Success Metrics

Clinical Success Rate
98.2%

Based on 56 completed trials

Completion Rate
98%(56/57)
Active Trials
9(10%)
Results Posted
45%(25 trials)
Terminated
1(1%)

Phase Distribution

Ph not_applicable
3
3%
Ph phase_1
15
17%
Ph phase_3
13
15%
Ph phase_4
9
10%
Ph phase_2
36
41%

Phase Distribution

15

Early Stage

36

Mid Stage

22

Late Stage

Phase Distribution76 total trials
Phase 1Safety & dosage
15(19.7%)
Phase 2Efficacy & side effects
36(47.4%)
Phase 3Large-scale testing
13(17.1%)
Phase 4Post-market surveillance
9(11.8%)
N/ANon-phased studies
3(3.9%)

Highest Phase Reached

Phase 4

Trial Status & Enrollment

Completion Rate

96.6%

56 of 58 finished

Non-Completion Rate

3.4%

2 ended early

Currently Active

9

trials recruiting

Total Trials

87

all time

Status Distribution
Active(12)
Completed(56)
Terminated(2)
Other(17)

Detailed Status

Completed56
unknown17
Recruiting7
Not yet recruiting3
Active, not recruiting2
Terminated1

Development Timeline

Analytics

Development Status

Total Trials
87
Active
9
Success Rate
98.2%
Most Advanced
Phase 4

Trials by Phase

Phase 115 (19.7%)
Phase 236 (47.4%)
Phase 313 (17.1%)
Phase 49 (11.8%)
N/A3 (3.9%)

Trials by Status

completed5664%
active_not_recruiting22%
not_yet_recruiting33%
recruiting78%
terminated11%
unknown1720%
withdrawn11%

Recent Activity

Clinical Trials (87)

Showing 20 of 87 trialsScroll for more
NCT03109288Phase 1

Targeting Residual Activity By Precision, Biomarker-Guided Combination Therapies of Multiple Sclerosis (TRAP-MS)

Recruiting
NCT06241560Phase 2

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

Recruiting
NCT05060822Phase 2

Phase ll Study of HEC585 in Patients With IPF

Active Not Recruiting
NCT07082842Phase 3

Confirmatory Clinical Study of HEC585 Tablets in Patients With IPF

Recruiting
NCT06485635

Real-life-persistence to Antifibrotic Treatments

Completed
NCT07454291Phase 1

A Phase 1, Open-Label Study to Evaluate Pharmacokinetics and Drug-drug Interactions of ENV-101 (Taladegib) in Healthy Participants

Not Yet Recruiting
NCT03177291Phase 1

Pirfenidone Combined With Standard First-Line Chemotherapy in Advanced-Stage Lung NSCLC

Completed
NCT06070610Phase 1

A Study in Healthy Men to Test Whether BI 1015550 Influences the Amount of Nintedanib and Pirfenidone in the Blood

Completed
NCT03385668Phase 2

Pilot Study of Pirfenidone in Pulmonary Fibrosis With Anti-myeloperoxydase Antibodies

Completed
NCT06928272Phase 3

Long Covid (LC)-REVITALIZE - A Long Covid Repurposed Drug Study

Recruiting
NCT05321420Phase 2

LYT-100 in Patients With Idiopathic Pulmonary Fibrosis (IPF)

Active Not Recruiting
NCT06253117Phase 2

Evaluation of Pirfenidone as a Novel Therapeutic Strategy Against Recurrent Acute Pancreatitis.

Recruiting
NCT07015398Phase 1

A Study of the Pharmacokinetic Interaction Between Pirfenidone, Nintedanib, and Nalbuphine Extended Release (NAL ER) in Healthy Participants

Completed
NCT05075161Phase 3

Pirfenidone to Prevent Fibrosis in Ards.

Recruiting
NCT05779007

Dose Reduction and Discontinuation With Anti-Fibrotic Medications

Completed
NCT03047031

Post Marketing Surveillance of Nintedanib in Indian Patients With Idiopathic Pulmonary Fibrosis

Completed
NCT03902509Phase 2

A Study About Safety and Efficacy of Pirfenidone to Treat Grade 2 or Grade3 Radiation-induced Lung Injury.

Completed
NCT06224790Phase 4

Perfenidone in Type 2 Diabetic Patients With Diabetic Neuropathy

Completed
NCT05676112

Safety of Nintedanib in Real World in China

Withdrawn
NCT04971746Phase 1

Drug-drug Interaction Study with GLPG4716 and Nintedanib and Pirfenidone in Healthy Subjects

Completed

Drug Details

Intervention Type
DRUG
Total Trials
87