Key Insights

Highlights

Success Rate

85% trial completion

Published Results

103 trials with published results (24%)

Research Maturity

243 completed trials (57% of total)

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 49/100

Termination Rate

10.3%

44 terminated out of 426 trials

Success Rate

84.7%

-1.8% vs benchmark

Late-Stage Pipeline

12%

52 trials in Phase 3/4

Results Transparency

42%

103 of 243 completed with results

Key Signals

103 with results85% success44 terminated

Data Visualizations

Phase Distribution

301Total
Not Applicable (60)
Early P 1 (8)
P 1 (77)
P 2 (104)
P 3 (41)
P 4 (11)

Trial Status

Completed243
Recruiting47
Unknown45
Terminated44
Active Not Recruiting18
Withdrawn14

Trial Success Rate

84.7%

Benchmark: 86.5%

Based on 243 completed trials

Clinical Trials (426)

Showing 20 of 20 trials
NCT06241560Phase 2RecruitingPrimary

A Study in People With Idiopathic Pulmonary Fibrosis to Test Whether Pirfenidone Influences the Amount of BI 1015550 in the Blood

NCT06485635CompletedPrimary

Real-life-persistence to Antifibrotic Treatments

NCT06238622Phase 3RecruitingPrimary

A Follow-up Study to Test Long-term Treatment With Nerandomilast in People With Pulmonary Fibrosis Who Took Part in a Previous Study With Nerandomilast

NCT06265532Phase 1CompletedPrimary

Collagen-targeted Positron Emission Tomography (PET) Imaging for Assessment of EGCG Effect

NCT07036523Phase 2RecruitingPrimary

A Study to Find Out Whether BI 765423 Has an Effect on Lung Function in People With Idiopathic Pulmonary Fibrosis (IPF) With or Without Standard Treatment

NCT05195918Phase 1CompletedPrimary

Study of Oral Epigallocatechin-3-gallate (EGCG) in IPF Patients

NCT07520110Phase 3Not Yet RecruitingPrimary

Metformin to Attenuate Progressive Respiratory Decline in Idiopathic Pulmonary Fibrosis

NCT06764862Phase 2CompletedPrimary

Evaluating the Efficacy and Safety of of HSK44459 in People With Idiopathic Pulmonary Fibrosis

NCT07036029Phase 1RecruitingPrimary

NAL ER IPF Respiratory Function and Safety Study

NCT07230288Phase 2RecruitingPrimary

Study of ABBV-142 to Assess Adverse Events and Change in Disease Activity in Adult Participants With Idiopathic Pulmonary Fibrosis

NCT05989698Not ApplicableRecruiting

Validation of the C-mo System - Cough Monitoring

NCT07516951Phase 2Not Yet RecruitingPrimary

A Study to Find an Efficacious and Safe Dose of CHF10067 (Zampilimab) in Participants With Idiopathic Pulmonary Fibrosis

NCT04905693Phase 3Enrolling By InvitationPrimary

Extension Study of Inhaled Treprostinil in Subjects With Fibrotic Lung Disease

NCT06967805Phase 2RecruitingPrimary

WISPer: Evaluation of MTX-463 in Participants With Idiopathic Pulmonary Fibrosis (IPF)

NCT06132256Phase 2Active Not RecruitingPrimary

MAXPIRe: Study to Evaluate Axatilimab in Participants With Idiopathic Pulmonary Fibrosis (IPF)

NCT06003426Phase 3Active Not RecruitingPrimary

A Study to Evaluate the Efficacy, Safety, and Tolerability of BMS-986278 in Participants With Idiopathic Pulmonary Fibrosis

NCT04300920Phase 3CompletedPrimary

Prospective Treatment Efficacy in IPF Using Genotype for Nac Selection (PRECISIONS) Trial

NCT06081621Phase 2CompletedPrimary

A Clinical Study to Evaluate the Efficacy and Safety of REGEND001 Cell Therapy on Idiopathic Pulmonary Fibrosis (IPF)

NCT07299695Phase 3RecruitingPrimary

Intravenous Immunoglobulin for the Treatment of Acute Exacerbations of Idiopathic Pulmonary Fibrosis

NCT06317285Phase 2TerminatedPrimary

A Study to Evaluate the Efficacy and Safety of GSK3915393 in Participants With Idiopathic Pulmonary Fibrosis (IPF)

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