| Eligibility |
Inclusion Criteria:
- 1. Women aged 40-75 (inclusive).
2. Postmenopausal women with a body mass index between 18 and 34 kg/m2, inclusive.
3. Postmenopausal, defined as 12 months of spontaneous amenorrhea or 6 months of
spontaneous amenorrhea with serum follicle-stimulating hormone levels > 40 mIU/mL or 6
weeks post-surgical bilateral oophorectomy.
4. Have moderate to severe VVA as determined by self-assessment of the following
symptoms (as none, mild, moderate, or severe), with at least 1 symptom reported as
moderate or severe: vaginal dryness; vaginal and/or vulvar irritation/itching;
dysuria; vaginal pain with sexual activity (dyspareunia); vaginal bleeding associated
with sexual activity (presence versus absence).
5. Women who currently have vaginal intercourse or other sexual activity
(masturbation, etc.) at least once a month (with or without a partner), or who had
intercourse or other sexual activity at least once a month in the past, but later
decreased sexual activity due to excessive pain or vaginal dryness. Participants must
be willing to engage in vaginal intercourse or other sexual activity (masturbation,
etc.) at least 1 time between Days 49-56 of the clinical study.
6. Participants, upon pelvic examination with speculum examination, must have a
normal-appearing vulva other than atrophic changes, normal-appearing cervix other than
atrophic changes (i.e., cervical stenosis and/or flushness with the vaginal wall) and
normal-appearing vagina (without erosions, ulcerations, scarring, or evidence of
dermatoses) other than atrophic changes (loss of ruggae, mucosal pallor, mucosal
dryness, mucosal petechiae).
7. Have an intact uterus and no prior history of endometrial ablation.
8. Vaginal cellular cytology with = 5% superficial cells.
9. Vaginal pH > 5 at Screening Visit.
10. Endometrial thickness = 4 mm on transvaginal ultrasound.
11. Current on all recommended screening and management requirements for cervical
cancer.
12. Normal mammogram report within 2 years of screening.
13. Normal manual breast examination by investigator at baseline.
14. Baseline hematology, clinical chemistry, urinalysis, prothrombin time/partial
thromboplastin time (PT/PTT) and viral serologies for human immunodeficiency virus
(HIV), hepatitis C virus (HCV), and hepatitis B surface antigen (HBsAg) all within
normal limits OR accepted by the investigator and medical monitor as not clinically
significant.
15. Normal 12-lead electrocardiogram (ECG).
16. Able to read, understand, and provide written informed consent and applicable data
protection authorization after the nature of the study has been fully explained, and
must be willing to comply with all study requirements.
17. Willing and able to correctly and independently complete all study procedures.
Exclusion Criteria:
1. A history of or physical examination finding for any significant cardiovascular,
renal, pulmonary, neurological and hepatic diseases preventing compliance with this
study.
2. A medical history of or use of anticoagulant drugs to treat or prevent coagulopathies,
thrombophilia or thromboembolic disease (deep vein thrombosis, pulmonary or systemic
embolism, stroke, or transient ischemic attack).
3. Uncontrolled hypertension (either systolic > 180 mmHg or diastolic > 105 mmHg),
treatment with Class 1 antiarrhythmics or digitalis, history of congestive heart
failure (New York Heart Association [NYHA] > Class I), or myocardial infarction within
12 months.
4. Abnormal cervical screening test within 2 years of screening. Participant can have
atypical squamous cells of undetermined significance if human papilloma
virus-negative.
5. History of or current endometrial pathology: hyperplasia, carcinoma and/or polyp
(prior history of a benign endometrial polyp with no current evidence of polyp is
acceptable).
6. A medical history of breast cancer within 5 years of screening. Participants with a
history of breast cancer more than 5 years prior to screening are considered eligible
if their disease was node-negative, nonmetastatic, and if all treatment with aromatase
inhibitors (AIs) or SERMs was completed at least 6 months prior to screening.
7. A medical history of malignant melanoma.
8. Any cancer (except nonmelanomatous skin cancer) diagnosed less than 5 years prior to
the Screening Visit.
9. A medical history of undiagnosed vaginal bleeding.
10. A known or suspected estrogen-dependent neoplasia.
11. Previous radiation treatment to the pelvis.
12. Women who have previously reported an unsatisfactory outcome from a vaginal hormone
therapy for VVA.
13. Known hypersensitivity to any ingredients in DARE-VVA1.
14. Use of vaginal hormonal products (rings, creams, gels, tablets, capsules) within 4
weeks prior to Day 1.
15. Use of transdermal estrogen or transdermal estrogen/progestin products within 4 weeks
prior to Day 1.
16. Use of oral estrogen and/or progestin therapy within 8 weeks prior to Day 1.
17. Use of intrauterine progestin therapy within 8 weeks prior to Day 1.
18. Use of progestin implants or estrogen-alone injectable drug therapy within 12 weeks
prior to Day 1.
19. Administration of estrogen pellet therapy or progestin injectable drug therapy within
6 months prior to Day 1.
20. Use of thyroid hormone replacement therapy unless the participant is on a stable dose
for > 6 months, and participant is euthyroid based on a normal, sensitive immunoassay
for thyroid-stimulating hormone (TSH).
21. Use of SERMs or AIs within 6 months prior to screening.
22. Use of anabolic or other steroids (including hormonal creams such as testosterone)
within 4 weeks prior to Day 1.
23. Use of corticosteroids, > 5 mg/day prednisone or equivalent, for more than 4 weeks
within 4 weeks prior to Day 1.
24. Participants with any self-reported active sexually transmitted disease and/or
evidence of infection (including bacterial vaginosis) on vaginal examination by the
investigator.
25. Participants with a urinary tract infection during screening as assessed by urine
dipstick test with abnormal test findings (any positive result for leukocytes AND any
positive result for nitrites).
26. Presence of clinically significant uterine fibroids.
27. Evidence of current alcohol or drug abuse in the past 60 days, including a positive
result from the urine drugs of abuse or alcohol screen, or history of drug or alcohol
dependence in the last 2 years, as assessed by the investigator. Alcohol abuse is
defined as greater than 14 standard units/week for females, and drug abuse is defined
as known psychiatric or substance abuse disorder that would interfere with
participation with the requirements of this study, including current use of any
illicit drugs. Use of medical cannabis is not exclusionary.
28. Participation in any other investigational drug or device trial in which
administration of an investigational study drug/device occurred within 30 days or
placement of a non-drug eluting medical device within 15 days prior to the Screening
Visit (Visit 1).
29. In the opinion of the investigator, participant has any disorder or finding that might
interfere with the conduct of the study.
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