CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 168 enrolled
Drug / intervention
NP-120 (Ifenprodil)drug
Likely dose
NP-120 (Ifenprodil) 20 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

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

Search/NCT04382924
NCT04382924Phase 3Completed

A Randomized Open Label Phase 2b/3 Study of the Safety and Efficacy of NP-120 (Ifenprodil) for the Treatment of Hospitalized Patient With Confirmed COVID-19 Disease

Algernon Pharmaceuticals·interventional·Posted May 11, 2020·Updated Dec 3, 2021

In Brief

A Phase 3 clinical trial evaluating NP-120 (Ifenprodil) for COVID. Completed, enrolled 168 participants across 10 sites in 4 countries.

Detailed Summary

The purpose of this adaptive trial is to determine the clinical efficacy of Ifenprodil in the treatment of patients infected with COVID-19. This Protocol is largely based on the recommendations of the World Health Organization (WHO) R\&D Blueprint Clinical Trials Expert Group COVID-19 Therapeutic Trial Synopsis, and associated Master Protocol. The choice of the primary outcome measure will be determined by a pilot study of the first 150 subjects. Subject clinical status (on a 7-point ordinal scale) at day 15 in treatment versus the control group is the default primary endpoint.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsCOVID
CountriesAustralia, Philippines, Romania, United States

Timeline

Phase 3CompletedFinished
202120222023202420252026
First PostedMay 11, 2020
Enrollment StartAug 5, 2020
Primary CompletionDec 24, 2020
Study CompletionJan 26, 2021
TodayJul 2, 2026
Enrollment to primary: 5 monthsPosted 6.1 years ago

Interventions

NP-120 (Ifenprodil)drug

Ifenprodil, 20 mg TID Ifenprodil, 40 mg TID