drugset / Trial / NCT04571424

A Study to Evaluate Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of BIIB133 (Dapirolizumab Pegol) in Healthy Japanese and Caucasian Participants

NCT04571424 ↗

Phase 1 Completed 33 enrolled Biogen
RandomizedSequentialQuadruple-blindTreatment

Summary

The primary objective of the study is to assess the safety and tolerability of a single intravenous (IV) dose of dapirolizumab pegol (DZP) in Japanese healthy study participants compared with those of Caucasian healthy study participants. The secondary objectives of the study are to assess the pharmacokinetic(s) (PK) of a single IV dose of DZP in Japanese and Caucasian healthy study participants, to evaluate ethnic sensitivity on the PK of DZP between body weight- and gender-matched Japanese and Caucasian healthy study participants and to evaluate the immunogenicity of a single IV dose of DZP in Japanese and Caucasian healthy study participants.

Timeline

Start
2020-10-14
Primary completion
2021-04-08
Completion
2021-04-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Dapirolizumab pegol Monoclonal antibody — Intravenous

Indications

No indication recorded.