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

Phase 2

Recruiting

• Conditions: Vaginitis
• Interventions: Drug: WXSH0102/placebo; Drug: fluconazole capsules/placebo

• Registration Number: NCT06771063
• Lead Sponsor: Cisen Pharmaceutical CO., LTD.

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.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2024-12-25
• Study First Submitted QC: 2025-01-07
• Study Start: 2025-01-13
• Study First Posted: 2025-01-13
• Status Verified: 2025-02
• Last Update Submitted: 2025-02-11
• Last Update Posted: 2025-02-13
• Primary Completion: 2025-07-10
• Study Completion: 2025-07-31

Recruitment & Eligibility

• Status: RECRUITING
• Sex: Female
• Target Recruitment: 108

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 secretion was curd or tofu residue like;
• Subjects who are capable of oral administration;
• For the duration of the study, participants agreed to abstain from sexual activity and to use the condom throughout sexual activity.

Exclusion Criteria

• Known or suspected allergic history to any component of this product, fluconazole or pyrrole drugs;
• Subjects with any vulvovaginal or cervical disease that may affect the diagnosis and evaluation of VVC;
• Topical or systemic antifungal treatment for VVC within 14 days before randomization;
• Significant liver disease or abnormal liver function tests (alanine aminotransferase [ALT], aspartate aminotransferase [AST] > 1.5 ULN); Patients with severe renal disease or renal insufficiency (glomerular filtration rate (GFR) < 60ml/min/1.73m2 );
• Patients who planned to undergo treatment or surgery for vulvar, vaginal or cervical lesions during the study period;
• Severe gastrointestinal disease or other conditions that may affect the absorption of the trial drug;
• Patients with severe heart, lung, liver, kidney dysfunction and hematopoietic system diseases;

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Arm A : WXSH0102 Day1 1400 mg Day2-3 700	WXSH0102/placebo	Arm A will receive WXSH0102 tablets with a loading dose of 1400 mg on the first day followed by a maintenance dose of 700 mg for two consecutive days
Arm B : WXSH0102 Day1 1000 mg Day2-3 500 arm	WXSH0102/placebo	Arm B will receive WXSH0102 tablets with a loading dose of 1000 mg on the first day followed by a maintenance dose of 500 mg for two consecutive days
C : WXSH0102 Day1 600 mg Day2-3 300	WXSH0102/placebo	Arm C will receive WXSH0102 tablets with a loading dose of 600 mg on the first day followed by a maintenance dose of 300 mg for two consecutive days
Arm D: fluconazole	fluconazole capsules/placebo	Arm D (active control group) will receive fluconazole capsules for only one day on D1

Primary Outcome Measures

Name	Time	Method
Proportion of subjects achieving cure at the D11±2 visit.	day 11±2	Proportion of subjects achieving cure (defined as the disappearance of VVC symptoms and signs along with a negative Candida culture) at the D11±2 visit.

Secondary Outcome Measures

Name	Time	Method
Proportion of subjects achieving clinical cure at the D11±2 visit	day 11±2	Proportion of subjects achieving clinical cure (complete disappearance of VVC symptoms and signs) at the D11±2 visit;
Proportion of subjects achieving mycological clearance at the D11±2 visit	day 11±2	Proportion of subjects achieving mycological clearance (negative growth of Candida species in fungal culture) at the D11±2 visit;
Proportion of subjects achieving clinical improvement at the D11±2 visit	day 11±2	Proportion of subjects achieving clinical improvement (partial or complete resolution of symptoms and signs, with a total VVC scale score ≤1) at the D11±2 visit
Difference in VVC scale scores between the D11±2 visit and baseline visit	day 11±2	Difference in VVC scale scores between the D11±2 visit and baseline visit
Proportion of subjects achieving cure at the D25±3 visit.	Day 25±3	Proportion of subjects achieving cure (defined as the disappearance of VVC symptoms and signs along with a negative Candida culture) at the D25±3 visit..
Proportion of subjects achieving mycological clearance at the D25±3 visit	Day 25±3	Description: Proportion of subjects achieving mycological clearance (negative growth of Candida species in fungal culture) at the D25±3 visit;
Proportion of subjects achieving clinical improvement at the D25±3 visit	Day 25±3	Description: Proportion of subjects achieving clinical improvement (partial or complete resolution of symptoms and signs, with a total VVC scale score ≤1) at the D25±3visit
Proportion of subjects requiring rescue therapy during the trial;	Day 25±3	Proportion of subjects requiring rescue therapy during the trial;
Proportion of subjects with normal vaginal microecology assessments	Day11±2 and day 25±3	Proportion of subjects with normal vaginal microecology assessments at the D11±2 and D25±3 visits
adverse events	Day 25±3	Incidence and severity of adverse events and serious adverse events
AUC0-tau	day 4	the AUC0-tau estimated using non-compartmental and/or population pharmacokinetic models
Cmax	day 4	the Cmax estimated using non-compartmental and/or population pharmacokinetic models

Trial Locations

Locations (2)

251 Yaojiayuan Road, Chaoyang District, Beijing; 🇨🇳 Beijing, Beijing, China

Beijing Obstetrics and Gynecology Hospital; 🇨🇳 Beijing, Beijing, China