Treatment of Moderate-to-Severe Atopic Dermatitis With Ivarmacitinib in Adolescents and Adults

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age12-75
SponsorXiangya Hospital of Central South University

About this trial

Atopic dermatitis (AD) is a skin condition characterized by a rash and itching, resulting from skin inflammation. Ivarmacitinib is an approved medication for treating AD.

This study aims to evaluate the effectiveness and safety of Ivarmacitinib in the treatment of moderate-to-severe atopic dermatitis under real-world conditions. It will assess the time to pruritus improvement and skin lesion clearance, collect large-sample safety data, analyze disease improvement across patient subgroups with different baseline characteristics, and explore the impact of various maintenance treatment regimens on disease recurrence.

It is expected that there will be no additional burden for participants in this trial.

Eligibility criteria

Qualifiers

Aged between 12 and 75 years;

Diagnosed with moderate-to-severe atopic dermatitis (AD) ;

Participants (and legal representatives for adolescents) able to understand and communicate with the investigator.

Disqualifiers

Absolute lymphocyte count of <0.50 x 10^9 /L (<500/mm3);

Absolute Neutrophil Count (ANC) of <1 X 10^9/L (<1000/mm3);

Hemoglobin level < 80 g/L.

Subject has any malignancies or has a history of malignancies with the exception of adequately treated or excised non-metastatic basal cell or squamous cell cancer of the skin, or cervical carcinoma in situ.

Trial design

Treatments tested in this trial

  • Ivarmacitinib Sulfate Tablets

Treatment groups

1,000 Participants
are divided into 1 treatment group

Locations

This trial has no locations