Status:
TERMINATED
Assess the Efficacy and Safety of SHR0302 Ointment in Adult Patients With Vitiligo
Lead Sponsor:
Reistone Biopharma Company Limited
Conditions:
Vitiligo
Eligibility:
All Genders
18-65 years
Phase:
PHASE2
PHASE3
Brief Summary
The purpose of this study is to assess the efficacy and safety of SHR0302 ointment in adult patients with Vitiligo.
Detailed Description
This study is a phase II/Ⅲ seamless adaptive clinical trial to evaluate the efficacy and safety of SHR0302 ointment in adult patients with non-segmental vitiligo.
Eligibility Criteria
Inclusion
- Subjects who voluntarily signed an informed consent form.
- Ages at ≥18 and ≤ 65 years
- Clinical diagnosis of non-segmental vitiligo.
- All women and men who are likely to give birth must be willing to use at least one efficient method of contraception from the signing of the informed consent form to 1 month after the last dose of IP.
- Subjects who agree to discontinue all vitiligo-related treatments and camouflage cosmetics with therapeutic effect between screening visit and the last follow-up visit.
- Subjects who are willing and able to comply with the scheduled visits and treatment plan, laboratory testing and other study procedures.
Exclusion
- Subjects who were diagnosed with segmental vitiligo, mixed vitiligo or unclassified vitiligo.
- Subjects with historical or current evidence of clinically significant disease or lab test abnormalities or with disease that require the administration of prohibited drugs in this study.
- Subjects with a malignant tumor or a history of malignant tumor (except for fully treated or resected skin non-metastatic basal cell carcinoma or squamous cell carcinoma).
- Pregnant or lactating female subjects;
- Subjects who have previously received JAK inhibitors therapy, systemic or oral
- Subjects who had used any biologics within12 weeks before the baseline or 5 half-lives (whichever is longer).
- Subjects who participated in other interventional clinical studies within 4 weeks before the baseline visit, or who were still within 5 half-lives of the last dose of the intervention clinical study drug at baseline.
- Subjects who received a live or live-attenuated vaccination within 8 weeks before the baseline visit.
- Any other condition that causes the subject to be unfit for the study as per discretion of the investigator.
Key Trial Info
Start Date :
January 29 2020
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
March 21 2022
Estimated Enrollment :
75 Patients enrolled
Trial Details
Trial ID
NCT04774809
Start Date
January 29 2020
End Date
March 21 2022
Last Update
July 13 2022
Active Locations (16)
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1
The First Affiliated Hospital of Fujian Medical University
Fuzhou, Fujian, China
2
Dermatology Hospital of Southern Medical University
Guangzhou, Guangdong, China
3
Wuhan No.1 Hospital
Wuhan, Hubei, China
4
The First Affiliated Hospital of Dalian Medical University
Dalian, Liaoning, China