Skip to content
Study details
Enrolling now

A Study to Evaluate the Efficacy and Safety of IMG-007 in Adult Participants With Moderate-to-Severe Atopic Dermatitis

Inmagene LLC
NCT IDNCT07037901ClinicalTrials.gov data as of Apr 2026
Phase

Phase 2

Target enrollment

220

Study length

about 2.4 years

Ages

18–74

Locations

16 sites in CA, FL, IL +8

What this study is about

Researchers are testing a treatment called IMG-007 compared to a placebo for adults with moderate-to-severe atopic dermatitis. The trial will last 866 days, and the goal is to enroll 220 participants.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Take IMG-007
  • 2.Take Placebo

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Standard

How treatment is administered

Treatment Assignment
Randomized & Blinded

You may get a placebo/standard care, and you won't know which.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Endpoints

Primary: Mean percent change from baseline in EASI at Week 20

Secondary: Incidence and severity of TEAE including treatment-emergent SAEs, Mean percent change from baseline in EASI at Week 16

Body systems

Dermatology