VG101 Phase I/II to Treat Vulvar and Vaginal Atrophy in Post-Menopausal Women

Status unconfirmed · Phase 1/Phase 2

Conditions studied: Vaginal Atrophy, Vulvar Atrophy

In brief

To conduct a prospective, randomized, blinded, placebo controlled, dose escalation clinical trial in 4 cohorts of 10 postmenopausal women (total N=40) aged 45 to 65 years with at least one menopausal vaginal symptom, vaginal pH \> 5.0 and \> 20% parabasal vaginal epithelial cells.

Key facts

Study ID

NCT00453089

Run by

Bionovo

People needed

40

Starts

2012-06-01

Expected to finish

2013-08-01

Last updated by the study team

2012-02-08

Who can join

Age: 45 and older, up to 65. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• Women between the ages of 45 and 65
• Postmenopausal documented by: (a) at least one year of amenorrhea; (b) 6- 12 months of amenorrhea with serum FSH > 40 IU/ml; (c) 6 weeks post-surgical bilateral oophorectomy with or without hysterectomy, or (d) hysterectomy with serum FSH levels > 40 IU/ml.
• Self-report at least one moderate to severe symptom of vulvar or vaginal atrophy from the following list:
• Vaginal dryness (none, mild, moderate or severe)
• Vaginal and/or vulvar discomfort (none, mild, moderate, severe)
• Vaginal and/or vulvar irritation (none, mild, moderate, severe)
• Vaginal itching (none, mild, moderate, severe)
• Vaginal pain associated with sexual activity (none, mild, moderate or severe)
• < 5% superficial cells on vaginal cytologic smear.
• Vaginal pH >5.0
• Willing to use an intravaginal cream containing Chinese herbs for the treatment of vaginal symptoms.
• Provide informed consent.

You may not qualify if…

• History of breast, uterine or ovarian cancer or melanoma.
• Abnormal mammogram or breast examination within the last 9 months suggestive of cancer.
• Abnormal Pap smear or pelvic examination within the last 9 months suggestive of cancer.
• Any uterine or vaginal bleeding within the six months prior to enrollment (except following the screening Pap smear).
• Double-wall endometrial thickness that exceeds 5 mm measured on transvaginal ultrasound.
• Pregnant or lactating.
• Use of any vaginal moisturizer (Replens, KY Silk-E, Astroglide Silken Secret, Senselle) within 30 days of screening.
• Use of any oral, transdermal, vaginal, or systemic estrogen or estrogen/progestin product within 30 days of screening.
• Use of raloxifene, tamoxifen or aromatase inhibitors within 12 weeks of screening.
• Current urinary tract infection (dipstick urinalysis positive for leukocyte estrace, nitrates or blood)
• History of cardiovascular disease.
• History of venous thromboembolic disease.
• Use of another investigational agent within 12 weeks of screening.
• Any medical or psychiatric condition that, in the investigator's opinion, would preclude the participant from completing questionnaires or measures, adhering to the protocol or completing the trial, including limited English literacy, severe illness, plans to move, substance abuse, significant psychiatric problems, or dementia.
• No access to a telephone

Where it is running

• University of Alabama, Birmingham — Birmingham, Alabama, United States
• University of California, San Francisco — San Francisco, California, United States

Full record on ClinicalTrials.gov

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