Alopecia Areata Clinical Trial
— AAOfficial title:
A Multicenter, Open-Label, Extension Study to Assess the Long-Term Safety and Efficacy of Jaktinib in Adult Patients With Moderate to Severe Alopecia Areata
This study (Unique Protocol ID: ZGJAK020) as an extension of the ongoing "Study to Evaluate Safety and Efficacy of Jaktinib in Adults With Alopecia Areata (Unique Protocol ID:ZGJAK020)" study. After completion of ZGJAK018 study, the study will be directly extend with an "open-label design".
Status | Recruiting |
Enrollment | 210 |
Est. completion date | December 2024 |
Est. primary completion date | June 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility | Inclusion Criteria: - Subjects voluntarily sign the informed consent form. - Patients who participated in ZGJAK018. Exclusion Criteria: - Subjects who are unsuitable to the trial, as identified by the investigator. |
Country | Name | City | State |
---|---|---|---|
China | 11 Xizhimen South Street | Beijing | Beijing |
Lead Sponsor | Collaborator |
---|---|
Suzhou Zelgen Biopharmaceuticals Co.,Ltd |
China,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Number of subjects reporting treatment-emergent adverse events | Patients with treatment-emergent adverse events/all patients *100% | Baseline through week 24 |
Status | Clinical Trial | Phase | |
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