Zydus MASH trial finds primary endpoint met with 26.5% benefit
Saroglitazar Mg in the phase 2(b) EVIDENCES-X trial met the primary endpoint by resolving steatohepatitis without worsening fibrosis in MASH. The treatment difference was 26.5% with 189 participants treated for 52 weeks. The result represents a meaningful step in Zydus’s MASH programme, building on DCGI approval of saroglitazar for MASH and MASLD in India in 2020.