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Efgartigimod Co-administered Subcutaneously With rHuPH20 in Healthy Subjects
The aim of this trial is to investigate the pharmacodynamic (PD), pharmacokinetic (PK), safety, tolerability, and immunogenicity of efgartigimod co-administered with rHuPH20, and to measure the time to inject the full dose of investigational medicinal product (IMP) of different dose levels of efgartigimod co-administered with a fixed concentration of rHuPH20 by the subcutaneous (SC) route of administration in healthy adult male subjects.
Details
| Lead sponsor | argenx |
|---|---|
| Phase | PHASE1 |
| Status | COMPLETED |
| Enrolment | 33 |
| Start date | Wed Jul 17 2019 00:00:00 GMT+0000 (Coordinated Universal Time) |
| Completion | Thu Sep 26 2019 00:00:00 GMT+0000 (Coordinated Universal Time) |
Conditions
- Healthy Volunteers
Interventions
- ARGX-113 with rHuPH20
Countries
Netherlands