drugset / Trial / NCT02247141

A Multi-centre Open Study to Assess the Safety and Efficacy of Subgam®

NCT02247141 ↗

Phase 3 Completed Bio Products Laboratory

Summary

The primary objective was to determine the efficacy of Human Normal Immunoglobulin (Subgam®) given subcutaneously by weekly infusion to patients with primary antibody deficiency. The secondary objective was to determine the safety of Subgam® given subcutaneously by weekly infusion to patients with primary antibody deficiency.

Timeline

Start
2000-06
Primary completion
2005-01
Completion
—

Drugs

EvaluationDrugModalityDoseRoute
Subject Subgam Protein / enzyme biologic — Subcutaneous

Indications