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NCT05525182

Efficacy and Safety of ES16001 in Patients With COVID-19

Status unknown Phase 2, PHASE3 Last updated 22 February 2023
What this trial tests

Phase 2, PHASE3 trial testing ES16001 40 mg in COVID-19 in 706 participants. Status unknown.

Timeline
5 July 2021
Primary endpoint
31 December 2023
31 December 2023

Quick facts

Lead sponsorGenencell Co. Ltd.
PhasePhase 2, PHASE3
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingtriple
Primary purposetreatment
Enrollment706
Start date5 July 2021
Primary completion31 December 2023
Estimated completion31 December 2023
Sites3 locations across South Korea

Drugs / interventions tested

Conditions studied

Sponsor

Genencell Co. Ltd. — full company profile →

Who can join

19 and older, any sex, with COVID-19. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is phase II/III, randomized, parallel-group, double-blind, placebo-controlled study. Patients must be at least 19 years of age (or according to the legal age for adult in each country) with confirmed mild or moderate COVID-19 tested positive with a real time reverse transcription polymerase chain reaction (RT-PCR) analysis of rhinopharynx samples. RT-PCR analysis of rhinopharynx samples must be \<4 days old prior to the study enrolment

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for COVID-19

Currently open trials in the same condition.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05525182.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing