Study to Evaluate the Efficacy and Safety of EG-009A Compared to DEX in Patients With COVID-19 Pneumonia
NCT04561180 · Status: WITHDRAWN · Phase: PHASE2 · Type: INTERVENTIONAL
Last updated 2023-07-28
Summary
To study signals of efficacy and safety of a currently available dosage form (IM) of EG-009A in reducing the severity of respiratory disease in patients hospitalized with SARS-CoV-2 virus.
Conditions
Interventions
- DRUG
-
EG-009A
Administered as an Intramuscular injection
- DRUG
-
EG-009A Placebo
Administered as an Intramuscular injection
- DRUG
-
Standard of Care
Standard of Care Treatment for COVID-19 Infection
- DRUG
-
The comparator, Administered as an Intravenous infusion
Sponsors & Collaborators
-
Evergreen Therapeutics, Inc.
lead INDUSTRY
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- QUADRUPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 65 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2022-03-04
- Primary Completion
- 2023-05-01
- Completion
- 2023-05-01
- FDA Drug
- Yes
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