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Assessment of efficacy and safety of Lipid based Amphotericin B gel 0.1% (Amfy gel®) in patients with moderate to severe vulvovaginal candidiasis

Phase 4
Completed
Conditions
Health Condition 1: B373- Candidiasis of vulva and vagina
Registration Number
CTRI/2014/02/004409
Lead Sponsor
Intas Pharmaceuticals Ltd
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
60
Inclusion Criteria

1.Female patientsâ?? >=18 years of age, on an acceptable form of birth control throughout treatment period.

2.The patient willing to give written, signed and dated informed consent to participate in the study before initiating any study related procedure.

3.Clinical diagnosis of symptomatic vulvovaginal candidiasis (score at screening and baseline visit >=7 â?? moderately severe cases) confirmed at screening visit by positive KOH wet mount test.

4.History of completing a single standard dose or short course of treatment with anti-fungal azoles within three months of the current symptomatic episode of VVC.

5.Patient complies with all clinical trial instructions and procedures.

Exclusion Criteria

1.Pregnant or breastfeeding or planning to become pregnant during the treatment period.

2.Diagnosed with disseminated candidiasis or requires systemic antifungal therapy.

3.Has received any topical/systemic antifungal therapy within 7 days prior to visit 2 (baseline).

4.Women suffering from other active infectious cause(s) of vulvovaginitis (e.g., Bacterial vaginosis, Trichomonasvaginalis, Chlamydia trachomatis, Neisseria gonorrhea, symptomatic Herpes Simplex Virus-1 (HSV-1), symptomatic HSV-2, or symptomatic human papilloma virus).

5.Women with current use of any immunosuppressive drugs, including systemic or topical vaginal corticosteroids.

6.Known case of Hypersensitivity or intolerance (e.g., elevation of liver enzymes) to Amphotericin B.

7.Diagnosed with any concomitant condition that, in the opinion of the investigator, could interfere with the evaluation of efficacy or safety, or would make it unlikely that the patient would complete the study.

Study & Design

Study Type
PMS
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Proportion of patients with clinical cureTimepoint: At the end of 14 day course of treatment.
Secondary Outcome Measures
NameTimeMethod
â?¢Any adverse event reported voluntarily, observed or enquired during the safety period <br/ ><br>â?¢Proportion of patients with negative KOH wet mount test at the end of 14 day course of treatment. <br/ ><br>Timepoint: Throughout study drug administration period <br/ ><br>(14 days) <br/ ><br>At the end of 14 day course of treatment <br/ ><br>
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