Key Insights

Highlights

Success Rate

89% trial completion (above average)

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 50/100

Termination Rate

5.4%

2 terminated out of 37 trials

Success Rate

88.9%

+2.3% vs benchmark

Late-Stage Pipeline

3%

1 trials in Phase 3/4

Results Transparency

13%

2 of 16 completed with results

Key Signals

2 with results89% success

Data Visualizations

Phase Distribution

21Total
Not Applicable (4)
P 1 (8)
P 2 (8)
P 3 (1)

Trial Status

Completed16
Recruiting7
Active Not Recruiting5
Not Yet Recruiting3
Unknown3
Terminated2

Trial Success Rate

88.9%

Benchmark: 86.6%

Based on 16 completed trials

Clinical Trials (37)

Showing 20 of 20 trials
NCT05147597CompletedPrimary

Turkish Validity and Reliability of SGRQ-I

NCT07790614RecruitingPrimary

Photon-counting CT Scan vs Standard HRCT Scan in the Identification of Idiopathic Pulmonary Fibrosis

NCT06181370Phase 1CompletedPrimary

Phase I Study to Assess Safety, Tolerability, PK and PD of AGMB-447 in Healthy Participants and Participants With IPF

NCT06644144Recruiting

P4O2 ILD Extension

NCT07528703Phase 1Not Yet RecruitingPrimary

A Clinical Study to Evaluate the Safety, Tolerability and Pharmacokinetic Characteristics of RC010 Inhalation Powder in Healthy Participants

NCT07519070Phase 3Not Yet RecruitingPrimary

A Multicenter, Randomized, Double-Blind, Placebo-Controlled Phase III Study to Evaluate the Efficacy and Safety of HSK44459 Tablets in Patients With Idiopathic Pulmonary Fibrosis

NCT07493031Phase 1Not Yet RecruitingPrimary

A PhaseⅠ Study of HW252001 in Healthy Subjects

NCT07448194Phase 1Recruiting

A Phase Ia Clinical Trial of HW241045

NCT06714188CompletedPrimary

Application of Personalized Palliative Care in Patients With Newly Diagnosed Idiopathic Pulmonary Fibrosis

NCT02503657Phase 2Completed

Safety, Tolerability, and Efficacy of MN-001 (Tipelukast) in Patients With Idiopathic Pulmonary Fibrosis

NCT06714812Active Not RecruitingPrimary

Diarrheal Adverse Events in Caucasian Patients With Idiopathic Pulmonary Fibrosis Undergoing Treatment With Nintedanib

NCT05895565Phase 1CompletedPrimary

A Multiple Ascending Doses (MAD) Study of PMG1015 in Idiopathic Pulmonary Fibrosis Subjects

NCT05190211Not ApplicableRecruitingPrimary

Telerehabilitation in Patients With Idiopathic Pulmonary Fibrosis

NCT06747923Phase 2RecruitingPrimary

SB17170 Phase 2 Trial in IPF Patients

NCT06331624Phase 2Completed

Biomarker Modulation and the Inhibition of NKT1 Cells by Oral GRI-0621 in Patients With IPF

NCT06310746Phase 1CompletedPrimary

A Randomized, Double-Blind, Placebo-Controlled, Single-Dose Escalation Phase I Clinical Study to Assess the Safety, Pharmacokinetics, and Immunogenicity of HLX6018 in Healthy Subjects

NCT07169253CompletedPrimary

Prognostic Score Comparison in IPF and HP

NCT07139925Active Not RecruitingPrimary

Assessment of Self-Care in Patients With Idiopathic Pulmonary Fibrosis (IPF)

NCT07031362Not ApplicableCompletedPrimary

The Effectiveness of Pulmonary Rehabilitation on Saturation in Patients With Idiopathic Pulmonary Fibrosis

NCT05983471Phase 2Active Not Recruiting

Efficacy and Safety of ME-015 (Suplatast Tosilate) in Cough Related to Idiopathic Pulmonary Fibrosis (COSMIC-IPF)

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