Drug Profile

Research programme: fibrotic disease therapeutics - Bristol-Myers Squibb/Harvard Stem Cell Institute

Latest Information Update: 28 May 2022

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At a glance

Orphan Drug Status

Orphan designation is assigned by a regulatory body to encourage companies to develop drugs for rare diseases.

No
New Molecular Entity Yes

28 May 2022 No recent reports of development identified for research development in Fibrosis in USA
12 Apr 2018 Bristol-Myers Squibb establishes collaboration with Harvard Stem Cell Institute for the development of anti-fibrotic drugs
12 Apr 2018 Early research in Fibrosis in USA (unspecified route)

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