drugset / Trial / NCT00814320

Gammagard Liquid and rHuPH20 in PID

NCT00814320 ↗

Phase 3 Completed 89 enrolled Baxalta now part of Shire
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of the study is to develop a subcutaneous treatment option for participants with Primary Immunodeficiency Diseases (PID) that allows an administration of Immune Globulin Intravenous (Human), 10% at the same frequency as IV administration.

Timeline

Start
2008-12-18
Primary completion
2010-11-11
Completion
2010-11-11

Outcome

Results reported · no primary-endpoint met/missed verdict (typical of a dose-finding / safety study)

registry p <0.0001; Poisson 0.025; Poisson; note: Testing the null hypothesis of 1 VASBI/year against a one-sided alternative at the 0.01 level of statistical significance. NCT00814320 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Immune Globulin Intravenous (Human) Protein / enzyme biologic — Intravenous
Subject recombinant human hyaluronidase Protein / enzyme biologic — Subcutaneous