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Safety, Tolerability, and Pharmacokinetics of REGN5069 in Healthy Volunteers

NCT03645746 PHASE1 COMPLETED

The primary objective of the study is to evaluate the safety and tolerability of single ascending doses of REGN5069 administered intravenously (IV) and subcutaneously (SC) in healthy male and female participants. The secondary objectives of the study are to characterize the pharmacokinetics (PK) profile of single IV and SC doses of REGN5069 in healthy participants and assess the immunogenicity of REGN5069 in healthy participants administered single IV or SC doses of REGN5069

Details

Lead sponsorRegeneron Pharmaceuticals
PhasePHASE1
StatusCOMPLETED
Enrolment56
Start dateThu Aug 23 2018 00:00:00 GMT+0000 (Coordinated Universal Time)
CompletionMon Sep 30 2019 00:00:00 GMT+0000 (Coordinated Universal Time)

Conditions

Interventions

Countries

Belgium