drugset / Trial / NCT06555601

A First-in-human Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of UCB3101 in Healthy Participants

NCT06555601 ↗

Phase 1 Terminated 56 enrolled UCB Biopharma SRL
RandomizedSequentialTriple-blindBasic science

Summary

The purpose of the study is to evaluate the safety and tolerability of a single ascending dose of UCB3101 in cohorts of healthy male and female study participants.

Timeline

Start
2024-07-31
Primary completion
2025-11-24
Completion
2025-11-24

Outcome

Outcome not reported

Stopped (Business): “sponsor decision”

Drugs

EvaluationDrugModalityDoseRoute
Subject UCB3101 Unknown — —

Indications

No indication recorded.