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A Study to Assess the Safety and Pharmacokinetics of a Single Dose of UCB9741 in Healthy Caucasian and Japanese Participants - Trial NCT06315335

Access comprehensive clinical trial information for NCT06315335 through Pure Global AI's free database. This Phase 1 trial is sponsored by UCB Biopharma SRL and is currently Not yet recruiting. The study focuses on Healthy Participants. Target enrollment is 50 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.

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NCT06315335
Phase 1
Not yet recruiting
drug
Trial Details
ClinicalTrials.gov โ€ข NCT06315335
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A Study to Assess the Safety and Pharmacokinetics of a Single Dose of UCB9741 in Healthy Caucasian and Japanese Participants
A SINGLE CENTER, RANDOMIZED, INVESTIGATOR- AND PARTICIPANT-BLIND, PLACEBO-CONTROLLED, PARALLEL-GROUP, ETHNOBRIDGING PHASE 1 STUDY TO EVALUATE SAFETY, TOLERABILITY, AND PHARMACOKINETICS AFTER SINGLE-DOSE OF UCB9741 IN HEALTHY CAUCASIAN AND JAPANESE PARTICIPANTS

Study Focus

Healthy Participants

UCB9741

Interventional

drug

Sponsor & Location

UCB Biopharma SRL

UCB Pharma

Timeline & Enrollment

Phase 1

Jul 01, 2024

Jul 29, 2025

50 participants

Primary Outcome

Occurrence of TEAEs,Occurrence of treatment-emergent SAEs

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.

ICD-10 Classifications

Seeking and accepting physical, nutritional and chemical interventions known to be hazardous and harmful
Healthy person accompanying sick person
Routine general health check-up of sports teams
Obesity
Persons with potential health hazards related to communicable diseases

Data Source

ClinicalTrials.gov

NCT06315335

Non-Device Trial