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

Part of paid clinical trials in Lancaster, California.

Sponsor
Inmagene LLC
Study ID
NCT07734415
Phase
PHASE2
Status
Enrolling By Invitation

Conditions

Eligibility Criteria

Sex
ALL
Age
18 Years - 75 Years
Healthy Volunteers
Not accepted

Interventions

  • IMG-007 — DRUG
    Participants will receive IMG-007 subcutaneously.

Study Details

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)

Key Dates

First listed
Jul 29, 2026
Start date
Jun 5, 2026
Status verified
Jul 2026
Primary completion
Mar 31, 2028
Completion
Mar 31, 2028

Study Design

Enrollment
400 participants (estimated)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT

Arms

  • Experimental: IMG-007 Dose
    Subcutaneous injection as per protocol.

Primary Outcome Measure

Evaluate the safety of long-term treatment with IMG-007 in participants with moderate-to-severe atopic dermatitis [ Time Frame: Baseline, Week 44 ]

Locations (16)

FacilityCityStateZIPSite coordinators
Inmagene Site 1LancasterCalifornia93534-
Inmagene Site 23Los AngelesCalifornia90095-
Inmagene Site 19OcalaFlorida34470-
Inmagene Site 4TampaFlorida33609-
Inmagene Site 2Rolling MeadowsIllinois60008-
Inmagene Site 6Kew GardensNew York11415-
Inmagene Site 21New YorkNew York10029-
Inmagene Site 11WoodburyNew York11797-
Inmagene Site 20CharlotteNorth Carolina28277-
Inmagene Site 10FargoNorth Dakota58103-
Inmagene Site 9ColumbusOhio43213-
Inmagene Site 5Mayfield HeightsOhio44124-
Inmagene Site 3PortlandOregon97210-
Inmagene Site 12AndersonSouth Carolina29621-
Inmagene Site 8SouthlakeTexas76092-
Inmagene Site 7BurienWashington698168-

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