drugset / Trial / NCT00242385
Pharmacokinetic Study of ARALAST (Human Alpha1- PI)
Phase 1
Completed
25 enrolled
Baxalta now part of Shire
Baxter Healthcare, Ltd. (New Zealand), Baxter Healthcare Pty. Ltd. (Australia) · collab
RandomizedCrossoverDouble-blindTreatment
Summary
The primary purpose of this study is to characterize the pharmacokinetic profile of intravenous Aralast Fraction (Fr.) IV-1, a sterile, stable, lyophilized preparation of functionally intact human Alpha1- Proteinase Inhibitor (α1-PI). This pharmacokinetic study will be a randomized controlled clinical trial with a cross-over design. Twenty-four subjects will be enrolled into the study. Overall study duration will be approximately 6-8 months.
Timeline
- Start
- 2005-12-20
- Primary completion
- 2006-06-05
- Completion
- 2006-06-05
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Alpha 1-Antitrypsin | Protein / enzyme biologic | 60 mg/kg | Intravenous |