Savara Announces Chief Medical Officer (CMO) Transition
-- Yasmine Wasfi, M.D., Ph.D., FCCP Promoted to CMO, Effective Immediately --
-- CMO Ray Pratt, M.D., FACP to Transition to Senior Medical Advisor --
“We are pleased to promote Dr. Wasfi to CMO,” said Matt Pauls, J.D., M.B.A., Chair and Chief Executive Officer, Savara. “Dr. Wasfi is a pulmonologist with more than two decades of healthcare experience, spanning both biotech and large pharma. She has a strong track record progressing and driving the development strategy for investigational therapies within the respiratory and immunology therapeutic areas and her leadership and relentless commitment to the autoimmune pulmonary alveolar proteinosis, or autoimmune PAP, patient community has been instrumental in helping advance the MOLBREEVI* program. We appreciate Dr. Wasfi’s contributions to date and look forward to the insights and direction she will bring in her new role.”
Pauls continued, “Having contributed to many regulatory applications over the span of his 35 years in drug development, we are grateful to benefit from Dr. Pratt’s experience and thank him for his invaluable contributions in advancing the MOLBREEVI program. We are fortunate to continue with his guidance as a Senior Medical Advisor.”
“I’d like to congratulate Dr. Wasfi on her promotion,” said Ray Pratt, M.D., FACP, CMO, Savara. “She brings significant experience in biopharmaceuticals to this role and has already made important contributions to our clinical development and regulatory efforts. It’s been a privilege to lead the MOLBREEVI clinical program through numerous late-stage milestones as we work to bring the first and only approved therapy for autoimmune PAP to market in the
Dr. Wasfi is a seasoned professional within clinical research and drug development of both large and small molecule novel therapeutics. Her clinical development work includes respiratory drug development and late-phase immunology clinical development. Dr. Wasfi has held roles of increasing responsibility within large pharmaceutical and smaller biotech companies, including Amicus Therapeutics, Johnson & Johnson, and Merck. She received a B.A. in Biology from the University of
Savara is a clinical stage biopharmaceutical company focused on rare respiratory diseases. Our lead program, MOLBREEVI*, is a recombinant human granulocyte-macrophage colony-stimulating factor (GM-CSF) in Phase 3 development for autoimmune pulmonary alveolar proteinosis (autoimmune PAP). MOLBREEVI is delivered via a proprietary investigational eFlow® Nebulizer System (PARI Pharma GmbH) specifically developed for inhalation of MOLBREEVI. Our management team has significant experience in rare respiratory diseases and pulmonary medicine, identifying unmet needs, and effectively advancing product candidates to approval and commercialization. More information can be found at www.savarapharma.com and LinkedIn.
*MOLBREEVI is the FDA and EMA conditionally accepted trade name for molgramostim inhalation solution. It is not approved in any indication. MOLBREEVI is a trademark of Savara Inc.
Forward-Looking Statements
Savara cautions you that statements in this press release that are not a description of historical fact are forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Forward-looking statements may be identified by the use of words referencing future events or circumstances such as “expect,” “intend,” “plan,” “anticipate,” “believe,” and “will,” among others. Such statements include, but are not limited to, statements related to the potential for MOLBREEVI to be the first and only approved therapy for autoimmune PAP on the market in the
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Media and Investor Relations Contact
Savara Inc.
Temre Johnson, Executive Director, Corporate Affairs
ir@savarapharma.com
Source: Savara Inc.