Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

Moderate Risk

Score: 45/100

Failure Rate

25.0%

4 terminated/withdrawn out of 16 trials

Success Rate

66.7%

-19.8% vs industry average

Late-Stage Pipeline

38%

6 trials in Phase 3/4

Results Transparency

63%

5 of 8 completed trials have results

Key Signals

2 recruiting5 with results

Enrollment Performance

Analytics

Phase 3
6(40.0%)
Phase 1
5(33.3%)
Phase 2
4(26.7%)
15Total
Phase 3(6)
Phase 1(5)
Phase 2(4)

Activity Timeline

Global Presence

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Clinical Trials (16)

Showing 16 of 16 trials
NCT07191535Phase 2Not Yet Recruiting

Effect of Linvemastat in Patients With Partially Controlled Asthma (syMMPonia)

Role: lead

NCT06475781Phase 2Recruiting

Study to Evaluate Safety and Efficacy of Mirivadelgat in PH-ILD

Role: lead

NCT05493709Phase 3Active Not Recruiting

Efficacy, Safety, and Pharmacokinetics of Leuprolide Mesylate in Subjects With Central Precocious Puberty

Role: lead

NCT06795178Phase 3Withdrawn

Efficacy, Safety, and Pharmacokinetics of FP-014, 11.25 mg in Patients With Advanced Prostate Cancer

Role: lead

NCT06795191Phase 3Withdrawn

Efficacy, Safety, and Pharmacokinetics of FP-014, 22.5 mg in Patients With Advanced Prostate Cancer

Role: lead

NCT04522375Phase 1Withdrawn

A Dose Escalation Study of FP-045 in Patients With Fanconi Anemia

Role: lead

NCT04761393Recruiting

Characterizing Matrix Metalloproteinase-12 (MMP12) in Sputum

Role: collaborator

NCT06334211Phase 1Completed

Safety, Tolerability, and Pharmacokinetics, of Single and Multiple Ascending Doses of FP-020 in Healthy Adult Volunteers

Role: lead

NCT03858686Phase 2Completed

The Effect of FP-025, on Allergen-induced Airway Responses in Mild Eosinophilic House Dust Mite (HDM)-Allergic Asthma.

Role: lead

NCT04750278Phase 2Terminated

A Phase 2/3 Study to Evaluate FP-025 in Patients With Severe to Critical COVID 19

Role: lead

NCT02238834Phase 1Completed

Phase 1 Safety, Tolerability and Pharmacokinetics (PK) Study of FP-025 in Healthy Volunteers

Role: lead

NCT03686930Phase 1Completed

Multiple-Dose, Dose-Escalation Study to Evaluate the Safety/Tolerability and Pharmacokinetics of FP-045

Role: lead

NCT03261999Phase 3Completed

Safety, Efficacy, and Pharmacokinetic Behavior of Leuprolide Mesylate (LMIS 25 mg) in Subjects With Prostate Cancer

Role: lead

NCT02712320Phase 3Completed

Open-Label Safety Extension Study in Patients Who Have Previously Participated and Have Benefited From LMIS 50 mg

Role: lead

NCT02234115Phase 3Completed

Safety, Efficacy, and Pharmacokinetic Behavior of Leuprolide Mesylate in Subjects With Advanced Prostate Carcinoma

Role: lead

NCT03304964Phase 1Completed

A Phase 1, Pharmacokinetics of the MMP-12 Inhibitor FP-025 After Multiple Oral Ascending Doses in Healthy Subjects

Role: lead

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