Clinical Trials Study

N/A

A Longitudinal Observational Study of Patients Undergoing Therapy for IMISC

Conditions: ATOPIC DERMATITIS, ALOPECIA AREATA, HIDRADENITIS SUPPURATIVA, VITILIGO, PSORIASIS, CHRONIC SPONTANEOUS URTICARIA

Study #:
NCT03661866
Last Updated:
03/20/2026
Recruitment Status:
Active, not recruiting
Estimated Study Completion Date:
12/01/2050

Summary

TARGET-DERM is a longitudinal, observational study of adult and pediatric patients being managed for Atopic Dermatitis and other Immune-Mediated Inflammatory Skin Conditions (IMISC) in usual clinical practice. TARGET-DERM will create a research registry of patients with IMISC within academic and community real-world practices in order to assess the safety and effectiveness of current and future therapies.

Age: All ages

Gender: All

Start Date: 12/21/2018

Primary Completion Date (Estimated): 12/01/2050

Study Completion Date (Estimated): 12/01/2050

Accepts Healthy Volunteers: No

Trial Purpose and Description

TARGET-DERM is a longitudinal, observational study of adult and pediatric patients being managed for Atopic Dermatitis and other Immune-Mediated Inflammatory Skin Conditions (IMISC) in usual clinical practice. TARGET-DERM will create a research registry of patients with IMISC within academic and community real-world practices in order to assess the safety and effectiveness of current and future therapies. The duration of follow-up for participants enrolled in the EU is limited to 5-years. Those within in US and Canada may consent to indefinite follow-up.

Eligibility Criteria

Age: All ages

Gender: All

Accepts Healthy Volunteers: No

Inclusion criteria:

* 1\. Adults and children (all ages) with Atopic Dermatitis or other Immune-mediated Inflammatory Skin Conditions been prescribed any dermatologic treatment.

* 2\. Participant has plans for future visits at the site for continued management of IMISC.

Exclusion criteria:

* 1\. Inability to provide written informed consent/assent.

* 2\. Subjects participating in any interventional study or trial for IMISC treatment trial at the time of enrollment. Patients may be enrolled in TARGET-DERM once participation in the trial is complete. Note: Participants may be enrolled in other registries or studies where IMISC treatment outcomes are observed and/or reported (such as center-based registries).

Principal Investigator

Holly Kanavy, DO

For more information about this study, contact:

Holly Kanavy

866-633-8255 / 718-230-2997 / 510-996-0741

HKanavy@montefiore.org