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Enrolling by invitation Phase 2

Long-term Safety and Efficacy Evaluation of IMG-007 in Participants With Moderate-to-Severe Atopic Dermatitis

NCT07734415 · tracked via the Priya Life Science USA tracker
Sponsor
Inmagene LLC
Phase
Phase 2
Started
2026-06-05
Last updated
2026-07-29

Condition(s) studied

Atopic DermatitisAtopic Dermatitis EczemaEczema

Investigational drug(s) / intervention(s)

IMG-007 →

IMG-007: Participants will receive IMG-007 subcutaneously.

Study summary

The purpose of this study is to evaluate the safety and efficacy of long-term treatment with IMG-007 in participants with moderate-to-severe atopic dermatitis (AD)

Eligibility

Sex
ALL
Min age
18 Years
Max age
75 Years
Healthy volunteers
No
Enrolling by invitation participants with moderate to severe AD who have completed IMG-007-203

Primary outcome measure(s)

  • Evaluate the safety of long-term treatment with IMG-007 in participants with moderate-to-severe atopic dermatitis — Baseline, Week 44
    Incidence and severity of TEAEs, including treatment-emergent SAEs, AESIs, and AEs leading to discontinuation

Trial sites (23)

FacilityCityRegionStatus
Inmagene Site 1 Lancaster California
Inmagene Site 23 Los Angeles California
Inmagene Site 19 Ocala Florida
Inmagene Site 4 Tampa Florida
Inmagene Site 2 Rolling Meadows Illinois
Inmagene Site 6 Kew Gardens New York
Inmagene Site 21 New York New York
Inmagene Site 11 Woodbury New York
Inmagene Site 20 Charlotte North Carolina
Inmagene Site 10 Fargo North Dakota
Inmagene Site 9 Columbus Ohio
Inmagene Site 5 Mayfield Heights Ohio
Inmagene Site 3 Portland Oregon
Inmagene Site 12 Anderson South Carolina
Inmagene Site 8 Southlake Texas
Inmagene Site 7 Burien Washington
Inmagene Site 15 Surrey British Columbia
Inmagene Site 22 Vancouver British Columbia
Inmagene Site 17 Greater Sudbury Ontario
Inmagene Site 13 Mississauga Ontario
Inmagene Site 18 North Bay Ontario
Inmagene Site 14 Montreal Quebec
Inmagene Site 16 Saskatoon Saskatchewan
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07734415 on ClinicalTrials.gov ↗ ← All trials in the USA