depreciation & amortization~$82   Q2 2026

METRIC
($ in millions)                                  Q3 2026 ForecastTotal revenues$110 - $130   FOOTNOTES

(1) All financial information included in this release is unaudited.

(2) See “Non-GAAP Financial Measures” and the “Reconciliation of Non-GAAP Financial Measures” tables for the definitions and reconciliations of Company-wide non-GAAP financial measures to the most closely related GAAP financial measures. Reconciliations of segment non-GAAP financial measures are included within the reportable segment tables. In the first quarter of 2026 we revised our calculations of these measures to exclude the impact of stock-based compensation expense, as this is a non-cash expense that is not related to our operating performance. The updated ranges for our 2026 forecast reflect this adjustment.

(3) Product sales, net are reported net of variable consideration including returns, rebates, wholesaler fees and prompt pay discounts in accordance with GAAP.

CONFERENCE CALL, PRESENTATION SUPPLEMENT AND WEBCAST INFORMATION

Company management will host a conference call at 5:00 pm eastern time today, August 5, 2026, to discuss these financial results. The conference call and presentation supplement can be accessed from the Company's website or through the following:

By phone
Advanced registration is required.
Visit https://register-conf.media-server.com/register/BI77a0454e68eb4a728e6c2ddddee54766 to register and receive an email with the dial-in number, passcode and registrant ID.

By webcast
Visit https://edge.media-server.com/mmc/p/fjwb9v5g/ 
A replay of the call can be accessed from the Emergent website.

ABOUT EMERGENT BIOSOLUTIONS INC.

At Emergent, our mission is to protect and save lives. For over 25 years, we’ve been at work preparing those entrusted with protecting public health. We deliver protective and life-saving solutions for health threats like smallpox, mpox, botulism, Ebola, anthrax and opioid overdose emergencies. To learn more about how we help prepare communities around the world for today’s health challenges and tomorrow’s threats, visit our website and follow us on LinkedIn, X, Instagram, Apple Podcasts and Spotify.

NON-GAAP FINANCIAL MEASURES

In the accompanying analysis of financial information, we sometimes use information derived from consolidated and segment financial information that may not be presented in our financial statements or prepared in accordance with generally accepted accounting principles in the United States (“GAAP”). Certain of these financial measures are considered not in conformity with GAAP (“non-GAAP financial measures”) under the United States Securities and Exchange Commission (“SEC”) rules. Specifically, we have referred to the following non-GAAP financial measures:

Adjusted Net IncomeAdjusted Net Income per Diluted ShareAdjusted EBITDAAdjusted EBITDA MarginAdjusted Gross MarginAdjusted Gross Margin %Segment Adjusted Gross MarginSegment Adjusted Gross Margin % We define Adjusted Net Income and Adjusted Net Income per Diluted Share, which are non-GAAP financial measures, as net income (loss) and net income (loss) per diluted share, respectively, excluding the impact of non-cash amortization charges, impairments, severance and restructuring costs (benefits), inventory step-up provision, acquisition and divestiture costs, loss on assets held for sale, contingent consideration milestones, changes in fair value of financial instruments, stock-based compensation expense, loss on debt extinguishment, other, net, and tax effects. In the first quarter of 2026 we revised our calculation of these measures to exclude the impact of stock-based compensation expense, as this is a non-cash expense that is not related to our operating performance. We use Adjusted Net Income for the purpose of calculating Adjusted Net Income per Diluted Share. Management uses Adjusted Net Income per Diluted Share to assess total Company operating performance on a consistent basis. We believe that these non-GAAP financial measures, when considered together with our GAAP financial results and GAAP financial measures, provide management and investors with an additional understanding of our business operating results, including underlying trends.

We define Adjusted EBITDA, which is a non-GAAP financial measure, as net income (loss) before depreciation and amortization, income taxes, total interest expense, net, impairments, inventory step-up provision, changes in fair value of financial instruments, severance and restructuring costs (benefits), acquisition and divestiture costs, loss on assets held for sale, contingent consideration milestones, stock-based compensation expense, loss on debt extinguishment, and other, net. We define Adjusted EBITDA Margin, which is a non-GAAP financial measure, as Adjusted EBITDA divided by Total Revenues. In the first quarter of 2026 we revised our calculation of these measures to exclude the impact of stock-based compensation expense, as this is a non-cash expense that is not related to our operating performance. We believe that these non-GAAP financial measures, when considered together with our GAAP financial results and GAAP financial measures, provide management and investors with a more complete understanding of our operating results, including underlying trends. In addition, EBITDA is a common alternative measure of operating performance used by many of our competitors. It is used by investors, financial analysts, rating agencies and others to value and compare the financial performance of companies in our industry, although it may be defined differently by different companies. Therefore, we also believe that this non-GAAP financial measure, considered along with corresponding GAAP financial measures, provides management and investors with additional information for comparison of our operating results with the operating results of other companies.

We define Adjusted Gross Margin, which is a non-GAAP financial measure, as Gross Margin, excluding the impact of intangible asset amortization, stock-based compensation expense, severance and restructuring costs (benefits) and inventory step-up provision. We define Adjusted Gross Margin %, which is a non-GAAP financial measure, as Adjusted Gross Margin as a percentage of Products and services sales, net. In the first quarter of 2026 we revised our calculation of these measures to exclude the impact of stock-based compensation expense, as this is a non-cash expense that is not related to our operating performance.

We define Segment Adjusted Gross Margin, which is a non-GAAP financial measure, as a segment's Gross Margin excluding the respective impact of intangible asset amortization, severance and restructuring costs (benefits), stock-based compensation expense and inventory step-up provision. We define Segment Adjusted Gross Margin %, which is a non-GAAP financial measure, as Segment Adjusted Gross Margin as a percentage of a segment's revenues. In the first quarter of 2026 we revised our calculation of these measures to exclude the impact of stock-based compensation expense, as this is a non-cash expense that is not related to segment operating performance.

Non-GAAP financial measures are not defined in the same manner by all companies and may not be comparable with other similarly titled measures of other companies. The determination of the amounts that are excluded from these non-GAAP financial measures are a matter of management judgment and depend upon, among other factors, the nature of the underlying expense or income amounts. Non-GAAP financial measures should be considered in addition to, but not as a substitute for or superior to, the information contained in our Consolidated Statements of Operations and Consolidated Statements of Cash Flows. Reconciliations of these non-GAAP financial measures to the most directly comparable GAAP financial measures are included in the financial tables accompanying this press release.

SAFE HARBOR STATEMENT

This press release includes forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, as amended. All statements, other than statements of historical fact, including statements regarding the future performance of the Company or any of our businesses, our business strategy, future operations, future financial position, future revenues and earnings, our ability to achieve the objectives of our restructuring initiatives, acquisitions and divestitures, including our future results, projected costs, prospects, plans and objectives of management, are forward-looking statements. We generally identify forward-looking statements by using words like “anticipate,” “believe,” “can,” “continue,” “could,” “estimate,” “expect,” “confident,” “commit,” “forecast,” “future,” “outlook,” “goal,” “intend,” “may,” “plan,” “position,” “possible,” “potential,” “predict,” “project,” “should,” “target,” “will,” “would,” and similar expressions or variations thereof, or the negative thereof, but these terms are not the exclusive means of identifying such statements. These forward-looking statements are based on our current intentions, beliefs, assumptions and expectations regarding future events based on information that is currently available. You should realize that if underlying assumptions prove inaccurate or unknown risks or uncertainties materialize, actual results could differ materially from our expectations. Readers are, therefore, cautioned not to place undue reliance on any forward-looking statement contained herein. Any such forward-looking statement speaks only as of the date of this press release, and, except as required by law, we do not undertake any obligation to update any forward-looking statement to reflect new information, events or circumstances.

There are a number of important factors that could cause our actual results to differ materially from those indicated by such forward-looking statements, including, among others, the availability of USG funding for contracts related to procurement of our medical countermeasures (“MCM”) products, including CYFENDUS® (Anthrax Vaccine Adsorbed (AVA) Adjuvanted), previously known as AV7909, ACAM2000® (Smallpox and Mpox (Vaccinia) Vaccine, Live), CNJ-016® (Vaccinia Immune Globulin Intravenous (Human) (VIGIV)), BAT® (Botulism Antitoxin Heptavalent (A,B,C,D,E,F,G)-(Equine)), BioThrax® (Anthrax Vaccine Adsorbed) Ebanga® (ansuvimab-zykl) and/or TEMBEXA® (brincidofovir) among others, as well as contracts related to development of medical countermeasures; our ability to meet our commitments to quality and compliance in all of our manufacturing operations; our ability to negotiate additional USG procurement or follow-on contracts for our MCM products that have expired or will be expiring; the commercial availability and impact of a generic and competitive marketplace on future sales of NARCAN® (naloxone HCL) Nasal Spray, over-the-counter NARCAN® Nasal Spray and KLOXXADO® Nasal Spray; our ability to perform under our contracts with the USG, including the timing of and specifications relating to deliveries; the ability of our contractors and suppliers to maintain compliance with current good manufacturing practices and other regulatory obligations; our ability to collect reimbursement for raw materials and payment of service fees from our Bioservices customers; the results of pending government investigations and their potential impact on our business; our ability to satisfy the conditions of our litigation settlement agreements, and the potential impact of such agreements, including the funds to resolve related litigation, on our business; our ability to comply with the operating and financial covenants required by (i) our term loan facility under the Credit Agreement, dated April 16, 2026, by and among the Company, the lenders from time to time party thereto, and OrbiMed Royalty & Credit Opportunities V, LP, as administrative agent, (ii) our revolving credit facility under a credit agreement, dated September 30, 2024, among the Company, certain subsidiary borrowers, the lenders from time to time party thereto and Wells Fargo, National Association, as Agent, and (iii) our 3.875% Senior Unsecured Notes due 2028; our ability to maintain adequate internal control over financial reporting and to prepare accurate financial statements in a timely manner; our ability to maintain sufficient cash flow from our operations to pay our substantial debt, both now and in the future; our ability to invest in our business operations as a result of our current indebtedness; the impact of our share and debt repurchase programs; the procurement of our product candidates by USG entities under regulatory authorities that permit government procurement of certain medical products prior to FDA marketing authorization, and corresponding procurement by government entities outside the United States; the success of our commercialization, marketing and manufacturing capabilities and strategy; our ability to identify and acquire companies, businesses, products or product candidates that satisfy our selection criteria; our ability to attract and retain qualified personnel; our ability to adequately secure and protect our intellectual property rights; the impact of cybersecurity incidents, including the risks from the unauthorized access, interruption, failure or compromise of our information systems or those of our business partners, collaborators or other third parties; and the accuracy of our estimates regarding future revenues, expenses, capital requirements and need for additional financing. The foregoing sets forth many, but not all, of the factors that could cause actual results to differ materially from our expectations in any forward-looking statement. In addition, other risks and uncertainties not presently known to us or that we currently believe to be immaterial could affect the accuracy of any forward-looking statements. Readers should consider this cautionary statement, as well as the risks identified in our periodic reports filed with the Securities and Exchange Commission, when evaluating our forward-looking statements.

Trademarks

Emergent®, BioThrax®, BaciThrax®, BAT®, Trobigard®, ANTHRASIL®, CNJ-016®, ACAM2000®, ​NARCAN®, CYFENDUS®, TEMBEXA® and any and all Emergent BioSolutions Inc. brands, products, services and feature names, logos and slogans are trademarks or registered trademarks of Emergent BioSolutions Inc. or its subsidiaries in the United States or other countries. All other brands, products, services and feature names or trademarks are the property of their respective owners, including KLOXXADO®, which is a registered trademark of Hikma Pharmaceuticals USA Inc.

Emergent BioSolutions Inc.
Consolidated Balance Sheets
(in millions, except per share data)
     June 30, 2026 December 31, 2025(unaudited)  ASSETS   Current assets:   Cash and cash equivalents$139.7  $205.4 Restricted cash 1.2   3.7 Accounts receivable, net 190.0   84.2 Inventories, net 303.6   343.4 Prepaid expenses and other current assets 25.4   25.8 Assets held-for-sale 6.1   — Total current assets 666.0   662.5     Property, plant and equipment, net 178.0   205.4 Intangible assets, net 261.8   436.5 Other assets 11.0   14.2 Total assets$1,116.8  $1,318.6     LIABILITIES AND STOCKHOLDERS’ EQUITY   Current liabilities:   Accounts payable$50.2  $55.6 Accrued expenses 17.1   12.2 Accrued compensation 26.2   41.8 Deferred revenue 15.0   5.0 Current tax liability 4.4   6.8 Other current liabilities 9.9   10.8 Total current liabilities 122.8   132.2     Debt 581.8   572.1 Deferred tax liability 35.4   37.8 Other liabilities 35.4   53.9 Total liabilities$775.4  $796.0     Stockholders’ equity:   Preferred stock, $0.001 par value per share; 15.0 shares authorized, no shares issued and outstanding —   — Common stock, $0.001 par value per share; 200.0 shares authorized, 61.9 and 60.9 shares issued; 51.3 and 52.1 shares outstanding, respectively. 0.1   0.1 Treasury stock, at cost, 10.7 and 8.7 common shares, respectively (270.5)  (252.6)Additional paid-in capital 951.8   942.4 Accumulated other comprehensive loss, net (6.8)  (7.5)Accumulated deficit (333.2)  (159.8)Total stockholders’ equity$341.4  $522.6 Total liabilities and stockholders’ equity$1,116.8  $1,318.6          Emergent BioSolutions Inc.
Consolidated Statements of Operations
(unaudited, in millions, except per share data)
     Three Months Ended June 30, Six Months Ended June 30, 2026   2025   2026   2025 Revenues:       Product and services sales, net$226.8  $130.3  $376.5  $339.4 Contracts and grants 7.5   10.6   13.9   23.7 Total revenues 234.3   140.9   390.4   363.1         Operating expenses:       Cost of product and services sales, net (1) 97.1   66.9   169.1   155.4 Research and development 9.2   12.5   19.7   27.6 Selling, general and administrative 44.6   43.7   91.2   96.1 Amortization of intangible assets 17.2   16.2   33.7   32.5 Impairment of long-lived assets 191.3   —   191.3   — Total operating expenses 359.4   139.3   505.0   311.6         Income (loss) from operations (125.1)  1.6   (114.6)  51.5         Other income (expense):       Interest expense (10.0)  (14.7)  (21.0)  (29.4)Loss on assets held-for-sale (10.7)  —   (10.7)  (12.2)Loss on debt extinguishment (20.5)  —   (20.5)  — Other, net —   (3.7)  13.9   66.0 Total other income (expense), net (41.2)  (18.4)  (38.3)  24.4         Income (loss) before income taxes (166.3)  (16.8)  (152.9)  75.9 Income tax provision (benefit) 13.9   (4.8)  20.5   19.9 Net income (loss)$(180.2) $(12.0) $(173.4) $56.0         Earnings (loss) per common share       Basic$(3.49) $(0.22) $(3.35) $1.03 Diluted$(3.49) $(0.22) $(3.35) $0.99         Weighted average shares outstanding       Basic 51.6   54.2   51.7   54.3 Diluted 51.6   54.2   51.7   56.7                 (1) Exclusive of intangible asset amortization          Emergent BioSolutions Inc.
Consolidated Statements of Cash Flows
(unaudited, in millions)   Six Months Ended June 30, 2026   2025 Operating Activities   Net income (loss)$(173.4) $56.0 Adjustments to reconcile net income to net cash provided by operating activities:   Stock-based compensation expense 8.8   6.1 Depreciation and amortization 47.5   48.9 Amortization of deferred financing costs 3.4   4.7 Deferred income taxes (2.4)  4.7 Noncash loss on assets held-for-sale 10.7   12.2 Change in fair value of warrant liability (8.9)  (6.6)Impairment of long-lived assets 191.3   — Loss on disposal of assets 2.0   1.3 Other 19.8   (9.1)Changes in operating assets and liabilities:   Accounts receivable (107.7)  45.2 Inventories 39.8   (26.9)Prepaid expenses and other assets (0.6)  29.2 Accounts payable (4.4)  (15.8)Accrued expenses and other liabilities 1.2   (28.3)Long-term incentive plan accrual 0.4   1.6 Accrued compensation (16.0)  (26.3)Income taxes receivable and payable, net 4.3   (1.6)Contract liabilities 6.5   (0.1)Net cash provided by operating activities 22.3   95.2 Investing Activities   Purchases of property, plant and equipment (4.5)  (6.5)Proceeds from sale of property, plant and equipment 0.2   38.2 Milestone payment from prior asset acquisition (50.4)  — Milestone proceeds from prior asset divestiture —   50.0 Purchase of convertible note receivable —   (5.0)Net cash provided by (used in) investing activities (54.7)  76.7 Financing Activities   Purchases of treasury stock (18.0)  (6.9)Proceeds from stock-based compensation activity 1.4   0.8 Taxes paid for stock-based compensation activity (3.2)  (0.7)Repayment of prior term loan facility (150.0)  — Proceeds from the issuance of debt, net of lender fees 145.5   — Debt issuance and extinguishment costs (11.5)  — Net cash used in financing activities: (35.8)  (6.8)Effect of exchange rate changes on cash, cash equivalents and restricted cash —   0.3 Net change in cash, cash equivalents and restricted cash (68.2)  165.4 Cash, cash equivalents and restricted cash, beginning of period 209.1   105.6 Cash, cash equivalents and restricted cash, end of period$140.9  $271.0 Supplemental cash flow disclosures:   Cash paid for interest$16.6  $24.8 Cash paid for income taxes, net of refunds$9.6  $16.6 Non-cash investing and financing activities:   Purchases of property, plant and equipment unpaid at period end$2.6  $2.2 Loss on extinguishment of debt$(20.5) $— Excise tax liability accrued for treasury stock purchases$0.2  $— Reconciliation of cash and cash equivalents and restricted cash:   Cash and cash equivalents$139.7  $267.3 Restricted cash 1.2   3.7 Total$140.9  $271.0          Emergent BioSolutions Inc.
Reconciliation of Non-GAAP Financial Measures
Reconciliation of Net Income (loss) and Net Income (loss) per Diluted Share to Adjusted Net Income and Adjusted Net Income per Diluted Share(1)
     ($ in millions, except per share data)
Three Months Ended June 30, Six Months Ended June 30,  2026  2025   2026  2025 SourceNet income (loss)$(180.2)$(12.0) $(173.4)$56.0  Adjustments:      Inventory step-up provision$0.2 $—  $0.3 $1.8 Cost of product and services sales, netSeverance and restructuring costs (benefits) 0.5  0.5   0.7  (0.8)Cost of product and services sales, net, SG&A and R&DStock-based compensation expense 6.9  4.6   8.8  6.1 Cost of product and services sales, net, SG&A and R&DAcquisition and divestiture costs —  —   —  0.2 SG&ANon-cash amortization charges 18.8  18.7   37.2  37.2 Amortization of intangible assets ("IA"), Other IncomeImpairments 191.3  —   191.3  — Impairment of long-lived assetsLoss on assets held-for-sale 10.7  —   10.7  12.2 Other Income (Expense)Contingent consideration milestones —  —   (5.0) (50.0)Other Income (Expense)Changes in fair value of financial instruments (0.5) 2.9   (9.0) (6.6)Other Income (Expense)Loss on debt extinguishment 20.5  —   20.5  — Other Income (Expense)Other, net —  5.0   (0.3) (2.9)Other Income (Expense)Tax effect (37.3) (6.5)  (39.0) 2.2  Total adjustments:$211.1 $25.2  $216.2 $(0.6) Adjusted net income$30.9 $13.2  $42.8 $55.4  Net income (loss) per diluted share$(3.49)$(0.22) $(3.35)$0.99  Adjustments:      Inventory step-up provision$— $—  $0.01 $0.03 Cost of product and services sales, netSeverance and restructuring costs (benefits) 0.01  0.01   0.01  (0.01)Cost of product and services sales, net, SG&A and R&DStock-based compensation expense 0.13  0.08   0.17  0.11 Cost of product and services sales, net, SG&A and R&DAcquisition and divestiture costs —  —   —  — SG&ANon-cash amortization charges 0.36  0.35   0.72  0.66 Amortization of IA, Other IncomeImpairments 3.71  —   3.70  — Impairment of long-lived assetsLoss on assets held-for-sale 0.21  —   0.21  0.22 Other Income (Expense)Contingent consideration milestones —  —   (0.10) (0.88)Other Income (Expense)Changes in fair value of financial instruments (0.01) 0.05   (0.17) (0.12)Other Income (Expense)Loss on debt extinguishment 0.40  —   0.40  — Other Income (Expense)Other, net —  0.09   (0.01) (0.05)Other Income (Expense)Tax effect (0.72) (0.12)  (0.76) 0.03  Total adjustments:$4.09 $0.46  $4.18 $(0.01) Adjusted net income per diluted share$0.60 $0.24  $0.83 $0.98  Diluted shares used in computing Adjusted net income per diluted share 51.6  54.2   51.7  56.7         (1) Amounts for fiscal year 2025 have been revised from those previously reported to reflect the exclusion of stock-based compensation expense.  Emergent BioSolutions Inc.Reconciliation of Net Income (loss) and Net Income (loss) Margin to Adjusted EBITDA and Adjusted EBITDA Margin(1)

    ($ in millions)Three Months Ended June 30, Six Months Ended June 30, 2026  2025   2026  2025 Net income (loss)$(180.2)$(12.0) $(173.4)$56.0 Adjustments:     Depreciation & amortization$24.0 $23.5  $47.5 $48.9 Income taxes 13.9  (4.8)  20.5  19.9 Total interest expense, net 9.2  13.4   19.4  27.4 Inventory step-up provision 0.2  —   0.3  1.8 Severance and restructuring costs (benefits) 0.5  0.5   0.7  (0.8)Stock-based compensation expense 6.9  4.6   8.8  6.1 Acquisition and divestiture costs —  —   —  0.2 Impairments 191.3  —   191.3  — Loss on assets held-for-sale 10.7  —   10.7  12.2 Contingent consideration milestones —  —   (5.0) (50.0)Changes in fair value of financial instruments (0.5) 2.9   (9.0) (6.6)Loss on debt extinguishment 20.5  —   20.5  — Other, net —  5.0   (0.3) (2.9)Total adjustments$276.7 $45.1  $305.4 $56.2 Adjusted EBITDA$96.5 $33.1  $132.0 $112.2       Total revenues$234.3 $140.9  $390.4 $363.1       Net income (loss) margin(77)%(9)% (44)% 15%Adjusted EBITDA margin 41% 23%  34% 31%      (1) Amounts for fiscal year 2025 have been revised from those previously reported to reflect the exclusion of stock-based compensation expense.  Emergent BioSolutions Inc.Reconciliations of Total Revenues to Product and Services Sales, Net and of Gross Margin and Gross Margin %
to Adjusted Gross Margin and Adjusted Gross Margin %(1)

     Three Months Ended June 30, Six Months Ended June 30,($ in millions) 2026  2025   2026  2025 Total revenues$234.3 $140.9  $390.4 $363.1 Contracts and grants 7.5  10.6   13.9  23.7 Product and services sales, net$226.8 $130.3  $376.5 $339.4       Cost of product and services sales, net 97.1  66.9   169.1  155.4 Intangible asset amortization 17.2  16.2   33.7  32.5 Gross margin$112.5 $47.2  $173.7 $151.5 Gross margin % 50% 36%  46% 45%Add back:     Intangible asset amortization$17.2 $16.2  $33.7 $32.5 Stock-based compensation expense 0.9  0.3   1.4  0.6 Severance and restructuring costs (benefits) 0.1  (0.1)  0.1  (1.0)Inventory step-up provision 0.2  —   0.3  1.8 Adjusted gross margin$130.9 $63.6  $209.2 $185.4 Adjusted gross margin % 58% 49%  56% 55%      (1) Amounts for fiscal year 2025 have been revised from those previously reported to reflect the exclusion of stock-based compensation expense.  Emergent BioSolutions Inc.
Reconciliation of Net Loss Forecast to Adjusted Net Income Forecast
   ($ in millions)2026 Full Year ForecastSourceNet loss$(245) - $(225) Adjustments:  Inventory step-up provision$4Cost of products and services, netSeverance and restructuring costs11Cost of products and services, net, SG&A and R&DStock-based compensation expense19COGS, R&D and SGANon-cash amortization charges63Amortization of IA and Other Income (Expense)Impairments191Impairment of long-lived assetsLoss on assets held-for-sale11Other Income (Expense)Contingent consideration milestones(10)Other Income (Expense)Changes in fair value of financial instruments(9)Other Income (Expense)Loss on debt extinguishment21Other Income (Expense)Tax effect(46) Total adjustments:$255 Adjusted net income$10 - $30     Reconciliation of Net Loss Forecast to Adjusted EBITDA Forecast
  ($ in millions)2026 Full Year ForecastNet loss$(245) - $(225)Adjustments: Depreciation & amortization$82Income taxes15Total interest expense, net40Inventory step-up provision4Severance and restructuring costs11Stock-based compensation expense19Impairments191Loss on assets held-for-sale11Contingent consideration milestones(10)Changes in fair value of financial instruments(9)Loss on debt extinguishment21Total adjustments$375Adjusted EBITDA$130 - $150   Emergent BioSolutions Inc.Reconciliations of Forecasted Total Revenues to Forecasted Product and Services Sales, Net and of Forecasted Gross Margin and Gross Margin % to Forecasted Adjusted Gross Margin and Adjusted Gross Margin %

  ($ in millions)2026 Full Year Forecast Total revenues$645 - $675Contracts & Grants$(25) - $(25)Product and services sales, net$620 - $650  Cost of product and services sales, net$365 - $369Intangible asset amortization55Gross margin$200 - $226Gross margin %32% - 35%  Add back: Intangible asset amortization$55
Inventory step-up provision4Severance and restructuring costs1Stock-based compensation expense3Adjusted gross margin$263 - $289Adjusted gross margin %42% - 44%
2026-06-29 15:09 2mo ago
2026-06-29 09:13 2mo ago
Emergent BioSolutions získala zakázku za 52,7 milionu USD
EBS Emergent Biosolutions
FMP Stock News 92
Original source text
GAITHERSBURG, Md., June 29, 2026 (GLOBE NEWSWIRE) -- Emergent BioSolutions (NYSE:EBS) today announced it has been awarded a contract modification valued at $52.7 million from the Administration for Strategic Preparedness and Response (ASPR) at the United States Department of Health and Human Services to supply ACAM2000® (Smallpox and Mpox (Vaccinia) Vaccine, Live) vaccine, ancillaries as well as diluent replacement lots for smallpox preparedness and response needs. Deliveries are expected to begin this month.

“This new contract modification for ACAM2000® underscores the U.S. government’s continued focus on biodefense preparedness and reflects Emergent’s longstanding role to collaborate and help protect civilians and warfighters against potential smallpox and mpox threats,” said Paul Williams, senior vice president, head of products business, global government & public affairs at Emergent. “In this increasingly dangerous world, we are proud to continue supporting the U.S. government as they continue to take critical, proactive steps on biodefense preparedness.”

This award follows Emergent’s recent announcements that the Saudi Food and Drug Authority has approved ACAM2000® for immunization against smallpox and mpox in high-risk individuals and that Singapore’s Health Sciences Authority has approved an expanded indication for ACAM2000® to include prevention of mpox disease in adults determined to be at high risk for mpox infection.

Experts consider smallpox to be a credible bioterror threat,  with potential health, economic and national security implications due to its mortality rate.1  Emergent specializes in developing, manufacturing and delivering medical countermeasures to the U.S. government and allies around the world to support health preparedness and help protect the public from potential threats like smallpox, mpox, Ebola, anthrax and botulism.

This contract modification is under Emergent’s existing 10-year contract (75A50119C00071) with ASPR.

Indication and Select Important Safety Information for ACAM2000® (Smallpox and Mpox (Vaccinia) Vaccine, Live)
Indication
ACAM2000® is indicated for active immunization for the prevention of smallpox and mpox disease in individuals determined to be at high risk for smallpox or mpox infection.

Important Safety Information
Warning: Serious Complications
Myocarditis and pericarditis (suspect cases observed at a rate of 5.7 per 1000 primary vaccinees (95% CI: 1.9-13.3)), encephalitis, encephalomyelitis, encephalopathy, progressive vaccinia, generalized vaccinia, severe vaccinial skin infections, erythema multiforme major (including STEVENS-JOHNSON SYNDROME), eczema vaccinatum resulting in permanent sequelae or death, accidental eye infection (ocular vaccinia) which can cause ocular complications that may lead to blindness, and fetal death, have occurred following either primary vaccination or revaccination with ACAM2000® or other live vaccinia virus vaccines that were used historically.

Contraindications
Do not administer ACAM2000® to individuals with severe immunodeficiency. These individuals may include persons who are undergoing bone marrow transplantation or persons with primary or acquired immunodeficiency states who require isolation.

Warnings and Precautions
Serious complications that may follow either primary or revaccination with ACAM2000® include myocarditis and/or pericarditis, ischemic heart disease and non-ischemic dilated cardiomyopathy, encephalitis, encephalomyelitis, encephalopathy, progressive vaccinia (vaccinia necrosum), generalized vaccinia, severe vaccinial skin infections, erythema multiforme major (including Stevens-Johnson syndrome), eczema vaccinatum, fetal vaccinia, fetal death, and accidental eye infection (ocular vaccinia) that may lead to blindness. ACAM2000® is a live vaccinia virus that can be transmitted to persons who have close contact with the vaccinee and the risks in contacts are the same as those stated for vaccinees.

Adverse Reactions
Common adverse reactions include inoculation site signs and symptoms, lymphadenitis, and constitutional symptoms, such as malaise, fatigue, fever, myalgia, and headache.
To report Suspected Adverse Reactions, contact Emergent BioSolutions at 1-877-246-8472 (U.S.), 1-800-768-2304 (Canada), or [email protected]; or VAERS at 1-800-822-7967 or https://vaers.hhs.gov.

Please see the full Prescribing Information for ACAM2000® for complete Boxed Warning and safety information.

About Emergent BioSolutions
At Emergent, our mission is to protect and save lives. For over 25 years, we’ve been at work preparing those entrusted with protecting public health. We deliver protective and life-saving solutions for health threats like smallpox, mpox, botulism, Ebola, anthrax and opioid overdose emergencies. To learn more about how we help prepare communities around the world for today’s health challenges and tomorrow’s threats, visit our website and follow us on LinkedIn, X, Instagram, Apple Podcasts and Spotify. 

Safe Harbor Statement 
This press release includes forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. All statements, other than statements of historical fact, including statements regarding the expected timing for delivery of the ACAM2000® vaccine, are forward-looking statements. We generally identify forward-looking statements by using words like “anticipate,” “believe,” “continue,” “could,” “estimate,” “expect,” “forecast,” “future,” “goal,” “intend,” “may,” “plan,” “position,” “possible,” “potential,” “predict,” “project,” “should,” “target,” “will,” “would,” and similar expressions or variations thereof, or the negative thereof, but these terms are not the exclusive means of identifying such statements. Forward-looking statements are based on our current intentions, beliefs, and expectations regarding future events based on information that is currently available. We cannot guarantee that any forward-looking statement will be accurate. Readers should realize that if underlying assumptions prove inaccurate or if known or unknown risks or uncertainties materialize, actual results could differ materially from our expectations. Readers are, therefore, cautioned not to place undue reliance on any forward-looking statements. Any forward-looking statement speaks only as of the date of this press release, and, except as required by law, we do not undertake any obligation to update any forward-looking statement to reflect new information, events, or circumstances. Readers should consider this cautionary statement, as well as the risk factors identified in our periodic reports filed with the U.S. Securities and Exchange Commission, when evaluating our forward-looking statements. 

Investor Contact:
Richard S. Lindahl
Executive Vice President, CFO
[email protected]

Media Contact:
Assal Hellmer
Vice President, Communications
[email protected]

1Smallpox as a Weapon for Bioterrorism