A Study of Stapokibart Injection in Patients With Atopic Dermatitis (AD) (NCT07544862) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
A Study of Stapokibart Injection in Patients With Atopic Dermatitis (AD)
China1,000 participantsStarted 2026-06
Plain-language summary
This study is an open label, prospective study to evaluate the safety and efficacy of Stapokibart Injection in patients with AD.
Who can participate
Age range18 Years
SexALL
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Inclusion Criteria:
* Trial participants aged 18 years or older at baseline, with no restrictions on gender.
* Physician decision to treat trial participants with Stapokibart Injection for AD (according to the China-specific prescribing information) made prior to and independently of the participant's participation in the study.
Exclusion Criteria:
* Known history of allergic reaction to Stapokibart Injection.
* Trial participants currently or plan participating in any interventional clinical trial.
* Trial participants with hematologic malignancies.
* Women with pregnant.
* Any condition that, in the opinion of the investigator, may interfere with trial participants' ability to participate in the study.
What they're measuring
1
The incidence rate of adverse reactions
Timeframe: From enrollment to the end of treatment at 52 weeks.