– USA, NC – BioCryst Pharmaceuticals, Inc. (Nasdaq: BCRX) today announced that the company has appointed clinical rare disease expert, Helen Thackray, M.D., FAAP, to its board of directors.
“As a physician and chief medical officer, Helen adds important, complementary and contemporary clinical rare disease experience to our board as BioCryst prepares to launch oral BCX7353 to patients next year, and advances our multiple clinical rare disease programs,” said Robert Ingram, chairman of BioCryst.
About Dr Helen Thackray
Dr. Thackray currently serves as the chief medical officer and senior vice president of clinical development at GlycoMimetics, Inc., a clinical-stage biotechnology company advancing a novel pipeline of orphan drug candidates to address unmet needs for patients.
She joined GlycoMimetics in 2006 and leads their orphan product, fast track, and breakthrough therapy programs at all stages of development in rare diseases. Prior to joining GlycoMimetics, Dr. Thackray was vice president of clinical development at Biosynexus, and served for over a decade on the research ethics review board of the National Center for Healthcare Statistics, part of the Centers for Disease Control and Prevention.
She is a board-certified pediatrician, practicing and serving on the faculty of the Children’s National Medical Center and George Washington University School of Medicine and Health Sciences from 2000-2019. Dr. Thackray has authored more than 60 peer-reviewed articles and presentations.
“Advocacy for patients, and for better therapeutic options for those with rare diseases, has been my central focus throughout my career. With a deep pipeline of home-grown oral medicines for rare diseases, BioCryst is positioned to deliver dramatic improvements for patient care. I am excited to join BioCryst as the company makes the transition from clinical to commercial with its first rare disease program,” Dr. Thackray said.
Dr. Thackray holds a Bachelor of Science degree in biological sciences from Stanford University, and an M.D. from the George Washington University School of Medicine and Health Sciences. She completed her pediatric residency and chief residency at Children’s National Medical Center, trained in medical genetics at the National Human Genome Research Institute at the National Institutes of Health, and is a Fellow of the American Academy of Pediatrics.
About BioCryst Pharmaceuticals
BioCryst discovers novel, oral small-molecule medicines that treat rare diseases in which significant unmet medical needs exist and an enzyme plays a key role in the biological pathway of the disease. BioCryst has several ongoing development programs including BCX7353, an oral treatment for hereditary angioedema; BCX9930, an oral Factor D inhibitor for the treatment of complement-mediated diseases; galidesivir, a potential treatment for Marburg virus disease and Yellow Fever, and a preclinical program to develop oral ALK-2 inhibitors for the treatment of fibrodysplasia ossificans progressiva. RAPIVAB, a viral neuraminidase inhibitor for the treatment of influenza, is BioCryst’s first approved product and has received regulatory approval in the U.S., Canada, Australia, Japan, Taiwan, Korea and the European Union. Post-marketing commitments for RAPIVAB are ongoing.
For more information: https://www.biocryst.com
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