Study to Evaluate Equivalence of Estradiol Vaginal Cream 0.01% to Estrace® Cream 0.01% in Atrophic Vaginitis

A Randomized, Double-Blind, Placebo-Controlled, Parallel-Design, Multiple-Site Study to Evaluate the Therapeutic Equivalence of Estradiol Vaginal Cream USP, 0.01% (Teva Pharmaceuticals, USA) to Estrace® Estradiol Vaginal Cream, USP, 0.01% (Warner Chilcott) in the Treatment of Atrophic Vaginitis

The objectives of this study were to evaluate the therapeutic equivalence of the Test formulation, generic Estradiol Vaginal Cream United States Pharmacopoeia (USP), 0.01% (Teva Pharmaceuticals, United States of America) to the marketed product, Estrace® Cream estradiol vaginal cream USP, 0.01% (Warner Chilcott) in participants with atrophic vaginitis; to demonstrate the superiority of the Test and Reference (active) treatments over Placebo (vehicle) cream in participants with atrophic vaginitis; and to compare the safety of Test, Reference, and Placebo treatments in participants with atrophic vaginitis.

Study Overview

• Status: Completed
• Conditions: Atrophic Vaginitis
• Intervention / Treatment: Drug: Generic Estradiol Vaginal Cream USP, 0.01%; Drug: Estrace® Vaginal Cream USP, 0.01%; Drug: Vehicle Vaginal Cream

Detailed Description

Systemic (oral or transdermal patch administration) estrogen therapies have been shown to effectively treat symptoms of atrophic vaginitis but bear undesirable side effects including increased risk of heart attacks, stroke, endometrial cancer, and breast cancer. Topical therapies (creams and transvaginal delivery systems) provide low doses of estrogen to the vaginal mucosa to provide local relief for the symptoms of atrophic vaginitis, while reducing the unwanted side effects associated with systemic delivery systems. Low dose, topical estrogen therapy is considered most appropriate and convenient for the treatment of vaginal symptoms associated with menopause, particularly when other symptoms including bone loss or vasomotor dysfunction do not need to be targeted.

• Study Type: Interventional
• Enrollment (Actual): 663
• Phase: Phase 3

Contacts and Locations

Study Locations

• United States
  • Arizona
    • Tucson, Arizona, United States, 85710
      • Site Number 44
    • Tucson, Arizona, United States, 85712
      • Site Number 17
  • California
    • La Mesa, California, United States, 91942
      • Site Number 31
    • Sacramento, California, United States, 95821
      • Site Number 11
    • San Diego, California, United States, 91208
      • Site Number 05
    • San Diego, California, United States, 92111
      • Site Number 15
  • Colorado
    • Colorado Springs, Colorado, United States, 80923
      • Site Number 25
    • Denver, Colorado, United States, 80209
      • Site Number 01
    • Denver, Colorado, United States, 80220
      • Site Number 14
  • Connecticut
    • New London, Connecticut, United States, 06320
      • Site Number 18
  • Florida
    • Jupiter, Florida, United States, 33458
      • Site Number 06
    • Lake Worth, Florida, United States, 33461
      • Site Number 13
    • Miami, Florida, United States, 33015
      • Site Number 27
    • Miami, Florida, United States, 33130
      • Site Number 40
    • Miami, Florida, United States, 33136
      • Site Number 20
    • Miami, Florida, United States, 33144
      • Site Number 39
    • Miami, Florida, United States, 33186
      • Site Number 38
    • Miami Lakes, Florida, United States, 33014
      • Site Number 30
    • New Port Richey, Florida, United States, 34652
      • Site Number 08
    • Ormond Beach, Florida, United States, 32174
      • Site Number 03
    • Port Saint Lucie, Florida, United States, 34952
      • Site Number 45
    • Saint Petersburg, Florida, United States, 33709
      • Site Number 19
    • Sarasota, Florida, United States, 34239
      • Site Number 10
    • West Palm Beach, Florida, United States, 33409
      • Site Number 02
  • Georgia
    • Roswell, Georgia, United States, 30075
      • Site Number 29
    • Savannah, Georgia, United States, 31406
      • Site Number 22
  • Kansas
    • Wichita, Kansas, United States, 67226
      • Site Number 21
  • Louisiana
    • Metairie, Louisiana, United States, 70001
      • Site Number 33
  • Michigan
    • Kalamazoo, Michigan, United States, 49009
      • Site Number 16
    • Saginaw, Michigan, United States, 48604
      • Site Number 34
  • Nebraska
    • Lincoln, Nebraska, United States, 68510
      • Site Number 35
  • New Jersey
    • Lawrenceville, New Jersey, United States, 08648
      • Site Number 12
    • Plainsboro, New Jersey, United States, 08536
      • Site Number 26
  • North Carolina
    • Raleigh, North Carolina, United States, 27607
      • Site Number 36
    • Winston-Salem, North Carolina, United States, 27103
      • Site Number 04
    • Winston-Salem, North Carolina, United States, 27103
      • Site Number 37
  • Ohio
    • Columbus, Ohio, United States, 43213
      • Site Number 07
    • Englewood, Ohio, United States, 45322
      • Site Number 24
    • West Chester, Ohio, United States, 45069
      • Site Number 28
  • South Carolina
    • Bluffton, South Carolina, United States, 29910
      • Site Number 23
    • Mount Pleasant, South Carolina, United States, 29464
      • Site Number 41
    • Myrtle Beach, South Carolina, United States, 29572
      • Site Number 43
  • Texas
    • Dallas, Texas, United States, 75230
      • Site Number 32
  • Washington
    • Seattle, Washington, United States, 98105
      • Site Number 09

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 30 years to 75 years (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: Female

Description

Inclusion Criteria:

• Signed Informed Consent Form (ICF) that meets all criteria of current Food and Drug Administration (FDA) regulations.
• Females aged 30-75 years inclusive who are postmenopausal, defined as follows:
• At least 12 months of spontaneous amenorrhea or 6 months of spontaneous amenorrhea with serum follicle-stimulating hormone (FSH) level of >40 milli-international units per milliliter (mIU/mL); at least 6 weeks post-surgical bilateral oophorectomy, with or without hysterectomy; or hysterectomy without oophorectomy if of age that the Investigator believes would have been naturally reached 12 months of spontaneous amenorrhea.
• Vaginal pH >5.0.

• At least 1 of the following participant self-assessed moderate to severe symptoms of vulvar and vaginal atrophy (VVA) from the following list that is identified by the participant as being most bothersome to her:

  1. Vaginal Dryness
  2. Vaginal and/or vulvar irritation/itching
  3. Dysuria
  4. Vaginal pain or bleeding associated with sexual activity, provided that participant is currently sexually active and plans to remain so throughout study.
• "Normal" Screening mammogram completed within 9 months prior to Screening in all participants >40 years old.
• Normal clinical breast examination at the Screening Visit.
• 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.
• Participants with an intact uterus should have vaginal ultrasonography results to confirm an inactive endometrial lining, defined as endometrial thickness less than 4 millimeters (mm).

Exclusion Criteria:

1. Females younger than 30 years of age or older than 75 years of age.
2. Participants with a Serum follicle-stimulating hormone (FSH) level of ≤40 mIU/mL at Screening.
3. Greater than 5% superficial cells on vaginal cytology.
4. Vaginal pH ≤5.
5. Significant history or current evidence of chronic infectious disease, system disorder, organ disorder (including significant liver/kidney impairment) or other medical condition that in the Investigator's opinion would place the study participant at undue risk by participation or could jeopardize the integrity of the study evaluations.
6. Participants with an intact uterus should have vaginal ultrasonography results to confirm an inactive endometrial lining. Participants with an endometrial thickness equal to or greater than 4 mm.
7. Documented PAP smear conducted within the previous 12 months with findings that the Investigator believes would contraindicate the use of topical vaginal estradiol.

8. Participants with known concurrent vaginal infections including but not limited to:

   Candida albicans, Trichomonas vaginalis, Chlamydia trachomatis, Neisseria gonorrhea, or Gardnerella vaginalis.

9. Participants with active vaginal herpes simplex infection or have had an outbreak within 30 days of the first dosing day.
10. Participants with known, suspected, or current history of carcinoma of the breast. All participants over the age of 40 must have had a mammogram performed within 9 months of the study start and all participants will have a physical breast exam performed at Screening.
11. Participants with known, suspected or current history of hormone dependent tumor.
12. Participants with baseline systolic blood pressure of >150 millimetres of mercury (mmHg) and/or diastolic pressure >90 mmHg.
13. Any participant with undiagnosed vaginal bleeding or significant risk factors for endometrial cancer.
14. Any history of estrogen-dependent neoplasia (for example, endometrial cancer).
15. History of acute thrombophlebitis or thromboembolic disorder.
16. Any current or recent (within the previous 6 months) genital bleeding of unknown etiology.
17. Any prescription treatment or over-the-counter (OTC) or natural remedies for vaginal dryness/irritation within 28 days of Screening. Products used for lubrication during sexual intercourse within 7 days of Screening.
18. Participants whose fasting triglyceride levels are greater than 350 mg/dL.
19. Any participant with a history of radiation therapy or recent (within previous 6 weeks) surgical therapy to the vaginal or cervical areas.
20. Any known or suspected allergies that in the Investigator's opinion would compromise the safety of the participant.
21. Participants who have used vaginal hormonal products (rings, creams, gels) within the 28 days prior to Screening.
22. Any participant who has used transdermal estrogen and/or progestin therapy within the 28 days prior to Screening.
23. Participants who have used oral estrogen and/ or progestin therapy or intrauterine progestin therapy within the 56 days prior to Screening.
24. Participants who have used progestin implants or estrogen alone injectable drug therapy within the 3 months before Screening.
25. Participants who have used estrogen pellet therapy or progestin injectable drug therapy within the 6 months before Screening.
26. Participants who, in the opinion of the Investigator, would be non-compliant with the requirements of the study protocol.
27. Participants who are unable or unwilling to give informed consent.
28. Receipt of any drug as part of a research study within 30 days prior to Screening.
29. Participants who have participated in this study previously.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Quadruple

Number of Arms

3

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Generic Estradiol Vaginal Cream USP, 0.01%; Participants were to self-administer 2 grams (g) of generic Estradiol Vaginal Cream USP, 0.01% once daily at approximately the same time of the day for 7 consecutive days.	Drug: Generic Estradiol Vaginal Cream USP, 0.01%; Vaginal cream, generic formulation of the brand product.
Active Comparator: Estrace Vaginal Cream USP, 0.01%; Participants were to self-administer 2 g of Estrace Vaginal Cream USP, 0.01% once daily at approximately the same time of the day for 7 consecutive days.	Drug: Estrace® Vaginal Cream USP, 0.01%; Vaginal cream, brand product.
Placebo Comparator: Vehicle Vaginal Cream; Participants were to self-administer 2 g of vehicle vaginal cream once daily at approximately the same time of the day for 7 consecutive days.	Drug: Vehicle Vaginal Cream; Vaginal cream, placebo. Has no active ingredient

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Number of Participants Identified as a Responder After Completing Study Treatment in the Generic Estradiol Vaginal Cream and Estrace Vaginal Cream Groups	Treatment comparison of the number of participants in the PP population that were identified as responders at the end of the treatment period evaluated on Day 8 + 1 is presented. A responder was defined as a participant with at least a 25% reduction from baseline in the sum of percent basal/parabasal + percent intermediate cells on vaginal cytology and vaginal pH ≤5.0 with a change from baseline vaginal pH of at least 0.5. Any participant who withdrew from the study because of lack of efficacy was included as a non-responder.	Up to Day 9
Number of Participants Identified as a Responder After Completing Study Treatment in the Generic Estradiol Vaginal Cream, Estrace Vaginal Cream, and Vehicle Vaginal Cream Groups	Treatment comparison of the number of participants in the mITT population that were identified as responders at the end of the treatment period evaluated on Day 8 + 1 is presented. A responder was defined as a participant with at least a 25% reduction from baseline in the sum of percent basal/parabasal + percent intermediate cells on vaginal cytology and vaginal pH ≤5.0 with a change from baseline vaginal pH of at least 0.5.	Up to Day 9

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Number of Participants Identified as Treatment Success After Completing Study Treatment in the Generic Estradiol Vaginal Cream and Estrace Vaginal Cream Groups	The number of participants in the PP population that are identified as Treatment Success at the end of the treatment period evaluated on Day 8 ± 1 is presented. A Treatment Success is defined as a score of 0 or 1 at Day 8 ± 1 for the symptom identified at baseline as the most bothersome. This evaluation was based on participant self-assessed symptoms of vulvar and vaginal atrophy on a scale of 0 to 3 where 0 = none and 3 = severe. The symptoms that were evaluated were vaginal dryness, vaginal/vulvar irritation/itching, dysuria, vaginal pain associated with sexual activity, and vaginal bleeding. Any participant who withdrew from the study because of lack of efficacy was included as a non-responder.	Up to Day 9
Number of Participants Identified as Treatment Success After Completing Study Treatment in the Generic Estradiol Vaginal Cream, Estrace Vaginal Cream, and Vehicle Vaginal Cream Groups	The number of participants in the mITT Population that are identified as Treatment Success at the end of the treatment period evaluated on Day 8 ± 1 is presented. A Treatment Success is defined as a score of 0 or 1 at Day 8 ± 1 for the symptom identified at baseline as the most bothersome. This evaluation is to be based on participant self-assessed symptoms of vulvar and vaginal atrophy on a scale of 0 to 3 where 0 = none and 3 = severe. The symptoms that were evaluated were vaginal dryness, vaginal/vulvar irritation/itching, dysuria, vaginal pain associated with sexual activity, and vaginal bleeding.	Up to 9 months

Collaborators and Investigators

• Sponsor: Actavis Inc.
• Collaborators: Teva Pharmaceuticals USA
• Investigators: Study Director: Study Director, Teva Pharmaceuticals USA

Study record dates

Study Major Dates

• Study Start (Actual): May 18, 2016
• Primary Completion (Actual): February 15, 2017
• Study Completion (Actual): February 15, 2017

Study Registration Dates

• First Submitted: September 20, 2017
• First Submitted That Met QC Criteria: September 25, 2017
• First Posted (Actual): September 27, 2017

Study Record Updates

• Last Update Posted (Actual): December 26, 2019
• Last Update Submitted That Met QC Criteria: December 11, 2019
• Last Verified: December 1, 2019

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Pathological Conditions, Anatomical; Vaginal Diseases; Vaginitis; Atrophic Vaginitis; Atrophy; Physiological Effects of Drugs; Hormones; Hormones, Hormone Substitutes, and Hormone Antagonists; Estrogens; Contraceptive Agents, Hormonal; Contraceptive Agents; Reproductive Control Agents; Contraceptive Agents, Female; Estradiol; Estradiol 17 beta-cypionate; Estradiol 3-benzoate; Polyestradiol phosphate
• Other Study ID Numbers: 71436001

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: No

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: Yes
• Studies a U.S. FDA-regulated device product: No