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