CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 231 enrolled
Drug / intervention
EDP-235 +1 moredrug
Likely dose
Not stated in record
Key inclusion· 2
  • Confirmed SARS-CoV-2 infection by positive test within 24 hours before randomization
  • COVID-19 symptom onset within 5 days prior to randomization with at least 2 signs/symptoms present, one of at least moderate severity
Key exclusion· 14
  • Prior SARS-CoV-2 infection or any COVID-19 vaccine dose within 90 days before enrollment
  • One or more conditions associated with high risk for severe COVID-19
  • History of hospitalization for medical treatment of COVID-19
  • Currently hospitalized or anticipated need for hospitalization

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT05616728
NCT05616728Phase 2Completed

A Phase 2, Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study to Evaluate the Effects of EDP-235 in Non-hospitalized Adults With Mild or Moderate COVID-19

Enanta Pharmaceuticals, Inc·interventional·Posted Nov 15, 2022·Updated Aug 19, 2024

In Brief

A Phase 2 clinical trial evaluating EDP-235 and Placebo for COVID-19. Completed, enrolled 231 participants across 23 sites in 2 countries.

Detailed Summary

Study of EDP-235 in Non-hospitalized Adults with Mild or Moderate COVID-19.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsCOVID-19
CountriesRomania, United States
Collaborators--

Timeline

Phase 2CompletedFinished
2023202420252026
First PostedNov 15, 2022
Enrollment StartNov 10, 2022
Primary CompletionFeb 8, 2023
Study CompletionJun 29, 2023
TodayJul 2, 2026
Enrollment to primary: 3 monthsPosted 3.6 years ago

Interventions

EDP-235drug

capsule

Placebodrug

capsule