Alagille Syndrome

5

Review clinical trials related to Alagille Syndrome. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

A Study to Observe the Long-term Safety of Odevixibat in Patients With Alagille Syndrome (ALGS) Who Are Receiving Ongoing Treatment

This study will collect information from patients with ALGS who are using odevixibat in their daily lives. Odevixibat is a medication that helps patients with ALGS, a rare disease that affects the liver and causes itching. The main aim of this study is to observe the long-term, everyday safety of the drug odevixibat in patients with ALGS who are receiving ongoing treatment.

Participants needed: 30
Trial details
Age: 6+Biological sex: AllType: ObservationalSponsor: IpsenUpdated: Jul 2, 2026Duration: 2 Years
Eligibility criteria

Diagnosed with ALGS. [+2]

Currently participating in a clinical trial with odevixibat. [+2]

Status: Recruiting

A Study Observing the Long-term, Effectiveness and Safety of Odevixibat (Bylvay) in Patients With Alagille Syndrome (ALGS) Who Are Receiving Ongoing Treatment

This study will collect information from patients with Alagille syndrome (ALGS) as they use odevixibat (Bylvay) in their daily lives. Odevixibat is a medicine that helps patients with ALGS, a rare disease that harms their liver and causes itching. The main aim of this study is to observe the long-term, everyday effectiveness and safety of the drug odevixibat in patients with ALGS who are receiving ongoing treatment.

Participants needed: 30
Trial details
Biological sex: AllType: ObservationalSponsor: IpsenUpdated: Jul 2, 2026Locations: 10Duration: 2 Years
Eligibility criteria

Diagnosed with ALGS. [+2]

Currently participating in a clinical trial with odevixibat. [+3]

Status: Recruiting

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)

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.

Participants needed: 230
Trial details
Phase: Phase 4Age: 2+Biological sex: AllType: InterventionalSponsor: Mirum Pharmaceuticals, Inc.Updated: Jun 23, 2026Locations: 15
Eligibility criteria

Understand and execute an Informed consent and assent (as applicable) [+6]

History of Liver Transplant [+5]

Status: Recruiting

Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford

CoRDS, or the Coordination of Rare Diseases at Sanford, is based at Sanford Research in Sioux Falls, South Dakota. It provides researchers with a centralized, international patient registry for all rare diseases. This program allows patients and researchers to connect as easily as possible to help advance treatments and cures for rare diseases. The CoRDS team works with patient advocacy groups, individuals and researchers to help in the advancement of research in over 7,000 rare diseases. The registry is free for patients to enroll and researchers to access. Visit sanfordresearch.org/CoRDS to enroll.

Participants needed: 20,000
Trial details
Biological sex: AllType: ObservationalSponsor: Sanford HealthUpdated: May 29, 2025Locations: 2Duration: 100 Years
Eligibility criteria

Diagnosis of a rare disease, a disease of unknown prevalence, undiagnosed or an...

Diagnosis of a disease which is not rare

Status: Recruiting

Long-Term SafEty and Clinical Outcomes of LivmArli in Patients in the United States (LEAP-US)

The objective of this 5-year, prospective, observational cohort study is to evaluate the long-term safety and clinical outcomes of patients with Alagille syndrome (ALGS) or Progressive familial intrahepatic cholestasis (PFIC) treated with Livmarli.

Participants needed: 70
Trial details
Biological sex: AllType: ObservationalSponsor: Mirum Pharmaceuticals, Inc.Updated: May 25, 2025Locations: 8Duration: 5 Years
Eligibility criteria

A clinically and/or genetically confirmed ALGS diagnosis or PFIC diagnosis [+1]

Refusal to provide informed consent/assent (if required by the local IRB) [+4]