A Longitudinal Observational Study of Patients Undergoing Therapy for IMISC (TARGET-DERM)

Target PharmaSolutions

Status: Enrolling

Conditions: Atopic Dermatitis; Psoriasis; Vitiligo; Chronic Spontaneous Urticaria; Hidradenitis Suppurativa; Alopecia Areata

Study type: Observational

Funder types: Industry

Identifiers

NCT03661866

TARGET-DERM

Details and patient eligibility

About

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.

Full 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.

Enrollment: 15,000 estimated patients

Sex: All

Volunteers: No Healthy Volunteers

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).