Efficacy and Safety of hzVSF-v13 in Patients With COVID-19 Pneumonia

PHASE2CompletedINTERVENTIONAL
Enrollment

115

Participants

Timeline

Start Date

December 11, 2020

Primary Completion Date

August 29, 2021

Study Completion Date

October 28, 2021

Conditions
COVID-19
Interventions
DRUG

hzVSF-v13

Dosage form: 100mg / 200mg of hzVSF-v13 (40 mg/mL in a 5 mL vial) Frequency: Dose at Day 1, 3, 7, D14(if necessary)

DRUG

Placebo (Normal saline solution)

Dosage form: 0.9% NaCl Solution Frequency: Dose at Day 1, 3, 7, D14(if necessary)

Trial Locations (9)

20122

Dipartimento di Medicina Interna, Milan

24127

UOC Pneumologia, Bergamo

197706

"SPb SBIH Municipal Hospital №40", Saint Petersburg

214006

Pokrovskaya Municipal Hospita, Saint Petersburg

Regional Clinical Hospital No1, Smolensk

346918

Central City Hospital of Novoshakhtinsk, Novoshakhtinsk

410053

Regional Clinical Hospital, Saratov

450008

Federal State Budgetary Educational Institution of Higher Education, Ufa

660037

Federal Siberian Scientific and Clinical Center of the Federal Medical and Biological Agency, Krasnoyarsk

Sponsors

Lead Sponsor

All Listed Sponsors
lead

ImmuneMed, Inc.

INDUSTRY

NCT04676971 - Efficacy and Safety of hzVSF-v13 in Patients With COVID-19 Pneumonia | Biotech Hunter | Biotech Hunter