drugset / Trial / NCT06315335

A Study to Assess the Safety and Pharmacokinetics of a Single Dose of UCB9741 in Healthy Caucasian and Japanese Participants

NCT06315335 ↗

Phase 1 Completed 40 enrolled UCB Biopharma SRL
RandomizedParallel-groupDouble-blindOther

Summary

The purpose of the study is investigate the safety, tolerability and pharmacokinetic of UCB9741 after 2 dose strengths administered subcutaneous as a single-dose in healthy Caucasian and Japanese participants.

Timeline

Start
2024-07-01
Primary completion
2025-01-01
Completion
2025-01-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Galvokimig Monoclonal antibody — Subcutaneous

Indications

No indication recorded.