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Terminated Phase 2 Interventional Results available

A Study to Evaluate the Safety and Tolerability of MOR106 Administered Concomitantly With Topical Corticosteroids, in Adult Participants With Moderate to Severe Atopic Dermatitis

ClinicalTrials.gov ID: NCT03864627

Public ClinicalTrials.gov record NCT03864627. 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 Oct 28, 2026, 1:06 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 Randomized, Double-blind, Placebo-controlled, Multicentre Phase 2 Study to Evaluate the Safety and Tolerability of Subcutaneous MOR106 Administered Concomitantly With Topical Corticosteroids for Eight Weeks, in Adult Subjects With Moderate to Severe Atopic Dermatitis

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

To investigate the safety and tolerability of repeated subcutaneous (s.c.) doses of MOR106 administered concomitantly with topical corticosteroids (TCS) in participants with moderate to severe atopic dermatitis (AD) who are candidates for systemic therapy.

Study identification

NCT ID
NCT03864627
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Lakefront Biotherapeutics NV
Industry
Enrollment
33 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 65 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

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

Study timeline

Start date
Mar 25, 2019 (Actual)
Primary completion
Feb 27, 2020 (Actual)
Completion
Feb 27, 2020 (Actual)
Last update posted
Jan 5, 2021

2019 – 2020

United States locations

U.S. sites
14
U.S. states
7
U.S. cities
14
Facility City State ZIP Site status
First OC Dermatology Fountain Valley California 92708 —
Marvel Research, LLC Huntington Beach California 92647 —
LA Universal Research Center, Inc. Los Angeles California 90057 —
MedDerm Associates San Diego California 92103 —
Encore Medical Research Hollywood Florida 33021 —
Advanced Research Institute of Miami LLC Homestead Florida 33030 —
Vista Health Research Miami Florida 33185 —
Arlington Dermatology Rolling Meadows Illinois 60008 —
Dawes Fretzin Clinical Research Group, LLC Indianapolis Indiana 46250 —
DS Research Louisville Kentucky 40241 —
Greenwich Village Dermatology New York New York 10012 —
Center for Clinical Studies Houston Texas 77004 —
Progressive Clinical Research San Antonio Texas 78229 —
Center for Clinical Studies Webster Texas 77598 —

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 NCT03864627, 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 Jan 5, 2021 · Synced Oct 28, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03864627 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →