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Efgartigimod Co-administered Subcutaneously With rHuPH20 in Healthy Subjects

NCT04073589 PHASE1 COMPLETED

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 sponsorargenx
PhasePHASE1
StatusCOMPLETED
Enrolment33
Start dateWed Jul 17 2019 00:00:00 GMT+0000 (Coordinated Universal Time)
CompletionThu Sep 26 2019 00:00:00 GMT+0000 (Coordinated Universal Time)

Conditions

Interventions

Countries

Netherlands