A Trial of SHR0302 Tablets and SHR0302 Base Gel in Patients With Non-segmental Vitiligo

Recruiting now · Phase 2 · Has a placebo group

Conditions studied: Non-segmental Vitiligo

In brief

The study is being conducted to evaluate the efficacy, and safety of SHR0302 tablets as single therapy or in combination with SHR0302 Base gel for patients with non-segmental vitiligo.

Key facts

Study ID

NCT07251595

Run by

Jiangsu HengRui Medicine Co., Ltd.

People needed

176

Starts

2025-12-05

Expected to finish

2027-09-01

Last updated by the study team

2026-02-18

Who can join

Age: 18 and older, up to 75. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Sign the informed consent form before the clinical trial.
• On the day of signing the informed consent form, the age must be between 18 and 75 years old (inclusive), and it can be either male or female.
• The subjects and their partners had no intention of having children during the study period and within one month after the administration of the drug, did not donate sperm or eggs, and voluntarily adopted effective contraceptive measures. The serum pregnancy test results of the female subjects must be negative and they must not be in the lactation period.
• During the screening process, it was clinically diagnosed as non-segmental vitiligo.
• Throughout the entire research process, the participants agreed to stop using all treatments related to vitiligo as well as any cosmetic products with therapeutic effects.

You may not qualify if…

• Subjects diagnosed with segmental, mixed or undifferentiated vitiligo; or subjects previously diagnosed with other skin pigmentation disorders.
• When the facial skin lesions caused by vitiligo cover more than 33% of the area with white hair.
• During the screening period or at the baseline, there were other active skin lesions or skin infections that might interfere with the use of the study drug or the evaluation of the drug's efficacy.
• Subjects with a history of related infections/communicable diseases or infection/contagion history.
• Known or suspected history of immunosuppression.
• Tuberculosis (TB) or latent tuberculosis infection.
• Positive for human immunodeficiency virus antibody HIV-Ab, positive for syphilis-specific antibody, positive for hepatitis C virus antibody HCV-Ab, or hepatitis B virus (HBV) infection.
• Subjects who have malignant tumors or have a history of malignant tumors.
• Abnormal thyroid function, with a history of thrombotic diseases within the previous 12 months, and having experienced a cardiovascular or cerebrovascular event that required hospitalization within the previous 12 months.
• There are serious abnormalities in the cardiovascular, mental, renal, liver, immune, gastrointestinal, urogenital, nervous, skeletal-muscular, skin, sensory, endocrine or hematological systems.
• Pregnant women, lactating women, or female participants who plan to become pregnant during the study period.
• Those who are known to be allergic to the test drug or any component of the test drug.

Where it is running

• Dermatology Hospital affiliated to Shandong First Medical University — Jinan, Shandong, China (enrolling)

Full record on ClinicalTrials.gov

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