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

No results posted yet for this study

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

Placebo

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

More Related Trials

Entities

Drugs
Diseases

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 NCT04928430 on ClinicalTrials.gov