Key Insights

Highlights

Success Rate

100% trial completion (above average)

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 40/100

Termination Rate

0.0%

0 terminated out of 21 trials

Success Rate

100.0%

+13.5% vs benchmark

Late-Stage Pipeline

19%

4 trials in Phase 3/4

Results Transparency

20%

1 of 5 completed with results

Key Signals

1 with results100% success

Data Visualizations

Phase Distribution

15Total
Not Applicable (2)
Early P 1 (2)
P 1 (3)
P 2 (4)
P 3 (4)

Trial Status

Recruiting12
Completed5
Active Not Recruiting2
Enrolling By Invitation1
Unknown1

Trial Success Rate

100.0%

Benchmark: 86.5%

Based on 5 completed trials

Clinical Trials (21)

Showing 20 of 20 trials
NCT06016842Phase 3RecruitingPrimary

A Long-Term Study of Elafibranor in Adult Participants With Primary Biliary Cholangitis

NCT05896124Phase 2Active Not RecruitingPrimary

CS0159 in Chinese Patients With PBC (Primary Biliary Cholangitis)

NCT07304843Phase 1RecruitingPrimary

A Two-part Study to Investigate the Effects in Adults of Two Doses of Golexanolone in Patients With Primary Biliary Cholangitis (PBC) With Fatigue and Cognitive Dysfunction

NCT07449793RecruitingPrimary

Biochemical Response and Clinical Outcomes in Patients With PBC

NCT06755151Phase 3RecruitingPrimary

Fenofibrate in Primary Biliary Cholangitis: a Real World Study

NCT06755541Phase 3RecruitingPrimary

Fenofibrate in Combination With Ursodeoxycholic Acid in Primary Biliary Cholangitis: a Real World Study

NCT07296458Phase 3RecruitingPrimary

FIREFLY Trial: Fenofibrate Intervention---Randomized Evaluation in First-Line PBC Therapy

NCT06591468Phase 2Enrolling By InvitationPrimary

A Multicenter, Randomized, Controlled Trial of Prednisone Combined With Ursodeoxycholic Acid in the Treatment of Primary Biliary Cholangitis With Moderate to Severe Interface Hepatitis Characteristics

NCT06591455Early Phase 1CompletedPrimary

A Pilot Study of Fenofibrate and Ursodeoxycholic Acid in the Treatment of Newly Diagnosed Primary Biliary Cholangitis

NCT06798454Phase 1CompletedPrimary

Single Ascending Dose Study to Evaluate Safety Tolerability, Pharmacokinetics, and Pharmacodynamics of PVT201 in Healthy Subjects and Patients (PBC/PSC)

NCT07205874RecruitingPrimary

Early Diagnosis of Primary Biliary Cholangitis (PBC) in Patients With Positive Anti-Mitochondrial Antibodies (AMA) and Normal Alkaline Phosphatase (ALP)

NCT07161245Not ApplicableRecruitingPrimary

RELIEF: Multimodal Prehabilitation to Treat Fatigue in Patients With Primary Biliary Cholangitis

NCT07149675RecruitingPrimary

PBC Long-term Outcomes Study

NCT07104201Early Phase 1RecruitingPrimary

Fenofibrate in Subjects With Primary Biliary Cholangitis (PBC)

NCT03188146CompletedPrimary

Performance of Scoring Systems in Chinese Patients With Primary Biliary Cholangitis (PBC) on Ursodeoxycholic Acid

NCT06861465Not ApplicableRecruitingPrimary

EMPower Mechanisms

NCT06767605Recruiting

Spanish Registry of Autoimmune and Cholestatic Liver Diseases (ColHai)

NCT06604923Active Not RecruitingPrimary

PET/CT Scans Using the Tracer 11C-Csar, a Bile Acid Analog, to Depict and Visualize Changes in the Hepatobiliary System in Patients With Primary Biliary Cholangitis Before and After Treatment.

NCT04047160Phase 1CompletedPrimary

Safety, Tolerability of OP-724 in Patients With Primary Biliary Cholangitis (Phase I)

NCT03521297Phase 2UnknownPrimary

Probiotics in PBC Patients of Poor Response to UDCA

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