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A Single Increasing Dose Study to Assess Safety and Tolerability of DX-2930 in Healthy Subjects

Hereditary Angioedema (HAE) Clinical Trial

Official title:
A Phase 1, Double-Blind, Single Ascending Dose Study to Assess Safety, Tolerability and Pharmacokinetics of DX-2930 (Recombinant Fully Human Antibody Inhibitor of Plasma Kallikrein) in Healthy Subjects

Clinical Trial Summary

The purpose of this study is to assess the safety and tolerability of the study drug (DX-2930) administered subcutaneously in healthy subjects. Subjects will be randomized to receive DX-2930 or placebo.

Clinical Trial Description

Approximately 32 healthy subjects will be randomized to receive DX-2930 or placebo. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01923207
Study type Interventional
Source Takeda
Contact
Status Completed
Phase Phase 1
Start date August 12, 2013
Completion date January 7, 2014
View Details
See also
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