IL-4 and Insulin Resistance for Treatment of Patients with Atopic Dermatitis

Overview

Información sobre este estudio

The objective of this study is to assess the metabolic effect of systemic inhibition of IL-4 signaling on insulin sensitivity in patients with atopic dermatitis by comparing in vivo evaluations of insulin sensitivity in subjects on dupilumab vs. subjects matched for similar adiposity, with atopic dermatitis, but without dupilumab therapy.

 

Elegibilidad para la participación

Los requisitos de elegibilidad de los participantes incluyen la edad, el sexo, el tipo y el estadio de la enfermedad, y los problemas de salud o tratamientos previos. Las pautas difieren de un estudio a otro e identifican quiénes pueden o no pueden participar. No hay garantía de que cada persona elegible que desee participar en un ensayo se inscribirá. Comunícate con el equipo del estudio para analizar la elegibilidad del estudio y la posible participación.

Inclusion Criteria:

- Ability to sign informed consent form.

- Body mass index (BMI), 22-29 kg/m^2.

- Diagnosis of Atopic Dermatitis treated with dupilumab for longer than 6 months.

- Diagnosis of Atopic Dermatitis treated with topical steroids or phototherapy.

Exclusion Criteria:

- Any prescription for systemic glucocorticoid, immunosuppressant, antidiabetic
medications in the past 6 months.

- Evidence of diabetes mellitus.

- Morning Cortisol < 5 mg/dl (collected before 10.30 am).

- Presence of acute illness.

- Low hemoglobin or hematocrit.

- Current participation in a weight-loss regimen, with a weight loss > 10% total body
weight in the last 6 months).

- Smoking history in the last 6 months (tobacco, nicotine-containing products including
e-cigarettes).

- Pregnant or breastfeeding.

- Personal history of gastric bypass surgery.

- Previous participation in a clinical trial with an investigational product in the past
30 days, or 5 half-lives, or twice the duration of the biological effect of the
investigational drug (whichever is longest).

- Exposed to more than 4 new chemical entities within 12 months before study enrollment.

- Any other condition or event considered exclusionary by the PI and the study
physician.

Note: Other protocol defined Inclusion/Exclusion criteria may apply.

Eligibility last updated 11/10/22. Questions regarding updates should be directed to the study team contact.

Sedes participantes de Mayo Clinic

Los estatus de los estudios cambian con frecuencia. Comunícate con el equipo del estudio para obtener la información más actualizada acerca de la posibilidad de participar.

Sede de Mayo Clinic Estatus

Scottsdale/Phoenix, Ariz.

Investigador principal de Mayo Clinic

Elena Anna De Filippis, M.D., Ph.D.

Cerrado para la inscripción

More information

Publicaciones

Publications are currently not available
.
CLS-20532381

Mayo Clinic Footer