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Not yet taking people in ChinaPhase 3

Tests stapokibatrt in children with atopic dermatitis

Tests the drug stapokibatrt in children aged 2 to 12 with atopic dermatitis.

Plain-language title generated from the registry record
Registry title: A Study of Stapokibatrt in Children Subjects With Atopic Dermatitis

Key facts

Where
Beijing, ChinaSee the site
Phase
Phase 3

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 2 and 12 years old?

Source: NCT07106372, who can take part

Where in China

  • Beijing Children's Hospital, Capital Medical UniversityBeijing, ChinaNo longer taking part

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Keymed Biosciences Co.Ltd
Trial code
NCT07106372
Record updated
6 August 2025
Original description
This is a multi-center, single-arm, open-label phase 3 study to evaluate the safety, efficacy, Pharmacokinetics(PK) and immunogenicity of Stapokibatrt in children with Atopic Dermatitis.Read full original descriptionShow less

A Multi-center, Single-arm, Open-label Study to Evaluate the Safety and Efficacy of Stapokibatrt in Children With Atopic Dermatitis

This is a multi-center, single-arm, open-label phase 3 study to evaluate the safety, efficacy, Pharmacokinetics(PK) and immunogenicity of Stapokibatrt in children with Atopic Dermatitis.

Inclusion: Voluntarily participate in the continuing study and sign the written Informed Consent Form(ICF); Subjects who must complete the evaluation of Week 18 of the main study; Have the ability to communicate well with the researcher and comply with the follow-up visits of the protocol.

Exclusion: Planned major surgical procedure during the patient's participation in this study; Any other circumstances in which the researcher deems not suitable to participate in this study.

ClinicalTrials.gov NCT07106372