drugset / Trial / NCT02093923
A Double-Blind, Multiple Ascending Dose Study to Assess Safety, Tolerability and Pharmacokinetics of DX-2930 in Hereditary Angioedema Participants
RandomizedParallel-groupQuadruple-blindTreatment
Summary
The purpose of this study is to evaluate the safety, tolerability, and pharmacokinetics (PK) profile of multiple subcutaneous administrations of DX-2930 across a range of doses in HAE participants.
Timeline
- Start
- 2014-05-14
- Primary completion
- 2015-05-18
- Completion
- 2015-05-18
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Lanadelumab | Monoclonal antibody | 30 mg | Subcutaneous |
| Subject | Lanadelumab | Monoclonal antibody | 100 mg | Subcutaneous |
| Subject | Lanadelumab | Monoclonal antibody | 300 mg | Subcutaneous |
| Subject | Lanadelumab | Monoclonal antibody | 400 mg | Subcutaneous |