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Recruiting Phase 2 NCT06771063

A Study of the Efficacy and Safety of WXSH0102 in Treating VCC Patients

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Trial Parameters

Condition Vaginitis
Sponsor Cisen Pharmaceutical CO., LTD.
Study Type INTERVENTIONAL
Phase Phase 2
Enrollment 108
Sex FEMALE
Min Age 18 Years
Max Age 64 Years
Start Date 2025-01-13
Completion 2025-07-10
Interventions
WXSH0102/placebofluconazole capsules/placebo

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Brief Summary

This study is a multicenter, randomized, double-blind, active-controlled, dose-ranging clinical trial designed to evaluate the efficacy and safety of the investigational drug compared to the active comparator in the treatment of vulvovaginal candidiasis. The trial consists of three phases: screening/enrollment (D-3 to D-1), treatment period (D1 to D3), and follow-up period (D4, D11±2, D25±3). Eligible subjects in this study will be randomized in a 1:1:1:1 ratio to three investigational drug arms with different dosing regimens and one active control arm. Specifically, Group A will receive WXSH0102 tablets with 1400 mg on the first day followed by a maintenance dose of 700 mg for two consecutive days, Group B will receive WXSH0102 tablets with 1000 mg on the first day followed by a maintenance dose of 500 mg for two consecutive days, Group C will receive WXSH0102 tablets with 600 mg on the first day followed by a maintenance dose of 300 mg for two consecutive days, and Group D (active control group) will receive fluconazole capsules for only one day on D1. All medications will be administered orally.

Eligibility Criteria

Inclusion Criteria: * The subjects understood and voluntarily signed the informed consent Form (ICF), and were willing and able to comply with the study protocol. * Female participants who signed ICF at the age of 18-64 years (including the cut-off value) and had sexual intercourse; * Participants were diagnosed with VVC and met each of the following criteria: a. At screening, the total score on the VVC scale was ≥4 and at least two of the symptoms or signs on the VVC scale were present; b. A vaginal discharge sample collected at screening was Gram stain positive for Candida (hypha/pseudohypha/budding); c. Vaginal pH ≤4.5; Symptoms: vulvovaginal itching, vulvar burning pain, dyspareunia and urination pain, excessive secretion, secretion is tofu residue like; Physical signs: gynecological examination showed vulvar hyperemia and edema, which may be accompanied by scratches. In severe cases, chapped skin, exfoliation and even erosion could be seen. Vaginal mucosa was hyperemic, vaginal se

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