A Study to Evaluate the Efficacy and Safety of VB-201 in Patients With COVID-19
NCT04733833 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 5
Last updated 2023-02-01
Summary
The purpose of this Phase 2 study is to test safety, efficacy, and tolerability of an oral preparation of VB-201 in patients with severe COVID-19
Conditions
- Severe COVID-19
Interventions
- DRUG
-
VB-201 + Standard of care
Daily oral administration of VB-201- 160 mg (80 mg BID) with standard of care
- DRUG
-
Standard of care
Standard of care
Sponsors & Collaborators
-
Vascular Biogenics Ltd. operating as VBL Therapeutics
lead INDUSTRY
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 80 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2021-01-26
- Primary Completion
- 2022-10-25
- Completion
- 2022-10-25
Countries
- Israel
Study Locations
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