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Regeneron Donates Ebola Treatment for Use in Countries Most at Risk of Outbreaks

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Regeneron Pharmaceuticals (NASDAQ: REGN) has announced a significant humanitarian initiative, pledging to donate up to 500 doses of Inmazeb®, their FDA-approved Ebola treatment, to the World Health Organization (WHO). The donation targets low and lower-middle income countries most at risk of Ebola outbreaks.

Inmazeb®, which combines atoltivimab, maftivimab, and odesivimab-ebgn, was the first FDA-approved treatment for Orthoebolavirus zairense (Zaire ebolavirus). The company is currently expediting supplies to the Democratic Republic of Congo (DRC) to address an ongoing outbreak. Through June 2025, 266 patients have received treatment under Regeneron's compassionate use protocol.

Regeneron Pharmaceuticals (NASDAQ: REGN) ha annunciato una significativa iniziativa umanitaria, impegnandosi a donare fino a 500 dosi di Inmazeb®, loro trattamento contro l’Ebolavirus approvato dalla FDA, all’Organizzazione mondiale della sanità (OMS). La donazione è rivolta ai paesi a reddito basso e basso-medio tra i più a rischio di focolai di Ebola.

Inmazeb®, che combina atoltivimab, maftivimab e odesivimab-ebgn, è stato il primo trattamento approvato dalla FDA per Ortov Ebola zairense (Ebolavirus di Zaire). L’azienda sta attualmente accelerando le forniture nella Repubblica Democratica del Congo (RDC) per affrontare un focolaio in corso. Fino a giugno 2025, 266 pazienti hanno ricevuto trattamento nell’ambito del protocollo di uso compassionevole di Regeneron.

Regeneron Pharmaceuticals (NASDAQ: REGN) ha anunciado una importante iniciativa humanitaria, comprometida a donar hasta 500 dosis de Inmazeb®, su tratamiento contra la fiebre hemorrágica Ebola aprobado por la FDA, a la Organización Mundial de la Salud (OMS). La donación está dirigida a países de ingresos bajos y bajos‑medios con mayor riesgo de brotes de Ebola.

Inmazeb®, que combina atoltivimab, maftivimab y odesivimab-ebgn, fue el primer tratamiento aprobado por la FDA para el ortoebolavirus zairense (virus de Ebola de Zaire). La empresa está acelerando actualmente el suministro a la República Democrática del Congo (RDC) para hacer frente a un brote en curso. Hasta junio de 2025, 266 pacientes han recibido tratamiento bajo el protocolo de uso compasivo de Regeneron.

Regeneron Pharmaceuticals (NASDAQ: REGN)가 WHO(세계보건기구)에 최대 500회 분의 Inmazeb®를 기부하는 중요한 인도적 이니셔티브를 발표했습니다. 이 기부는 에볼라 발생이 가장 우려되는 저소득 및 중저소득 국가를 대상으로 합니다.

Inmazeb®는 아톨티비맙(atoltivimab), 마프티비맙(maftivimab), 오데시비맙-에브그(odesivimab-ebgn)를 결합한 치료제로, FDA 승인을 받은 최초의 치료제로 알려진 오르토에볼라바이러스 제라엔스(제어 더비 에볼라바이러스) 치료제였습니다. 현재 이 회사는 진행 중인 발병에 대응하기 위해 콩고민주공화국( RDC)으로의 공급을 가속하고 있습니다. 2025년 6월까지 266명의 환자가 Regeneron의 연민적 사용(protocol) 절차로 치료를 받았습니다.

Regeneron Pharmaceuticals (NASDAQ: REGN) a annoncé une initiative humanitaire majeure, s’engageant à faire don jusqu’à 500 doses d’Inmazeb®, leur traitement contre l’Ebola approuvé par la FDA, à l’Organisation mondiale de la Santé (OMS). Le don vise les pays à revenu faible et intermédiaire inférieur les plus exposés aux flambées d’Ebola.

Inmazeb®, qui associe l’atalitivimab, le maftivimab et l’odesivimab-ebgn, a été le premier traitement approuvé par la FDA pour l’Orthoebolavirus zairense (Ebola de Zaire). L’entreprise accélère actuellement les livraisons en République démocratique du Congo (RDC) pour faire face à une épidémie en cours. D’ici juin 2025, 266 patients ont reçu un traitement dans le cadre du protocole d’utilisation compassionate de Regeneron.

Regeneron Pharmaceuticals (NASDAQ: REGN) hat eine bedeutende humanitäre Initiative angekündigt und sich verpflichtet, bis zu 500 Dosen Inmazeb®, ihrer von der FDA zugelassenen Behandlung gegen Ebola, der Weltgesundheitsorganisation (WHO) zu spenden. Die Spende richtet sich an Länder mit niedrigem und unteren mittleren Einkommen, die am stärksten von Ebola-Ausbrüchen bedroht sind.

Inmazeb®, das aus Atoltivimab, Maftivimab und Odesivimab-ebgn besteht, war die erste FDA-zugelassene Behandlung für das Orthoebolavirus zairense (Zaire-Ebolavirus). Das Unternehmen beschleunigt derzeit die Versorgung in der Demokratischen Republik Kongo (DRK), um einen laufenden Ausbruch zu bekämpfen. Bis Juni 2025 haben 266 Patienten Behandlung im Rahmen des Regeneron‑Mitgefühl‑Protokolls erhalten.

Regeneron Pharmaceuticals (NASDAQ: REGN) أعلنت عن مبادرة إنسانية كبرى، وتتعهّد بالتبرع بما يصل إلى 500 جرعة من Inmazeb®، علاج الإيبولا المعتمد من FDA، إلى منظمة الصحة العالمية (WHO). يستهدف التبرع الدول منخفضة الدخل والدخل الأدنى المتوسط الأشدّ عرضة لحدوث تفشيات Ebola.

Inmazeb®، الذي يجمع بين atoltivimab وmaftivimab وodesivimab-ebgn، هو أول علاج معتمد من FDA لـ Orthoebolavirus zairense (إيبولا زاعري). تعمل الشركة حاليًا على تسريع الإمدادات إلى جمهورية الكونغو الديمقراطية (DRC) لمكافحة تفشٍ جارٍ. حتى يونيو 2025، تلقّى 266 مريضًا العلاج بموجب بروتوكول الاستخدام العطوف من Regeneron.

Regeneron Pharmaceuticals(纳斯达克股票代码:REGN)宣布了一项重大的人道主义倡议,承诺向世界卫生组织(WHO)捐赠多达 500剂 Inmazeb®,这是他们获FDA批准的伊波拉治疗药物。捐赠对象为最易发生埃博拉疫情的低收入及中低收入国家。

Inmazeb® 由 atoltivimab、maftivimab 与 odesivimab-ebgn 组成,是 首个获FDA批准的治疗,针对奥托埃博拉病毒(Zaire Ebola virus)。公司正加快向刚果民主共和国(DRC)提供药物,以应对正在爆发的疫情。至2025年6月,已有 266名患者 在 Regeneron 的同情用药计划下接受治疗。

Positive
  • First FDA-approved treatment for deadly Ebola virus with up to 90% untreated fatality rate
  • Demonstrates successful application of VelociSuite® technology for rapid response to public health emergencies
  • Expanding global access through WHO partnership and compassionate use program
Negative
  • None.

Inmazeb® (atoltivimab, maftivimab, and odesivimab-ebgn) was the first treatment approved by the U.S. Food and Drug Administration (FDA) for Orthoebolavirus zairense, also known as Zaire ebolavirus

Supply is being rushed to Democratic Republic of Congo (DRC) to help with the current outbreak

TARRYTOWN, N.Y., Sept. 19, 2025 (GLOBE NEWSWIRE) -- Regeneron Pharmaceuticals, Inc. (NASDAQ: REGN) today announced that it will donate up to 500 doses of Inmazeb® (atoltivimab, maftivimab, and odesivimab-ebgn), an Ebola treatment for the infection caused by Orthoebolavirus zairense, to the World Health Organization (WHO) for exclusive use by governments of low- and lower-middle income countries.1 The donation ensures this life-saving treatment continues to be available and free for people living in countries most at risk for Ebola outbreaks, and follows Regeneron’s delivery of an Inmazeb stockpile to the U.S. Government as part of the U.S. Department of Health and Human Services (HHS) efforts to enhance national preparedness for public health emergencies.

“Ebola is a notoriously dangerous and highly contagious disease, with a fatality rate of up to 90 percent when untreated,” said Leonard S. Schleifer, M.D., Ph.D., Board co-Chair, President and Chief Executive Officer of Regeneron. “During the 2018 outbreak, Regeneron changed the world’s approach to Ebola by applying our innovative VelociSuite® technology and rapid response protocols to develop Inmazeb, the first FDA-approved treatment for this deadly disease. Our donation advances our corporate responsibility goal of breaking down barriers to patient access and will benefit the most vulnerable people. We thank the world-class scientists, government and public health leaders, and courageous healthcare providers whose collaboration made this possible.”

Alongside the WHO supply agreement announced today, Regeneron is rushing Inmazeb treatments to the Democratic Republic of the Congo (DRC) for use in the current outbreak. Since 2018, Regeneron has worked with public health agencies and non-governmental organizations to rapidly offer Inmazeb at no cost under a compassionate use protocol to any country experiencing an Orthoebolavirus zairense outbreak, including the DRC and Guinea. Through June 2025, 266 patients have received treatment.  

About Inmazeb
Inmazeb is approved by the U.S. FDA for the treatment of infection caused by Orthoebolavirus zairense (also known as Zaire ebolavirus) in adult and pediatric patients, including neonates born to a mother who is RT-PCR positive for Orthoebolavirus zairense infection.

Inmazeb was created using Regeneron's VelocImmune® platform and associated VelociSuite® technologies. The treatment consists of three monoclonal antibodies that help neutralize the Ebola virus by blocking its ability to invade a patient’s cells and/or enlisting other immune cells to target infected cells and remove them from the body.

The safety and efficacy of Inmazeb was established through the 681-patient PALM Trial, which was independently conducted by the WHO, the National Institutes of Health (NIH) and the Institut National de Recherche Biomédicale (INRB) during the 2018 DRC outbreak. In 2019, as reported in the New England Journal of Medicine, the PALM Trial was stopped early following a pre-specified interim analysis that showed the superiority of Inmazeb in preventing death versus two other investigational treatments.

Inmazeb was approved by the FDA in 2020, and in 2022, WHO published its first guidelines for Ebola virus therapeutics, which strongly recommends the use of Inmazeb and calls on the global community to engage all possible mechanisms to improve access to life-saving Ebola medicines. In 2023, Inmazeb was added to the WHO Essential Medicines List and became the first and only Ebola treatment to be prequalified by the WHO, certifying that the medicine meets the organization’s standards for quality, safety and efficacy. In addition to the supply channels established in the U.S. and low- and lower-middle income countries, Regeneron has also worked with governments in higher- and middle-income countries to establish Inmazeb stockpiles.

Inmazeb was developed in collaboration and with federal funds from the Biomedical Advanced Research and Development Authority (BARDA), part of the Office of the Assistant Secretary for Preparedness and Response within HHS, under ongoing USG Contract Nos. HHSO100201700016C and HHSO100201500013C.

IMPORTANT SAFETY INFORMATION AND INDICATION
WARNINGS AND PRECAUTIONS

Hypersensitivity Reactions Including Infusion-Associated Events: Hypersensitivity reactions including infusion-associated events have been reported during and post-infusion with INMAZEB. These may include acute, life-threatening reactions during and after the infusion. Monitor all patients for signs and symptoms including, but not limited to, hypotension, chills and elevation of fever, during and following INMAZEB infusion. In the case of severe or life-threatening hypersensitivity reactions, discontinue the administration of INMAZEB immediately and administer appropriate emergency care.

Infusion could not be completed in 1% of subjects who received INMAZEB due to infusion-associated adverse events. The rate of infusion of INMAZEB may be slowed or interrupted if the patient develops any signs of infusion-associated events or other adverse events.

ADVERSE REACTIONS: 
The most common adverse events reported in at least 20% of subjects who received INMAZEB were pyrexia (or elevation in fever), chills, tachycardia, tachypnea and vomiting. The evaluation of adverse events in subjects who received INMAZEB may have been confounded by the signs and symptoms of the underlying Orthoebolavirus zairense infection.

DRUG INTERACTIONS:  INMAZEB may reduce the efficacy of live vaccine therefore, avoid the concurrent administration of a live vaccine during treatment with INMAZEB. The interval between live vaccination following initiation of INMAZEB therapy should be in accordance with current vaccination guidelines. The efficacy of INMAZEB among subjects who reported receipt of a recombinant live vaccine prior to their enrollment in the PALM clinical trial was similar to subjects who did not receive a vaccine.

INDICATION
INMAZEB is indicated for the treatment of infection caused by Orthoebolavirus zairense in adult and pediatric patients, including neonates born to a mother who is RT-PCR positive for Orthoebolavirus zairense infection.

Limitations of Use: The efficacy of INMAZEB has not been established for other species of the Orthoebolavirus and Orthomarburgvirus genera. Orthoebolavirus zairense can change over time, and factors such as emergence of resistance, or changes in viral virulence could diminish the clinical benefit of antiviral drugs. Consider available information on drug susceptibility patterns for circulating Orthoebolavirus zairense strains when deciding whether to use INMAZEB.

Please see accompanying full Prescribing Information

About Regeneron
Regeneron (NASDAQ: REGN) is a leading biotechnology company that invents, develops and commercializes life-transforming medicines for people with serious diseases. Founded and led by physician-scientists, our unique ability to repeatedly and consistently translate science into medicine has led to numerous approved treatments and product candidates in development, most of which were homegrown in our laboratories. Our medicines and pipeline are designed to help patients with eye diseases, allergic and inflammatory diseases, cancer, cardiovascular and metabolic diseases, neurological diseases, hematologic conditions, infectious diseases, and rare diseases.

Regeneron pushes the boundaries of scientific discovery and accelerates drug development using our proprietary technologies, such as VelociSuite®, which produces optimized fully human antibodies and new classes of bispecific antibodies. We are shaping the next frontier of medicine with data-powered insights from the Regeneron Genetics Center® and pioneering genetic medicine platforms, enabling us to identify innovative targets and complementary approaches to potentially treat or cure diseases.

For more information, please visit www.Regeneron.com or follow Regeneron on LinkedInInstagramFacebook or X.

Forward-Looking Statements and Use of Digital Media 
This press release includes forward-looking statements that involve risks and uncertainties relating to future events and the future performance of Regeneron Pharmaceuticals, Inc. (“Regeneron” or the “Company”), and actual events or results may differ materially from these forward-looking statements. Words such as “anticipate,” “expect,” “intend,” “plan,” “believe,” “seek,” “estimate,” variations of such words, and similar expressions are intended to identify such forward-looking statements, although not all forward-looking statements contain these identifying words. These statements concern, and these risks and uncertainties include, among others, the nature, timing, and possible success and therapeutic applications of products marketed or otherwise commercialized by Regeneron and/or its collaborators or licensees (collectively, “Regeneron’s Products”) and product candidates being developed by Regeneron and/or its collaborators or licensees (collectively, “Regeneron’s Product Candidates”) and research and clinical programs now underway or planned, including without limitation Inmazeb® (atoltivimab, maftivimab, and odesivimab-ebgn) for the treatment of infection caused by Orthoebolavirus zairense (also known as Zaire ebolavirus); uncertainty of the utilization, market acceptance, and commercial success of Regeneron’s Products (such as Inmazeb) and Regeneron’s Product Candidates and the impact of studies (whether conducted by Regeneron or others and whether mandated or voluntary), including the studies discussed or referenced in this press release, on any of the foregoing; the likelihood, timing, and scope of possible regulatory approval and commercial launch of Regeneron’s Product Candidates and new indications for Regeneron’s Products; the ability of Regeneron’s collaborators, licensees, suppliers, or other third parties (as applicable) to perform manufacturing, filling, finishing, packaging, labeling, distribution, and other steps related to Regeneron’s Products and Regeneron’s Product Candidates; the ability of Regeneron to manage supply chains for multiple products and product candidates and risks associated with tariffs and other trade restrictions; safety issues resulting from the administration of Regeneron’s Products (such as Inmazeb) and Regeneron’s Product Candidates in patients, including serious complications or side effects in connection with the use of Regeneron’s Products and Regeneron’s Product Candidates in clinical trials; determinations by regulatory and administrative governmental authorities which may delay or restrict Regeneron’s ability to continue to develop or commercialize Regeneron’s Products and Regeneron’s Product Candidates; ongoing regulatory obligations and oversight impacting Regeneron’s Products, research and clinical programs, and business, including those relating to patient privacy; the availability and extent of reimbursement or copay assistance for Regeneron’s Products from third-party payors and other third parties, including private payor healthcare and insurance programs, health maintenance organizations, pharmacy benefit management companies, and government programs such as Medicare and Medicaid; coverage and reimbursement determinations by such payors and other third parties and new policies and procedures adopted by such payors and other third parties; changes in laws, regulations, and policies affecting the healthcare industry; competing drugs and product candidates that may be superior to, or more cost effective than, Regeneron’s Products and Regeneron’s Product Candidates (including biosimilar versions of Regeneron’s Products); the extent to which the results from the research and development programs conducted by Regeneron and/or its collaborators or licensees may be replicated in other studies and/or lead to advancement of product candidates to clinical trials, therapeutic applications, or regulatory approval; unanticipated expenses; the costs of developing, producing, and selling products; the ability of Regeneron to meet any of its financial projections or guidance and changes to the assumptions underlying those projections or guidance; the potential for any license, collaboration, or supply agreement, including Regeneron’s agreements with Sanofi and Bayer (or their respective affiliated companies, as applicable), to be cancelled or terminated; the impact of public health outbreaks, epidemics, or pandemics on Regeneron's business; and risks associated with litigation and other proceedings and government investigations relating to the Company and/or its operations (including the pending civil proceedings initiated or joined by the U.S. Department of Justice and the U.S. Attorney's Office for the District of Massachusetts), risks associated with intellectual property of other parties and pending or future litigation relating thereto (including without limitation the patent litigation and other related proceedings relating to EYLEA® (aflibercept) Injection), the ultimate outcome of any such proceedings and investigations, and the impact any of the foregoing may have on Regeneron’s business, prospects, operating results, and financial condition. A more complete description of these and other material risks can be found in Regeneron’s filings with the U.S. Securities and Exchange Commission, including its Form 10-K for the year ended December 31, 2024 and its Form 10-Q for the quarterly period ended June 30, 2025. Any forward-looking statements are made based on management’s current beliefs and judgment, and the reader is cautioned not to rely on any forward-looking statements made by Regeneron. Regeneron does not undertake any obligation to update (publicly or otherwise) any forward-looking statement, including without limitation any financial projection or guidance, whether as a result of new information, future events, or otherwise.

Regeneron uses its media and investor relations website and social media outlets to publish important information about the Company, including information that may be deemed material to investors. Financial and other information about Regeneron is routinely posted and is accessible on Regeneron's media and investor relations website (https://investor.regeneron.com) and its LinkedIn page (https://www.linkedin.com/company/regeneron-pharmaceuticals).

Regeneron Contacts:

Media Relations
Alexandra Bowie
Tel: +1 (914) 847-3407
Alexandra.Bowie@regeneron.com  

Investor Relations
Mark Hudson
Tel: +1 914-847-3482
mark.hudson@regeneron.com
 

 



1 As defined by the World Bank based on gross national income per capita.


FAQ

What is Regeneron's Inmazeb and what was it approved for?

Inmazeb® is the first FDA-approved treatment for Orthoebolavirus zairense (Zaire ebolavirus), combining three antibodies: atoltivimab, maftivimab, and odesivimab-ebgn.

How many Inmazeb doses is REGN donating to WHO in 2025?

Regeneron is donating up to 500 doses of Inmazeb® to the World Health Organization for use in low and lower-middle income countries.

How many patients have received Regeneron's Ebola treatment through June 2025?

Through June 2025, 266 patients have received Inmazeb treatment under Regeneron's compassionate use protocol.

What is the fatality rate of untreated Ebola infections?

According to the press release, Ebola has a fatality rate of up to 90 percent when left untreated.

Which countries will receive Regeneron's donated Ebola treatment?

The donation is exclusively for low and lower-middle income countries, with immediate supplies being rushed to the Democratic Republic of Congo (DRC) for their current outbreak.
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