A Phase 2 Study of SYM-1219 to Treat Bacterial Vaginosis
Status: | Completed |
---|---|
Conditions: | Women's Studies |
Therapuetic Areas: | Reproductive |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 12/16/2017 |
Start Date: | May 2014 |
End Date: | October 2014 |
A Phase 2, Multi-center, Prospective, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Effectiveness and Safety of SYM-1219 for the Treatment of Women With Bacterial Vaginosis
The purpose of this research study is to test the safety and effectiveness of the oral
investigational new drug, SYM-1219, for the treatment of bacterial vaginosis.
investigational new drug, SYM-1219, for the treatment of bacterial vaginosis.
Inclusion Criteria:
- Are females at least 18 years of age in good general health who are not menopausal.
- Have a clinical diagnosis of bacterial vaginosis, defined as having all of the
following criteria:
- Off-white (milky or gray), thin, homogeneous vaginal discharge
- Vaginal pH ≥ 4.7
- Presence of clue cells of ≥ 20% of the total epithelial cells on microscopic
examination of the vaginal saline wet mount
- A positive 10% KOH Whiff test.
- Have a Gram stain slide Nugent score ≥ 4 at the Baseline visit (Day 1)
Exclusion Criteria:
- Are pregnant, lactating, or planning to become pregnant during the study.
- Are suspected clinically (or confirmed diagnostically) of having alternative causes of
vaginal symptoms including candidiasis, Chlamydia trachomatis, Trichomonas vaginalis,
Neisseria gonorrhoeae or Herpes simplex.
- Have received antifungal or antimicrobial therapy (systemic or intravaginal) within 14
days prior to the Baseline visit (Day 1).
We found this trial at
16
sites
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