Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

Moderate Risk

Score: 45/100

Failure Rate

8.9%

4 terminated/withdrawn out of 45 trials

Success Rate

90.5%

+4.0% vs industry average

Late-Stage Pipeline

0%

0 trials in Phase 3/4

Results Transparency

24%

9 of 38 completed trials have results

Key Signals

1 recruiting9 with results

Enrollment Performance

Analytics

Phase 1
33(73.3%)
Phase 2
12(26.7%)
45Total
Phase 1(33)
Phase 2(12)

Activity Timeline

Global Presence

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Clinical Trials (45)

Showing 20 of 45 trials
NCT07540910Phase 1Recruiting

A Study to Investigate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Single and Multiple Doses of EDP-978 in Healthy Adults

Role: lead

NCT07482657Phase 2Not Yet Recruiting

A Phase 2 Study to Investigate the Efficacy and Safety of Zelicapavir in Participants Aged ≥28 Days to ≤36 Months of Age Infected With Respiratory Syncytial Virus

Role: lead

NCT06170242Phase 2Completed

A Controlled Phase 2a Study to Evaluate the Efficacy of EDP-323 Against Respiratory Syncytial Virus Infection in a Virus Challenge Model

Role: lead

NCT04816721Phase 2Completed

A Study to Evaluate EDP 938 Regimens in Children With RSV

Role: lead

NCT06601192Phase 1Completed

A Study to Investigate the Effects of Zelicapavir (EDP-938) on QTc Interval in Healthy Adults

Role: lead

NCT06917508Phase 1Completed

A Study to Evaluate the Drug-Drug Interaction of EDP-323 With Midazolam, Caffeine, and Rosuvastatin in Healthy Participants

Role: lead

NCT06847464Phase 1Completed

A Drug-Drug Interaction Study to Evaluate the Effects of Itraconazole, Carbamazepine, Quinidine and Fluconazole on the Pharmacokinetics and Safety of EDP-323.

Role: lead

NCT05568706Phase 2Completed

A Study of EDP-938 in Non-hospitalized Adults With RSV Who Are at High Risk for Complications.

Role: lead

NCT04633187Phase 2Terminated

Effects of EDP-938 in Hematopoietic Cell Transplant Recipients Infected With Respiratory Syncytial Virus of the Upper Respiratory Tract

Role: lead

NCT05616728Phase 2Completed

A Study to Evaluate EDP-235 in Non-hospitalized Adults With COVID-19

Role: lead

NCT04196101Phase 2Completed

A Study to Assess EDP-938 for the Treatment of Acute Upper Respiratory Tract Infection With Respiratory Syncytial Virus in Adult Subjects

Role: lead

NCT05587478Phase 1Completed

A Study of EDP-323 in Healthy Subjects

Role: lead

NCT04378010Phase 2Terminated

A Randomized, Double-blind Study to Assess the Safety and Efficacy of EDP-305 in Subjects With Liver-biopsy Proven NASH

Role: lead

NCT05594615Phase 1Completed

Drug-Drug Interaction Study Between EDP-235, Midazolam, Caffeine and Rosuvastatin in Healthy Subjects

Role: lead

NCT05594602Phase 1Completed

Drug-Drug Interaction Study Between EDP-235, Itraconazole, Carbamazepine and Quinidine in Healthy Subjects.

Role: lead

NCT05246878Phase 1Completed

A Study of EDP-235 in Healthy Subjects

Role: lead

NCT03691623Phase 2Completed

A Phase 2a Study to Evaluate EDP-938 in the Virus Challenge Model

Role: lead

NCT04927793Phase 1Completed

Absorption, Metabolism, and Excretion (AME) Study of [14C]EDP-938 in Healthy Male Subjects

Role: lead

NCT04971512Phase 1Terminated

A 2 PART STUDY EVALUATING EDP-721 IN HEALTHY SUBJECTS AND EDP-721 IN COMBINATION WITH EDP-514 IN PATIENTS WITH CHRONIC HEPATITIS B VIRUS INFECTION.

Role: lead

NCT04008004Phase 1Completed

A Study of EDP-514 in Healthy Subjects (Part 1) and Patients With Chronic Hepatitis B Virus Infection (Part 2)

Role: lead