Intravenous Immunoglobulin (IVIG, Bioven) Efficacy Assess for COVID-19 / SARS-CoV-2 Severe Pneumonia Complex Treatment

PHASE3CompletedINTERVENTIONAL
Enrollment

76

Participants

Timeline

Start Date

May 7, 2020

Primary Completion Date

September 15, 2020

Study Completion Date

September 15, 2020

Conditions
Covid19Pneumonia
Interventions
DRUG

IVIG

Patients in the study group receive the drug Bioven, 10% solution for infusions produced by LLC Biopharma Plasma 0,8-1,0 g/kg once a day for 2 days (total course dose - 1.6-2.0 g/kg) as well as base treatment recommended by the protocol of COVID-19 coronavirus infection treatment depending on the severity of their condition according to the prescription sheet.

Trial Locations (9)

21021

"Site 06 - Vinnytsia City Clinical Hospital №1", Vinnitsia

43000

"Site 09 - Volyn Regional Clinical Hospital", Lutsk

46006

"Site 07 - Ternopil City Municipal Ambulance Hospital", Ternopil

65021

"Site 04 - City Clinical Infectious Diseases Hospital, Odesa", Odesa

76018

"Site 08 - Central City Clinical Hospital of Ivano-Frankivsk City Council", Ivano-Frankivsk

79010

"Site 03 - Lviv Regional Infectious Diseases Clinical Hospital", Lviv

09112

"Site 02 - Bila Tserkva City Hospital №3", Bila Tserkva

03110

"Site 01 - Kyiv City Clinical Hospital №17", Kyiv

"Site 05 - Kyiv City Clinical Hospital №4", Kyiv

Sponsors
All Listed Sponsors
collaborator

Lviv National Medical University

OTHER

collaborator

Vinnitsa National Medical University

OTHER

lead

Biopharma Plasma LLC

INDUSTRY

NCT04500067 - Intravenous Immunoglobulin (IVIG, Bioven) Efficacy Assess for COVID-19 / SARS-CoV-2 Severe Pneumonia Complex Treatment | Biotech Hunter | Biotech Hunter