Efficacy and Safety of XAV-19 for the Treatment of Moderate-to-severe COVID-19
NCT04928430 · Status: TERMINATED · Phase: PHASE2/PHASE3 · Type: INTERVENTIONAL · Enrollment: 290
Last updated 2023-01-23
Summary
The purpose of this study is to evaluate the efficacy and safety of XAV-19 drug in patients with moderate-to-severe COVID-19.
Conditions
Interventions
- DRUG
-
XAV-19
150 mg of XAV-19 single IV perfusion
- DRUG
-
Single IV infusion
Sponsors & Collaborators
-
Xenothera SAS
lead INDUSTRY
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- TRIPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2021-04-28
- Primary Completion
- 2022-11-28
- Completion
- 2022-11-28
Countries
- Bulgaria
- Greece
- Romania
- Spain
- Turkey (Türkiye)
Study Locations
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