TXV13-01 Estradiol Vaginal Softgel Capsules in Treating Postmenopausal Women With Symptoms of Vulvar and Vaginal Atrophy

Menopause Clinical Trial

Official title:

A Phase 1, Randomized, Double-blind, Placebo-Controlled Study to Evaluate the Safety and Efficacy of TX-12-004-HR in Postmenopausal Women With Symptoms of Vulvar and Vaginal Atrophy (VVA)

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02449902
• Other study ID #: TXV13-01
• Status: Completed
• Phase: Phase 2
• First received: May 18, 2015
• Last updated: November 5, 2015
• Start date: July 2013
• Est. completion date: September 2013

Study information

• Verified date: November 2015
• Source: TherapeuticsMD
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

The study was designed to evaluate the efficacy and safety of TX-12-004-HR 10 μg in treating moderate to severe symptoms of vaginal atrophy associated with menopause after 14 days of treatment, and to estimate the effect size and variability of vulvovaginal atrophy endpoints. In addition, the systemic exposure to estradiol from single and multiple doses of TX-12-004-HR was to be investigated.

Description:

This study was a randomized, double-blind, placebo-controlled trial to evaluate safety and efficacy of the TX-12-004-HR formulation in reducing moderate to severe symptoms of vaginal atrophy associated with menopause and to investigate the systemic exposure to estradiol following once daily intravaginal administrations of TX-12-004-HR for 14 days.

Postmenopausal subjects who met the study entry criteria were randomized to one of two treatment groups (TX-12-004-HR or Placebo). During the Screening period subjects were asked to self-assess the symptoms of vulvar and/or vaginal atrophy, including vaginal dryness, vaginal and/or vulvar irritation/itching, dysuria, vaginal pain associated with sexual activity and vaginal bleeding associated with sexual activity. Subjects with at least one self-assessed moderate to severe symptom of vulvar and/or vaginal atrophy identified by the subject as being most bothersome to her were eligible to participate in the study.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 50
• Est. completion date: September 2013
• Est. primary completion date: September 2013
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 40 Years to 75 Years

Eligibility

Inclusion Criteria:

1. Be a female between 40 and 75 years (at the time of randomization) who is willing to participate in the study, as documented by signing the informed consent form.

2. Be a postmenopausal woman. Postmenopausal is defined with at least 12 months of spontaneous amenorrhea or 12 months post bilateral oophorectomy, with or without hysterectomy (documented by an operative report or patient reported). Women = 60 years of age who have had a hysterectomy without bilateral oophorectomy prior to natural menopause are considered menopausal.

3. Have a baseline evaluation requirements:

• =5% superficial cells on vaginal smear cytology

• Vaginal pH > 5.0

• Estradiol level = 50 pg/ml

• At least one self-assessed moderate to severe symptom of vulvar and/or vaginal atrophy from the following list that is identified by the subject as being most bothersome to her:

• Vaginal dryness

• Vaginal pain associated with sexual activity

• Vaginal and/or vulvar irritation/itching

• Dysuria

• Vaginal bleeding associated with sexual activity (absence vs. presence)

4. Have a Body Mass Index (BMI) less than or equal to 34 kg/m2. (BMI values should be rounded to the nearest integer [e.g., 34.4 rounds down to 34, while 26.5 rounds up to 27]).

5. Be willing to abstain from using products (other than study medication) that contain estrogen throughout study participation.

6. Be judged by the Principal Investigator or Sub-investigator as being in otherwise generally good health based on a pre-study medical evaluation performed within 28 days prior to the initial dose of study medication. The medical evaluation findings must include:

• a normal or non-clinically significant physical examination, including vital signs (sitting blood pressure, heart rate, respiratory rate and temperature).

• a normal or non-clinically significant pelvic examination.

• a mammogram that shows no sign of significant disease (can be performed within previous 9 months prior to initial dose of study medication). An acceptable mammogram is defined as a mammogram in which no masses or other findings are identified that is suspicious of malignancy. The site must obtain a copy of the official report for the subject's study file, and it must be verified that the mammogram itself is available if needed for additional assessment.

• a normal or non-clinically significant clinical breast examination. An acceptable breast examination is defined as no masses or other findings identified that are suspicious of malignancy.

• a normal Screening Papanicolaou ("Pap") smear (ASCUS with high risk- human papillomavirus (HPV) negative is acceptable).

• within normal limits or non-clinically significant laboratory evaluation results

• sitting systolic blood pressure =140 mmHg and diastolic blood pressure =90 mmHg at Screening. A subject may be taking up to two antihypertensive medications.

7. Be willing to abstain from sexual activity and use of vaginal douching within 24 hours prior to screening and Visit 3 vaginal pH measurements.

Exclusion Criteria:

1. Be currently hospitalized.

2. Have a history of thrombosis of deep veins or arteries or a thromboembolic disorder.

3. Have a history of coronary artery or cerebrovascular disease.

4. Have a history of liver or kidney dysfunction/disorder.

5. Have a history of gallbladder dysfunction/disorders (e.g., cholangitis, cholecystitis), unless gallbladder has been removed.

6. Have a history of diabetes, thyroid disease (subjects with diet-controlled diabetes, or controlled hypothyroid disease at Screening are not excluded), or any other endocrinological disease.

7. Have a history of estrogen-dependent neoplasia.

8. Have a history of atypical ductal hyperplasia of the breast.

9. Have a history of undiagnosed vaginal bleeding.

10. Have a vaginal infection requiring treatment

11. Have any history of endometrial hyperplasia or uterine/endometrial, breast or ovarian cancer.

12. Have any history of other malignancy within the last 5 years, with the exception of basal cell (excluded if within 1 year) or non-invasive squamous cell (excluded if within 1 year) carcinoma of the skin.

13. Have a history of any other cardiovascular, hepatic, renal, pulmonary, hematologic, gastrointestinal, endocrine, immunologic, dermatologic, neurologic, psychological, or musculoskeletal disease or disorder that is clinically significant in the opinion of the Principal Investigator or Medical Sub-Investigator.

14. Have contraindication to estrogen therapy or allergy to the use of estradiol or any components of the investigational drugs.

15. Use 15 or more cigarettes per day.

16. Have a history of drug and/or alcohol abuse within one year of start of study.

17. Have used, within 28 days prior to Screening, or plan to use during the study, any prescription or over-the-counter (OTC) medications (including herbal products) that would be expected to interact with estradiol therapy.

18. Use of any type of vaginal preparation (including lubricants and moisturizers) within 14 days prior to Screening.

19. Have used estrogen alone or estrogen/progestin for any of the following time periods:

• Vaginal hormonal products (rings, creams, gels) within 3 months prior to Screening.

• Transdermal estrogen alone or estrogen/progestin products within 8 weeks prior to Screening.

• Oral estrogen and/or progestin therapy within 8 weeks prior to Screening.

• Progestational implants, estrogen or estrogen/progestational injectable drug therapy within 3 months prior to Screening.

• Estrogen pellet therapy or progestational injectable drug therapy within 6 months prior to Screening.

• Percutaneous estrogen lotions/gels within 8 weeks prior to Screening.

• Oral, topical, vaginal, patch, implantable or injectable androgen therapy within 8 weeks prior to Screening.

20. Have any reason which, in the opinion of the Principal Investigator or Medical Sub-Investigator, would prevent the subject from safely participating in the study or complying with protocol requirements.

21. Have contraindication to any planned study procedure (e.g., blood collection).

22. Have participated in another clinical trial within 30 days prior to screening, have received an investigational drug within the three months prior to the initial dose of study medication, or be likely to participate in a clinical trial or receive another investigational medication during the study.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Atrophy
• Dyspareunia
• Menopause
• Painful Intercourse
• Vulvovaginal Atrophy

Intervention

Drug:
• Estradiol
1 10 µg capsule inserted vaginally for 14 days.
• placebo
1 placebo capsule inserted vaginally for 14 days.

Locations

Country	Name	City	State
United States	Avail Clinical Research	DeLand	Florida

Sponsors (1)

Lead Sponsor	Collaborator
TherapeuticsMD

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Analysis of Change From Baseline to Day 15 in Maturation Index of the Vaginal Cell Type (Parabasal Cells)		Baseline to 15 days post-treatment	No
Primary	Analysis of Change From Baseline to Day 15 in Maturation Index of the Vaginal Cell Type (Superficial Cells)		Baseline to 15 days post-treatment	No
Primary	Analysis of Change From Baseline to Day 15 in Maturation Index of the Vaginal Cell Type (Intermediate Cells)		Baseline to 15 days post-treatment	No
Primary	Analysis of Change From Baseline to Day 15 in Vaginal pH		Baseline to 15 days post-treatment	No
Primary	Analysis of Change From Baseline to Day 15 in Severity of the Most Bothersome Vulvar and Vaginal Atrophy (VVA) Symptom	The severity of the most bothersome VVA symptom was self-assessed by each subject using a VVA questionnaire. The questionnaire has a 4-point scoring scale with: None=0, Mild=1, Moderate=2, and Severe=3. The lower the score, the least bothersome it is to the subject.	Baseline to 15 days post-treatment	No
Primary	Analysis of Change From Baseline to Day 15 in Vaginal Bleeding Associated With Sexual Activity	Total number (N=10) of participants analyzed within each treatment group who were sexually active at both Baseline and Day 15 and provided a response at both visits.	Baseline to 15 days post-treatment	No
Primary	Analysis of Change From Baseline to Day 15 in Investigator Assessment of the Vaginal Mucosa (Assessment of Vaginal Color)	Outcome was measured by using a severity scale. No Atrophy is pink in color (0). Mild atrophy is lighter in color (1). Moderate atrophy is pale in color (2). Severe atrophy is transparent, either no color or inflamed (3).	Baseline to 15 days post-treatment	No
Primary	Analysis of Change From Baseline to Day 15 in Investigator Assessment of the Vaginal Mucosa (Assessment of Vaginal Epithelial Integrity)	Outcome was measured by using a severity scale. No Atrophy=normal(0). Mild atrophy=vaginal surface bleeds with scraping(1). Moderate atrophy=vaginal surface bleeds with light contact(2). Severe atrophy=vaginal surface has petechiae before contact and bleeds with light contact(3).	Baseline to 15 days post-treatment	No
Primary	Change From Baseline to Day 15 in Investigator Assessment of the Vaginal Mucosa (Assessment of Vaginal Epithelial Surface Thickness)	Outcome was measured by using a severity scale. No Atrophy has rogation and elasticity of vault(0). Mild atrophy has poor rogation with some elasticity noted of vaginal vault(1). Moderate atrophy is smooth, some elasticity of vaginal vault(2). Severe atrophy is smooth, no elasticity, constriction of the upper one third of vagina or loss of vaginal tone (cystocele and rectocele)(3).	Baseline to 15 days post-treatment	No
Primary	Analysis of Change From Baseline to Day 15 in Investigator Assessment of the Vaginal Mucosa (Assessment of Vaginal Secretions)	Outcome was measured by using a severity scale. No Atrophy has normal clear secretions noted on vaginal walls(0). Mild atrophy has superficial coating of secretions, difficulty with speculum insertion(1). Moderate atrophy is scant not covering the entire vaginal vault, may need lubrication with speculum insertion to prevent pain(2). Severe atrophy has none, inflamed, ulceration noted, need lubrication with speculum insertion to prevent pain(3).	Baseline to 15 days post-treatment	No