Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

Low Risk

Score: 30/100

Failure Rate

10.0%

4 terminated/withdrawn out of 40 trials

Success Rate

84.0%

-2.5% vs industry average

Late-Stage Pipeline

28%

11 trials in Phase 3/4

Results Transparency

86%

18 of 21 completed trials have results

Key Signals

8 recruiting18 with results

Enrollment Performance

Analytics

Phase 2
20(58.8%)
Phase 3
10(29.4%)
Phase 1
3(8.8%)
Phase 4
1(2.9%)
34Total
Phase 2(20)
Phase 3(10)
Phase 1(3)
Phase 4(1)

Activity Timeline

Global Presence

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Clinical Trials (40)

Showing 20 of 40 trials
NCT05050136Phase 2Recruiting

A Study to Evaluate Efficacy and Safety of an Investigational Drug Named Volixibat in Patients With Itching Caused by Primary Biliary Cholangitis

Role: lead

NCT07411716Recruiting

Pediatric Evaluation and Registry for Liver Cholestasis in Canada

Role: collaborator

NCT07454837Phase 2Recruiting

Study to Evaluate Switching to Brelovitug for the Treatment of CHD in Participants Receiving Bulevirtide

Role: lead

NCT07209462Phase 2Recruiting

Study of MRM-3379 in Male Participants With Fragile X Syndrome (BLOOM)

Role: lead

NCT06553768Phase 3Active Not Recruiting

Evaluation of Maralixibat in Pruritus Associated With General Cholestatic Liver Disease (EXPAND)

Role: lead

NCT07200908Phase 3Recruiting

A Trial Evaluating Brelovitug (BJT-778) vs Bulevirtide for the Treatment of Chronic Hepatitis Delta Infection (AZURE-2)

Role: lead

NCT07298330Phase 3Recruiting

A Trial Evaluating Brelovitug vs Delayed Treatment for the Treatment of Chronic Hepatitis Delta Infection (AZURE-4)

Role: lead

NCT06907290Phase 2Active Not Recruiting

A Trial Evaluating BJT-778 vs Delayed Treatment for the Treatment of Chronic Hepatitis Delta Infection

Role: lead

NCT07389031Phase 2Not Yet Recruiting

Maralixibat for Intrahepatic Cholestasis of Pregnancy

Role: collaborator

NCT04663308Phase 2Active Not Recruiting

A Study to Evaluate Efficacy and Safety of an Investigational Drug Named Volixibat in Patients With Itching Caused by Primary Sclerosing Cholangitis (PSC)

Role: lead

NCT07290257Phase 4Recruiting

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

Role: lead

NCT04168385Phase 2Completed

MRX-800: A Long-Term Safety Study of Maralixibat in the Treatment of Cholestatic Liver Disease in Subjects Who Previously Participated in a Maralixibat Study

Role: lead

NCT05368038Enrolling By Invitation

ScreenPlus: A Comprehensive, Flexible, Multi-disorder Newborn Screening Program

Role: collaborator

NCT04185363Phase 3Completed

An Extension Study of Maralixibat in Patients With Progressive Familial Intrahepatic Cholestasis (PFIC)

Role: lead

NCT06193928Recruiting

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

Role: lead

NCT04524390Phase 2Completed

Evaluation of Maralixibat in Biliary Atresia Response Post-Kasai

Role: lead

NCT04729751Phase 2Completed

A Study to Evaluate the Safety and Tolerability of Maralixibat in Infant Participants With Cholestatic Liver Diseases Including Progressive Familial Intrahepatic Cholestasis (PFIC) and Alagille Syndrome (ALGS).

Role: lead

NCT04270682Phase 3Completed

Study to Evaluate Patients With Cerebrotendinous Xanthomatosis (RESTORE)

Role: lead

NCT04718961Phase 2Terminated

A Placebo-controlled Study of Volixibat in Subjects With Elevated Serum Bile Acids Associated With Intrahepatic Cholestasis of Pregnancy (OHANA)

Role: lead

NCT03905330Phase 3Completed

A Study to Evaluate the Efficacy and Safety of Maralixibat in Subjects With Progressive Familial Intrahepatic Cholestasis (MARCH-PFIC)

Role: lead