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Clinical Trial Summary

The objectives of the study are to: 1. Evaluate the safety and tolerability of subcutaneously administered CINRYZE with recombinant human hyaluronidase (rHuPH20) in subjects with hereditary angioedema (HAE) who previously participated in CINRYZE Study 0624-200 (NCT01095497) 2. Characterize the pharmacokinetics and pharmacodynamics of subcutaneously administered CINRYZE with rHuPH20 3. Assess the immunogenicity of CINRYZE following subcutaneous (SC) administration of CINRYZE with rHuPH20


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01426763
Study type Interventional
Source Takeda
Contact
Status Completed
Phase Phase 2
Start date September 12, 2011
Completion date November 28, 2011

See also
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