Key Insights

Highlights

Success Rate

100% trial completion (above average)

Clinical Risk Assessment

Based on trial outcomes

Low Risk

Score: 27/100

Termination Rate

0.0%

0 terminated out of 23 trials

Success Rate

100.0%

+13.5% vs benchmark

Late-Stage Pipeline

17%

4 trials in Phase 3/4

Results Transparency

40%

6 of 15 completed with results

Key Signals

6 with results100% success

Data Visualizations

Phase Distribution

14Total
Not Applicable (2)
P 1 (2)
P 2 (6)
P 3 (2)
P 4 (2)

Trial Status

Completed15
Recruiting5
Unknown2
Suspended1

Trial Success Rate

100.0%

Benchmark: 86.5%

Based on 15 completed trials

Clinical Trials (23)

Showing 20 of 20 trials
NCT06850038RecruitingPrimary

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

NCT05035030Phase 3RecruitingPrimary

Long-term Safety and Efficacy of Odevixibat in Patients With Alagille Syndrome

NCT05488067Phase 4CompletedPrimary

Atorvastatin Therapy on Xanthoma in Alagille Syndrome

NCT07290257Phase 4RecruitingPrimary

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

NCT00571272Suspended

Longitudinal Study of Genetic Causes of Intrahepatic Cholestasis (LOGIC)

NCT01793168Recruiting

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

NCT06193928RecruitingPrimary

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

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).

NCT02922751Completed

FibroScan™ in Pediatric Cholestatic Liver Disease (FORCE)

NCT03082937Phase 1Completed

An Open Label, Single-dose, Single Period ADME Study of A4250 in Healthy Subjects

NCT02963077Phase 1Completed

A Safety and Pharmakokinetic Study of A4250 Alone or in Combination With A3384

NCT04674761Phase 3CompletedPrimary

Efficacy and Safety of Odevixibat in Patients With Alagille Syndrome

NCT05846854Not ApplicableUnknownPrimary

Decreasing Hemorrhage Risk in Children With Alagille Syndrome

NCT02047318Phase 2CompletedPrimary

An Extension Study to Evaluate the Long-Term Safety and Durability of Effect of LUM001 in the Treatment of Cholestatic Liver Disease in Subjects With Alagille Syndrome (ALGS)

NCT04530994UnknownPrimary

A Maralixibat Expanded Access Program for Patients With Cholestatic Pruritus Associated With Alagille Syndrome (ALGS)

NCT02160782Phase 2CompletedPrimary

Safety and Efficacy Study of LUM001 (Maralixibat) With a Drug Withdrawal Period in Participants With Alagille Syndrome (ALGS)

NCT02117713Phase 2CompletedPrimary

An Extension Study to Evaluate the Long-Term Safety and Durability of Effect of LUM001 in the Treatment of Cholestatic Liver Disease in Pediatric Subjects With Alagille Syndrome

NCT01903460Phase 2CompletedPrimary

Safety and Efficacy Study of LUM001 in the Treatment of Cholestatic Liver Disease in Patients With Alagille Syndrome

NCT02057692Phase 2CompletedPrimary

Evaluation of LUM001 in the Reduction of Pruritus in Alagille Syndrome

NCT02131623CompletedPrimary

Validation of the Itch Reported Outcome (ItchRO) Diaries in Pediatric Cholestatic Liver Disease

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