Efficacy, Safety and Pharmacokinetic of Virchow IVIG in PID Patients

PHASE3Not yet recruitingINTERVENTIONAL
Enrollment

44

Participants

Timeline

Start Date

July 1, 2025

Primary Completion Date

December 1, 2026

Study Completion Date

December 1, 2026

Conditions
Primary Immunodeficiency Diseases (PID)
Interventions
DRUG

IVIG-VImmune

V-Immune will be administered at 200-800 mg/kg dose as a single infusion every 3 or 4 weeks. Patients will be treated with V-Immune from Week 0 (first dose) till Week 48 at an investigator-recommended dose

DRUG

IVIG-Immuglo

Immuglo will be administered at 200-800 mg/kg dose as a single infusion every 3 or 4 weeks. Patients will be treated with V-Immune from Week 0 (first dose) till Week 48 at an investigator-recommended dose

Trial Locations (2)

302013

Jyoti Nursing Home (P) Ltd., Jaipur

441108

All India Institute of Medical Sciences, Nagpur

All Listed Sponsors
lead

Virchow Group

INDUSTRY