Bioverativ and Sangamo Announce FDA Acceptance of IND Application for Gene-Edited Cell Therapy BIVV003 to Treat Sickle Cell Disease
Sangamo Therapeutics, Inc. (SGMO)
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Source: Business Wire
WALTHAM, Mass. & RICHMOND, Calif.--(BUSINESS WIRE)-- Bioverativ Inc., a Sanofi company dedicated to transforming the lives of people with rare blood disorders, and Sangamo Therapeutics, Inc. (NASDAQ:SGMO) announced today that the U.S. Food and Drug Administration (FDA) has accepted the Investigational New Drug (IND) application for BIVV003, a gene-edited cell therapy candidate for the treatment of people with sickle cell disease. Bioverativ and Sangamo are developing BIVV003 as part of an exclusive worldwide collaboration to develop and commercialize gene-edited cell therapies for sickle cell disease and beta thalassemia. This press release features multimedia. View the full release here:https://www.businesswire.com/news/home/20180516005404/en/ “This acceptance marks the second IND for this gene-editing approach in less than a year, and the first for a gene-edited therapy in sickle cell disease,” said Ken Huttner,
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SGMO
Earnings
- 3/13/24 - Miss
SGMO
Sec Filings
- 4/19/24 - Form ARS
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- 4/5/24 - Form SC
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