WALTHAM, Mass., Aug. 29, 2022 (GLOBE NEWSWIRE) — Dyne Therapeutics, Inc. (Nasdaq: DYN), a clinical-stage muscle disease company focused on advancing innovative life-transforming therapeutics for people living with genetically driven diseases, today announced the appointment of Francesco Bibbiani, M.D., as senior vice president, head of development. Dr. Bibbiani brings more than two decades of experience across development, including a focus on rare neuromuscular diseases as well as Duchenne muscular dystrophy (DMD).
“We are excited to welcome Francesco to Dyne’s development team at this important moment for our company, as our co-lead programs enter global clinical trials,” said Wildon Farwell, M.D., MPH, chief medical officer of Dyne. “Francesco brings a breadth of global drug development experience including designing studies, operationalizing clinical trials and shaping regulatory strategy, that ultimately led to approval, making him an invaluable asset to the company as we advance our investigational therapies for people living with serious muscle diseases.”
Dr. Bibbiani joins Dyne from Ultragenyx Pharmaceutical Inc., where he served as vice president of global clinical development and oversaw all stages of the development for neuromuscular and neurology product candidates, providing strategic direction and technical leadership to the clinical development team, including for the company’s gene therapy program in DMD. While at Ultragenyx, he was also a member of the DMD Gene Therapy Working Group, comprised of leading experts from the industry and academia collaborating to optimize and provide guidelines for gene therapy in DMD. Previously, Dr. Bibbiani was the vice president of clinical development for PTC Therapeutics, Inc., overseeing multiple clinical trials in DMD and lifecycle management for all products in its neuromuscular portfolio. Prior to PTC Therapeutics he held several roles at Eisai, Inc. as a project and clinical lead, overseeing global clinical development plans and leading multiple New Drug Applications. He received his M.D. and board-certification in neurology from the University of Pisa, Italy. Following that, he completed his fellowship at the National Institutes of Health in Experimental Therapeutics.
“Having spent many years deeply involved in rare muscle disease drug development, I know first hand the urgent need for new therapeutics. Dyne’s FORCE™ platform is an exciting, novel approach leveraging receptor-mediated delivery to target muscle tissue and, ultimately, to potentially modify disease. With robust preclinical data across multiple programs and engagement with community members and other key stakeholders, Dyne is well positioned to execute in the clinic. I look forward to working with the Dyne team, as they are both innovative and passionate about developing therapeutics that have the potential to transform the lives of people with genetically driven muscle diseases,” said Dr. Bibbiani.
About Dyne Therapeutics
Dyne Therapeutics is a clinical-stage muscle disease company focused on advancing innovative life-transforming therapeutics for people living with genetically driven diseases. With its proprietary FORCE™ platform, Dyne is developing modern oligonucleotide therapeutics that are designed to overcome limitations in delivery to muscle tissue seen with other approaches. Dyne has a broad portfolio of programs for serious muscle diseases, including candidates for myotonic dystrophy type 1 (DM1), Duchenne muscular dystrophy (DMD) and facioscapulohumeral muscular dystrophy (FSHD). For more information, please visit https://www.dyne-tx.com/