Clinical trial
A Phase I Study to Determine the Pharmacokinetic Profile, Safety and Tolerability of a Single Dose (50IU/kg) of KW-3357 in Subjects With Congenital Antithrombin Deficiency.
NCT00938288 is registered in ClinicalTrials.gov with Kyowa Kirin Co., Ltd. as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A Phase I Study to Determine the Pharmacokinetic Profile, Safety and Tolerability of a Single Dose (50IU/kg) of KW-3357 in Subjects With Congenital Antithrombin Deficiency.
- Lead sponsor
- Kyowa Kirin Co., Ltd.
- Phase
- Phase 1
- Overall status
- Completed
- Start date
- April 30, 2009
- Completion date
- April 30, 2011
- Enrollment
- 16 (actual)
- Sites
- 8
Conditions
As the registry lists them; a condition with its own page is linked.
congenital antithrombin deficiency