Follow-up Study of Subcutaneous Immune Globulin in Patients Requiring IgG Replacement Therapy (Japan Study)

Registry ID
EUCTR2014-003609-14
Source registry
EUCTR
Phase
PHASE3
Sponsor
CSL Behring
Last update
2026-08-16

Conditions

Summary

To assess the long-term safety, tolerability, and efficacy of IgPro20 in subjects with primary immunodeficiency (PID) as a follow-up to the pivotal study ZLB06_002CR (NCT01199705).

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