ClinicalTrials.gov record
Active, not recruiting Phase 2 Interventional

A Study Evaluating APG777 in Atopic Dermatitis

ClinicalTrials.gov ID: NCT06395948

Public ClinicalTrials.gov record NCT06395948. 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 May 9, 2026, 7:30 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 Two-part, Multicenter, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Safety and Efficacy of APG777 in Patients With Moderate-to-severe Atopic Dermatitis

Study identification

NCT ID
NCT06395948
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 2
Lead sponsor
Apogee Therapeutics, Inc.
Industry
Enrollment
470 participants

Conditions and interventions

Interventions

  • APG777 Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
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
Apr 28, 2024
Primary completion
Oct 31, 2026
Completion
May 31, 2028
Last update posted
May 7, 2026

2024 – 2028

United States locations

U.S. sites
29
U.S. states
20
U.S. cities
28
Facility City State ZIP Site status
Investigational Site Fountain Valley California 92708
Investigational Site Los Angeles California 90024
Investigational Site San Diego California 92123
Investigational Site New Haven Connecticut 06519
Investigational Site Coral Gables Florida 33134
Investigational Site Jacksonville Florida 32256
Investigational Site Margate Florida 33063
Investigational Site Douglasville Georgia 30135
Investigational Site Chicago Illinois 60657
Investigational Site Skokie Illinois 60077
Investigational Site West Lafayette Indiana 47906
Investigational Site Bowling Green Kentucky 42104
Investigational Site Rockville Maryland 20850
Investigational Site Detroit Michigan 48202
Investigational Site Troy Michigan 48084
Investigational Site Portsmouth New Hampshire 13801
Investigational Site New York New York 10023
Investigational Site Wilmington North Carolina 28403
Investigational Site Boardman Ohio 44512
Investigational Site Mason Ohio 45040
Investigational Site Portland Oregon 97201
Investigational Site Pittsburgh Pennsylvania 15213
Investigational Site Charleston South Carolina 29425
Investigational Site Nashville Tennessee 37215
Investigational Site Dallas Texas 75230
Investigational Site Dallas Texas 75235
Investigational Site San Antonio Texas 78213
Investigational Site Norfolk Virginia 23502
Investigational Site Mill Creek Washington 98012

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 65 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06395948, 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 May 7, 2026 · Synced May 9, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06395948 live on ClinicalTrials.gov.

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