Efficacy and Safety of DWJ1248 With Remdesivir in Severe COVID-19 Patients

NCT04713176 · Status: TERMINATED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 240

Last updated 2023-09-29

No results posted yet for this study

Summary

Efficacy and Safety of DWJ1248 with Remdesivir in Severe COVID-19 Patients

Conditions

  • Severe COVID-19

Interventions

DRUG

DWJ1248 with Remdesivir

1 tablet of DWJ1248 TID(up to 14 days) PO, Remdesivir(up to 5 or 10 days) IV

DRUG

Placebo with Remdesivir

1 tablet of placebo TID(up to 14 days) PO, Remdesivir(up to 5 or 10 days) IV

Sponsors & Collaborators

  • Daewoong Pharmaceutical Co. LTD.

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
19 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-02-02
Primary Completion
2022-05-02
Completion
2022-12-09

Countries

  • South Korea

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04713176 on ClinicalTrials.gov