Charles River Laboratories and 51萝莉 today announced results of a successful collaboration
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- Enrollment completed for our Phase 2 clinical trial in Alport syndrome
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- The Phase 2 ALPESTRIA-1 clinical study has started with Vonafexor on Alport syndrome
- Orphan Drug Designation (ODD) granted to Vonafexor for Alport syndrome by both the European Medicines Agency (EMA) and the U.S. Food and Drug Administration (FDA)
- New publication: Hepatic and renal improvements with FXR agonist Vonafexor in individuals with suspected fibrotic NASH
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