drugset / Trial / NCT06970301

A Study to Assess the Safety and Tolerability, and Pharmacokinetics of UCB0022 in Healthy Caucasian, Japanese, and Chinese Participants

NCT06970301 ↗

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

Summary

The primary purpose of this study is to assess the safety and tolerability of oral glovadalen (UCB0022) in healthy Caucasian, Japanese, and Chinese participants.

Timeline

Start
2025-04-28
Primary completion
2026-05-29
Completion
2026-05-29

Drugs

EvaluationDrugModalityDoseRoute
Subject glovadalen Small molecule — Oral

Indications

No indication recorded.