Study to Evaluate the Equivalence of Estradiol Vaginal Cream to Reference Standard in the Treatment of Vaginal Atrophy

NCT ID: NCT03332303

Last Updated: 2024-05-30

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE3
• Total Enrollment: 540 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2017-10-26
• Study Completion Date: 2018-03-15

Brief Summary

The objectives of this study are to evaluate the therapeutic equivalence of the Test formulation, Estradiol Vaginal Cream 0.01% (Prasco, LLC) to the marketed product, Estrace® Cream (estradiol vaginal cream, 0.01%) in patients with vulvar and vaginal atrophy, and compare the safety of Test, Reference and Placebo treatments in patients with vulvar and vaginal atrophy.

Conditions

Vulvar and Vaginal Atrophy

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

Experimental: Estradiol Vaginal Cream, USP, 0.01% (Prasco LLC)

Estradiol Vaginal Cream, USP, 0.01%, administered once daily for 7 days.

Intervention: Drug: Estradiol Vaginal Cream, USP, 0.01%

Group Type: EXPERIMENTAL

Estradiol Vaginal Cream

Intervention Type: DRUG

Estradiol Vaginal Cream

Active Comparator: Estrace® Cream

Estrace® Cream (Estradiol Vaginal Cream, USP, 0.01%), administered once daily for 7 days.

Intervention: Drug: Estrace® Cream (Estradiol Vaginal Cream, USP, 0.01%)

Group Type: ACTIVE_COMPARATOR

Estrace® Cream

Intervention Type: DRUG

Estrace® Cream

Placebo Comparator: Placebo (Test vehicle cream) Vaginal Cream

Placebo (Test vehicle cream) Vaginal Cream, administered once daily for 7 days.

Intervention: Drug: Placebo (Test vehicle cream) Vaginal Cream

Group Type: PLACEBO_COMPARATOR

Vehicle Cream

Intervention Type: DRUG

Vehicle Cream

Interventions

Estrace® Cream

Estrace® Cream

Intervention Type: DRUG

Estradiol Vaginal Cream

Estradiol Vaginal Cream

Intervention Type: DRUG

Vehicle Cream

Vehicle Cream

Intervention Type: DRUG

Other Intervention Names

Estradiol Vaginal Cream; Placebo

Eligibility Criteria

Inclusion Criteria

1. Signed IRB-approved informed consent form that meets all criteria of current FDA regulations.

2. Postmenopausal females aged 30-75 years inclusive. Postmenopausal is defined as follows:

1. At least 6 months of spontaneous amenorrhea.

2. At least 6 weeks post-surgical bilateral oophorectomy, with or without hysterectomy.

3. Hysterectomy without oophorectomy if of age that the Investigator believes would have naturally reached 12 months of spontaneous amenorrhea if uterus had remained intact.

3. Patients with a serum Follicle Stimulating Hormone (FSH) level of ≥ 40 mIU/mL at Screening.

4. Have ≤ 5% superficial cells on vaginal smear cytology.

5. Have a vaginal pH > 5.0.

6. At least one of the following patient self-assessed moderate to severe symptoms of VVA from the following list that is identified by the patient as being the most bothersome to her:

• Vaginal Dryness
• Vaginal and/or Vulvar Irritation/Itching
• Dysuria
• Vaginal Pain associated with sexual activity
• Vaginal Bleeding associated with sexual activity (presence or absence)

• Provided that patient is currently sexually active and plans to remain so throughout the study.

7. Have "Normal" Screening mammogram completed within 9 months before Screening in all patients > 40 years old, with no findings that, in the opinion of the Investigator, would indicate any suspicion of breast malignancy.

8. Normal clinical breast examination at Screening.

9. Patients with an intact uterus (including patients who underwent a partial hysterectomy) must have a documented papanicolaou (PAP) smear conducted within the previous 12 months with no findings that the Investigator believes would contraindicate the use of topical vaginal estradiol.

10. Patients with an intact uterus should have vaginal ultrasonography results within 3 months before Screening to confirm an inactive endometrial lining, defined as endometrial thickness < 4 mm.

Exclusion Criteria

1. Significant history or current evidence of chronic infectious disease, system disorder, organ disorder or other medical condition that in the Investigator's opinion would place the study patient at undue risk by participation or could jeopardize the integrity of the study evaluations.

2. Any clinically significant laboratory finding that, in the Investigator's opinion would contraindicate the use of estradiol or compromise patient safety.

3. Patients with known concurrent vaginal infections including but not limited to: Candida albicans, Trichomonas vaginalis, Chlamydia trachomatis, Neisseria gonorrhea or Gardnerella vaginalis.

4. Patients with active vaginal herpes simplex infection or have had an outbreak within 30 days before the Screening.

5. Patients with known, suspected or current history of carcinoma of the breast.

6. Patients with baseline systolic blood pressure of > 150 mmHg and/or diastolic pressure > 90 mmHg.

7. Any patient with past or current undiagnosed vaginal bleeding or significant risk factors for endometrial cancer.

8. Any history of estrogen-dependent neoplasia (e.g., endometrial cancer).

9. Patients with known, suspected or current history of hormone dependent tumor.

10. History of acute thrombophlebitis or thromboembolic disorder.

11. Any prescription treatment for vaginal dryness/irritation within 14 days before Screening or any over-the-counter or natural remedies within 7 days before Screening.

12. Any prescription treatment for bacterial or yeast infections within 30 days before Screening.

13. Fasting triglyceride levels > 350 mg/dL.

14. History of radiation therapy or recent (within previous 6 weeks) surgical therapy to the vaginal or cervical areas.

15. Any known or suspected allergies that, in the Investigator's opinion, would compromise the safety of the patient.

16. Patients who have used vaginal hormonal products (rings, creams, gels) within the 7 days before Screening.

17. Patients who have used transdermal estrogen and/or progestin therapy within the 28 days before Screening.

18. Patients who have used oral estrogen and/or progestin therapy or intrauterine progestin therapy within the 56 days before Screening.

19. Patients who have used progestin implants or estrogen alone injectable drug therapy within the 3 month before Screening.

20. Patients who have used estrogen pellet therapy or progestin injectable drug therapy within 6 months before Screening.

21. History of significant alcohol abuse within 1 year prior to Screening or regular use of alcohol within 6 months before Screening (more than 14 units of alcohol per week [1 unit = 150 mL of wine, 360 mL of beer, or 45 mL of 40% alcohol]).

22. History of significant drug abuse within 1 year prior to Screening, use of soft drugs (such as marijuana) within 3 months before Screening, or hard drugs (such as cocaine, phencyclidine [PCP], crack, opioid derivatives including heroin, and amphetamine derivatives) within 1 year before Screening.

23. Use within 30 days of Screening with known strong CYP3A4 inducers or inhibitors that, in the opinion of the Investigator, may affect estrogen metabolism. Examples of strong CYP3A4 inhibitors are macrolide antibiotics such as clarithromycin and telithromycin; azole antifungals such as itraconazole and ketoconazole; antidepressants such as nefazodone; and foods such as grapefruit or grapefruit juice. Examples of strong CYP3A4 inducers are anticonvulsants such as carbamazepine and phenytoin; bactericidals such as rifampin and rifabutin; and natural health products such as St. John's wort.

24. Inability to understand the requirements of the study and the relative information or are unable or not willing to comply with the study protocol.

25. Receipt of any drug as part of a research study within 30 days before Screening.

26. Employees of the Investigator or research center or their immediate family members.

27. Patients who have participated in this study previously.

• Minimum Eligible Age: 30 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: No

Sponsors

Prasco LLC

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Gail Gongas

Role: STUDY_DIRECTOR

Novum

Locations

Douglas Young, MD

Sacramento, California, United States

Medical Center for Clinical Research

San Diego, California, United States

Women's Health Care Research Corp.

San Diego, California, United States

Downtown Women's Health Care

Denver, Colorado, United States

Avail Clinical Research, LLC

DeLand, Florida, United States

Health Awareness, Inc.

Jupiter, Florida, United States

New Age Medical Research Corporation

Miami, Florida, United States

Panax Clinical Research

Miami Lakes, Florida, United States

Suncoast Clinical Research

New Port Richey, Florida, United States

Ormond Medical Arts Pharmaceutical Research Center

Ormond Beach, Florida, United States

Health Awareness, Inc.

Port Saint Lucie, Florida, United States

Physician Care Clinical Research, LLC

Sarasota, Florida, United States

Well Pharma Medical Research Group

South Miami, Florida, United States

Meridien Research, Inc.

St. Petersburg, Florida, United States

Comprehensive Clinical Trials, LLC

West Palm Beach, Florida, United States

Cypress Medical Research Center, LLC

Wichita, Kansas, United States

Praetorian Pharmaceutical

Marrero, Louisiana, United States

Southern Clinical Research Associates

Metairie, Louisiana, United States

Canton Obstetrics and Gynecology

Canton, Michigan, United States

Beyer Research

Kalamazoo, Michigan, United States

Women's Clinic of Lincoln

Lincoln, Nebraska, United States

Lawrence Ob-Gyn Clinical Research, LLC

Lawrenceville, New Jersey, United States

Aventiv Research, Inc.

Columbus, Ohio, United States

Novum PRS

Pittsburgh, Pennsylvania, United States

Coastal Carolina Research Center

Mt. Pleasant, South Carolina, United States

Vernon & Waldrep OBGYN Associates

Dallas, Texas, United States

Women's Clinical Research Center dba Seattle Women's Health, Research, Gynecology

Seattle, Washington, United States

Countries

United States

Provided Documents

Document Type: Study Protocol

View Document

Document Type: Statistical Analysis Plan

View Document

Other Identifiers

71759501

Identifier Type: -

Identifier Source: org_study_id