Drug Profile

Research programme: sarcopenia therapeutics - Genflow Biosciences/Revatis

Alternative Names: Muscle progenitor cells therapy

Latest Information Update: 10 Jul 2024

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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 No

30 May 2024 Genflow Biosciences and Revatis agree to co-develop drugs in Sarcopenia
30 May 2024 Early research in Sarcopenia in United Kingdom, Belgium (unspecified route) prior to May 2024

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