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

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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.


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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Saginaw, MI
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Birmingham, AL
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Clearwater, FL
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Detroit, MI
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Houston, TX
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Jackson, TN
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LawrenceVille, New Jersey 08648
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LawrenceVille, NJ
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New Bern, NC
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North Miami, FL
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Philadelphia, PA
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Plainsboro, NJ
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Roswell, GA
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San Antonio, TX
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San Diego, CA
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Seattle, WA
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Virginia Beach, VA
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