drugset / Trial / NCT06716879

A Study to Evaluate Safety, Tolerability, and Pharmacokinetics of a Single Dose of Donzakimig in Healthy Chinese and Japanese Participants

NCT06716879 ↗

Phase 1 Completed 32 enrolled UCB Biopharma SRL
RandomizedParallel-groupDouble-blindBasic science

Summary

The purpose of the study is to investigate the safety, tolerability, and pharmacokinetic parameters of 2 dose strengths of donzakimig, each administered subcutaneously as a single dose, in healthy Chinese and Japanese study participants.

Timeline

Start
2024-12-06
Primary completion
2025-04-04
Completion
2025-04-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Donzakimig Monoclonal antibody — Subcutaneous

Indications

No indication recorded.