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Completed Phase 1Phase 2 Interventional Accepts healthy volunteers

A Single-ascending Dose (Part A) and Repeat-dose (Part B) Study to Investigate the Safety, Pharmacokinetics and Efficacy (Part B Only) of UCB1381 in Healthy Study Participants (Part A) and in Study Participants With Moderate to Severe Atopic Dermatitis (Part B)

ClinicalTrials.gov ID: NCT05277571

Public ClinicalTrials.gov record NCT05277571. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 21, 2026, 6:49 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 1/2A, Randomized, Placebo-Controlled, Single-Ascending Dose (Part A, Participant- and Investigator-Blind) and Repeat-Dose (Part B, Participant-, Investigator-, and Sponsor-Blind) Study to Investigate the Safety, Pharmacokinetics, and Efficacy (Part B Only) of UCB1381 in Healthy Study Participants (Part A) and in Study Participants With Moderate to Severe Atopic Dermatitis (Part B)

Study identification

NCT ID
NCT05277571
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
UCB Biopharma SRL
Industry
Enrollment
109 participants

Conditions and interventions

Interventions

  • UCB1381 Biological
  • Placebo Drug

Biological · Drug

Eligibility (public fields only)

Age range
18 Years to 65 Years
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 6, 2022
Primary completion
Jul 16, 2025
Completion
Sep 18, 2025
Last update posted
Jun 24, 2026

2022 – 2025

United States locations

U.S. sites
16
U.S. states
8
U.S. cities
16
Facility City State ZIP Site status
Up0110 125 Beverly Hills California 90212
Up0110 101 Glendale California 91206
Up0110 116 Los Angeles California 90045
Up0110 121 Northridge California 91324
Up0110 126 Tustin California 92780
Up0110 127 Valencia California 91355
Up0110 108 Clearwater Florida 33765
Up0110 109 Miami Lakes Florida 33014
Up0110 106 Ocala Florida 34471
Up0110 102 St. Petersburg Florida 33705
Up0110 111 College Park Georgia 30349
Up0110 114 Minneapolis Minnesota 55455
Up0110 107 New York New York 10029
Up0110 124 Winston-Salem North Carolina 27103
Up0110 104 Oklahoma City Oklahoma 73170
Up0110 119 Philadelphia Pennsylvania 19103

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05277571, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 24, 2026 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05277571 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →