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Clinical studies
Vonafexor is currently in Phase 2 clinical studies
- Phase 2 in CKD and suspected MASH: Vonafexor in patients with impaired renal function and suspected Metabolic Dysfunction-associated Steatohepatitis (MASH) Learn more about the clinical study
- Phase 2 ALPESTRIA-1 in Alport syndrome: Vonafexor Fixed Dose-escalation Safety and Proof-of-concept Study in Patients With at Risk of Progression Alport Syndrome. Learn more about ALPESTRIA-1 study
Vonafexor is already supported by 9 clinical studies
- Phase 2a LIVIFY study: Safety,
Pipeline
ENYO Pharma is advancing its pipeline with Vonafexor series for diseases with impaired kidney function as CKD, Alport syndrome, NASH and DKD.
Vonafexor series
ENYO Pharma is advancing its pipeline with Vonafexor series for diseases with impaired kidney function like Alport syndrome, CKD and MASH*.
Vonafexor (EYP001)
Vonafexor is a synthetic non-steroidal, non-bile acid farnesoid X receptor (FXR)** agonist. It activates FXR with a high selectivity compared to other nuclear receptors and does not display any activity on bile acid receptor TGR5.
This small molecule has a different structure compared to other FXR agonists and induces a differential set of target genes based on ligand binding patterns.
5th CKD Summit – Chronic Kidney Disease Drug Development
7-9 March, 2023
Boston, MA
ENYO was attending the 5th Chronic Kidney Disease Drug Development Summit, an industry forum sharing cross-industry insight to bring effective therapies to patients suffering from kidney diseases expanding also to rare renal disorders.