Long-term Study of APG777 for Atopic Dermatitis

This study is looking at the long-term safety and how well APG777 works for people with moderate-to-severe atopic dermatitis (a chronic skin condition causing itchy rashes). You would be eligible if you have already completed a previous study with APG777 and your doctor believes you would benefit from continuing treatment. The study will give APG777 as an injection under the skin, either every 12 or 24 weeks. Researchers will be tracking any side effects you experience for up to three years to understand the long-term safety of APG777. The study aims to enroll about 350 participants.

Study design
This is a long-term extension study, meaning it follows participants from a previous APG777 study. It is a double-blind study, so neither you nor your doctor will know which treatment schedule you are on. Approximately 350 participants are planned.
What's involved
You would have a screening visit that aligns with your last visit in a previous APG777 study, followed by an extended treatment period and a post-treatment follow-up period. You will also use the same non-prescription moisturizer you used in the prior study.
Compensation
Not stated in the trial record.
Follow-up
Participants will be followed for treatment-emergent adverse events (side effects) for up to 3 years after starting the study.

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NCT07003425

A Long-term Safety and Efficacy Study Evaluating APG777 in Atopic Dermatitis

Recruiting
PHASE2Ages 18+InterventionalTreatment
Apogee Therapeutics, Inc.
~350 participants
Updated 2026-08-21 on ClinicalTrials.gov
What's tested:APG777

At a glance

Recruiting sites
68 of 68 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Number of Participants with Treatment Emergent Adverse Events
Measured over Up to 3 years
Atopic Dermatitis
68 sites across 44 states
Ontario8
Florida3
Texas3
Alberta3
California2
Michigan2
Ohio2
Quebec2

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Eligibility criteria

Inclusion

Participants who have completed the Treatment Period in a prior APG777 study and were, in the Investigator's opinion, compliant with the study protocol
Participants who, in the Investigator's opinion, would benefit from long-term treatment with APG777
Use the same non-prescription non-medicated emollient/moisturizer of their choice from the last day of the Parent Study and throughout the LTE study

Exclusion

Participants who have developed an AE while participating in the Parent Study, which, in the opinion of the Investigator or of the Medical Monitor, could indicate that continued treatment with APG777 may present an unreasonable risk for the patient
Participants who terminated early from the Parent Study or permanently discontinued the study drug during the Parent Study
Use of any of the prohibited medications from Screening Visit (Visit 1) of the LTE study
Presence of dermatologic conditions and/or comorbidities that might confound the diagnosis of AD and/or interfere with study assessments
  • Number of Participants with Treatment Emergent Adverse EventsUp to 3 years