CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 794 enrolled
Drug / intervention
Tralokinumab +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03160885
NCT03160885Phase 3Completed

A Randomised, Double-blind, Placebo-controlled, Phase 3 Trial to Evaluate the Efficacy and Safety of Tralokinumab Monotherapy in Subjects With Moderate to Severe Atopic Dermatitis Who Are Candidates for Systemic Therapy

LEO Pharma·interventional·Posted May 19, 2017·Updated Mar 11, 2025

In Brief

A Phase 3 clinical trial evaluating Tralokinumab and Placebo for Atopic Dermatitis. Completed, enrolled 794 participants across 115 sites in 9 countries.

Detailed Summary

Primary objective: To evaluate the efficacy of tralokinumab compared with placebo in treating moderate to severe atopic dermatitis (AD). Secondary objectives: To evaluate the efficacy of tralokinumab on severity and extent of AD, itch, and health related quality of life compared with placebo. Maintenance objective: To evaluate maintenance of effect with continued tralokinumab dosing up to 52 weeks compared to placebo for subjects achieving clinical response at Week 16.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesAustralia, Canada, Denmark, Italy, Poland, Russia, South Korea, United Kingdom, United States
Collaborators--

Timeline

Phase 3CompletedFinished
201820192020202120222023202420252026
First PostedMay 19, 2017
Enrollment StartJun 12, 2017
Primary CompletionSep 4, 2018
Study CompletionAug 14, 2019
TodayJul 2, 2026
Enrollment to primary: 1.2 yearsPosted 9.1 years ago

Interventions

Tralokinumabdrug

Tralokinumab is a human recombinant monoclonal antibody of the IgG4 subclass that specifically binds to human IL-13 and blocks interaction with the IL-13 receptors. It is presented as a liquid formulation for subcutaneous (SC) administration

Placebodrug

Placebo contains the same excipients, in the same concentration only lacking tralokinumab