Project Details
Description
Randomized, multicenter, double-blind, placebo-controlled, parallel-group Phase III study to investigate the efficacy, safety, and tolerability of 2 different doses of IgPro20 (subcutaneous immunoglobulin) for the treatment
Status | Finished |
---|---|
Effective start/end date | 1/1/14 → 4/30/18 |
Funding
- CSL BEHRING GMBH
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