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

No results posted yet for this study

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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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 NCT04733833 on ClinicalTrials.gov