drugset / Trial / NCT07290257

Long-Term Low-Intervention SafEty and Clinical Outcomes Clinical Study of LivmArli® in Patients With Alagille Syndrome or Progressive Familial Intrahepatic Cholestasis in the European Union (LEAP-EU)

NCT07290257

Phase 4 Recruiting 230 enrolled Mirum Pharmaceuticals, Inc.
NaSingle-groupOpen-labelOther

Summary

In patients with Alagille syndrome (ALGS), the key objectives are to evaluate the tolerability, long-term safety (including possible liver toxicity) and long-term efficacy of Livmarli treatment. In patients with Progressive Familial Intrahepatic Cholestasis (PFIC), the key objectives are to evaluate tolerability, long-term safety (including possible liver toxicity and potential impact of chronic exposure to propylene glycol (PG)), long-term efficacy, and growth and development.

Timeline

Start
2025-09-25
Primary completion
2030-09-22
Completion
2030-12-22

Drugs

EvaluationDrugModalityDoseRoute
Subject Maralixibat Small molecule