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Clinical Trials in the USA / NCT07748169
Starting soon Observational

An Observational Study of Patients With Dermatologic Disease

NCT07748169 · tracked via the Priya Life Science USA tracker
Sponsor
Target PharmaSolutions, Inc.
Phase
Observational
Started
2026-09
Last updated
2026-09-10

Condition(s) studied

VitiligoAtopic DermatitisAlopecia AreataHidradenitis Suppurativa (HS)

Study summary

TARGET-DERM+ is an observational research study to conduct a comprehensive review of outcomes for patients with dermatologic disease (DD) and providers who treat these patients. The study includes patients managed for DD of any etiology in usual clinical practice in the United States and addresses important clinical questions regarding the management of DD by collecting and analyzing data from patients at academic medical centers and community medical practices and/or data from providers who treat them.

Eligibility

Sex
ALL
Min age
Max age
Healthy volunteers
No
Inclusion Criteria: * Adult or pediatric participants managed for DD invited to participate OR a provider who treats patients with these conditions. Informed consent is required for all Engaged Cohort participants. * Adult or pediatric participants at the time of enrollment with a diagnosis of DD by ICD code or other relevant healthcare code as part of the EHR interface. Exclusion Criteria: * Participant withdrew consent; Failure to complete activities as required per the cohort clarification letter.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Greenwich Village Dermatology New York New York

More Target PharmaSolutions, Inc. trials in the USA

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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 NCT07748169 on ClinicalTrials.gov ↗ ← All trials in the USA