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
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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