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Estradiol

Phase 3

Menopause | Small molecule | Endocrine |TherapeuticsMD, Inc.|Last Updated: Mar 19, 2020

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Market & Valuation
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Trial Design
RandomizedDouble-BlindPLACEBO_CONTROLLEDDMCBiomarker
Total Trials3
Total Enrollment1,915
FDA Designations
No designations recorded
Clinical trial landscape

Estradiol · 4 trials · 4 indications

Phase 3 3Phase 2 1
NCT02224313Effect of Oral Estradiol and Progesterone Therapy on Vaginal Cytokines in Postmenopausal WomenMenopause
COMPLETED20 Analytics
NCT02253173Estradiol Vaginal Softgel Capsules in Treating Symptoms of Vulvar and Vaginal Atrophy in Postmenopausal WomenVulvovaginal Atrophy
COMPLETED764 Analytics
NCT01942668A Safety and Efficacy Study of the Combination Estradiol and Progesterone to Treat Vasomotor SymptomsMenopause
COMPLETED1,845 Analytics
PHASE3COMPLETED
Effect of Oral Estradiol and Progesterone Therapy on Vaginal Cytokines in Postmenopausal Women
MenopauseUnlock trial analytics
PHASE3COMPLETED
Estradiol Vaginal Softgel Capsules in Treating Symptoms of Vulvar and Vaginal Atrophy in Postmenopausal Women
Vulvovaginal AtrophyUnlock trial analytics
PHASE3COMPLETED
A Safety and Efficacy Study of the Combination Estradiol and Progesterone to Treat Vasomotor Symptoms
MenopauseUnlock trial analytics
Study Endpoints
Primary Endpoints
Vaginal Cytokines at Baseline
At baseline visit

Determine the differences in vaginal cytokines: interleukin (IL)-1β and IL-8 between premenopausal and postmenopausal women.

Co-Primary Efficacy Endpoint - Vaginal Superficial Cells
Baseline and 12 Weeks

• Change from Baseline to Week 12 in the percentage of vaginal superficial cells (by vaginal cytologic smear) compared to placebo

Co-Primary Efficacy Endpoint - Vaginal Parabasal Cells
Baseline and 12 Weeks

• Change from Baseline to Week 12 in the percentage of vaginal parabasal cells (by vaginal cytologic smear) compared to placebo

Co-Primary Efficacy Endpoint - Vaginal pH
Baseline and 12 Weeks

• Change from Baseline to Week 12 in vaginal pH as compared to placebo

Co-Primary Efficacy Endpoint - Severity of Most Bothersome Symptom (Dyspareunia)
Baseline and Week 12

• Change from Baseline to Week 12 on the severity of the MBS of dyspareunia (vaginal pain associated with sexual activity) associated with VVA as compared to placebo VVA Symptoms Self-Assessment Questionnaire Severity Scale: 0 = None, 1 = Mild, 2 = Moderate, 3 = Severe. Subjects assessed severity at Baseline and Week 12

Co-Primary Efficacy Endpoint: Frequency of Moderate to Severe Vasomotor Symptoms (MITT-VMS)
Baseline and Week 4

Mean change in frequency of moderate to severe vasomotor symptoms from Baseline to Week 4. The baseline was the most recent 7 consecutive days of data prior to randomization. The weekly frequency of moderate to severe hot flushes was calculated from the daily diary record using a forward counting process of 7 day intervals beginning with the baseline date. Weekly frequency equals total number of moderate to severe hot flushes for the subject week.

Co-Primary Efficacy Endpoint: Severity of Moderate to Severe Vasomotor Symptoms (MITT-VMS)
Baseline and Week 4

Mean change in severity of moderate to severe vasomotor symptoms at Baseline to mild, moderate to severe vasomotor symptoms at Week 4. The baseline was the most recent 7 consecutive days of data prior to randomization. The severity score was derived as follows: mild = 1, moderate = 2, severe = 3. Baseline Weekly Severity Score = (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of moderate to severe hot flushes over 7 days). On Treatment Weekly Severity Score = \[(number of mild hot flushes for 7 days) x 1 + (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of mild, moderate and severe hot flushes over 7 days).

Primary Safety Endpoint: Endometrial Protection - Hyperplasia
Baseline and Month 12

Endometrial biopsies centrally evaluated by 2 primary pathologists using criteria from Blaustein's Pathology text. Pathologists classified bx into 1 of following 3 categories: Cat.1: Non-endometrial malignancy/non-hyperplasia; Cat.2: Endometrial hyperplasia; Cat.3: Endometrial malignancy. Consensus reached when 2 primary pathologist agreed on any of above categories; if primary pathologists disagreed on presence of hyperplasia, result of 3rd pathologist was utilized and final decision regarding presence of hyperplasia was based on diagnosis of majority. If all 3 reads disparate, final diagnosis based on most severe dx. Incidence rate calculated as: I=A/B where I=incidence rate at M12 evaluation, A=all new subjects with biopsies positive for endometrial hyperplasia during study but post-Baseline, B=all subjects w/biopsies following M11 meeting criteria specified plus all subjects w/biopsies positive for endometrial hyperplasia by any pathologists before M11.

Analysis of Change From Baseline to Day 15 in Maturation Index of the Vaginal Cell Type (Parabasal Cells)
Baseline to 15 days post-treatment
Analysis of Change From Baseline to Day 15 in Maturation Index of the Vaginal Cell Type (Superficial Cells)
Baseline to 15 days post-treatment
Analysis of Change From Baseline to Day 15 in Maturation Index of the Vaginal Cell Type (Intermediate Cells)
Baseline to 15 days post-treatment
Analysis of Change From Baseline to Day 15 in Vaginal pH
Baseline to 15 days post-treatment
Analysis of Change From Baseline to Day 15 in Severity of the Most Bothersome Vulvar and Vaginal Atrophy (VVA) Symptom
Baseline to 15 days post-treatment

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.

Analysis of Change From Baseline to Day 15 in Vaginal Bleeding Associated With Sexual Activity
Baseline to 15 days post-treatment

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.

Analysis of Change From Baseline to Day 15 in Investigator Assessment of the Vaginal Mucosa (Assessment of Vaginal Color)
Baseline to 15 days post-treatment

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).

Analysis of Change From Baseline to Day 15 in Investigator Assessment of the Vaginal Mucosa (Assessment of Vaginal Epithelial Integrity)
Baseline to 15 days post-treatment

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).

Change From Baseline to Day 15 in Investigator Assessment of the Vaginal Mucosa (Assessment of Vaginal Epithelial Surface Thickness)
Baseline to 15 days post-treatment

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).

Analysis of Change From Baseline to Day 15 in Investigator Assessment of the Vaginal Mucosa (Assessment of Vaginal Secretions)
Baseline to 15 days post-treatment

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).

Secondary Endpoints
Vaginal Cytokines During Follow-up
At 14 days and 28 days follow-up
Secondary Efficacy Endpoints - Vaginal Superficial Cells
Baseline and Week 2
Secondary Efficacy Endpoints- Vaginal Superficial Cells
Baseline and Week 6
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Study Design & Arms
AllocationNON_RANDOMIZED
MaskingQUADRUPLE
ModelPARALLEL
PurposeBASIC_SCIENCE
Treatment Arms
ArmTypeDescription
1.Premenopausal womenNO_INTERVENTIONNo treatment
2.Postmenopausal women with hormonesEXPERIMENTALOral hormone therapy will be given to women in this group. Daily dose of oral "estradiol" 1 mg will be given the first 14 days after enrollment. Then a daily dose of oral "estradiol" 1 mg and "progesterone" 100 mg for 14 days will be given during the following 14 days.
Estradiol 4mcg Vaginal Softgel CapsuleEXPERIMENTALEstradiol 4mcg Vaginal Softgel Capsule
Estradiol 10mcg Vaginal Softgel CapsuleEXPERIMENTALEstradiol 10mcg Vaginal Softgel Capsule
Estradiol 25mcg Vaginal Softgel CapsuleEXPERIMENTALEstradiol 25mcg Vaginal Softgel Capsule
Placebo Vaginal Softgel CapsulePLACEBO_COMPARATORPlacebo Vaginal Softgel Capsule
Treatment 1EXPERIMENTALCombined Estradiol 1 mg / Progesterone 100 mg softgel capsule formulation and placebo taken orally once a day for twelve months.
Treatment 2EXPERIMENTALCombined Estradiol 0.5 mg / Progesterone 100 mg softgel capsule formulation and placebo taken orally once a day for twelve months.
Treatment 3EXPERIMENTALCombined Estradiol 0.5 mg / Progesterone 50 mg softgel capsule formulation and placebo, taken orally once a day for twelve months.
Treatment 4EXPERIMENTALCombined Estradiol 0.25 mg / Progesterone 50 mg softgel capsule formulation and placebo, taken orally once a day for twelve months.
PlaceboPLACEBO_COMPARATORTwo Placebo softgel capsules taken orally once a day for twelve months.
Interventions
NameTypeDescription
oral estradiol 1.0 mgDRUGone tablet of oral estradiol 1.0 mg once a day for 28 days
oral progesterone 100 mgDRUGone tablet of oral progesterone 100 mg once a day for 14 days
EstradiolDRUG -
PlaceboDRUG -
ProgesteroneDRUG -
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Eligibility Criteria
Age Range20 Years to 65 Years
SexFEMALE
Healthy VolunteersYes
Study Sites1

Inclusion Criteria: * Premenopausal and Postmenopausal women: 1. Female between the ages of 20 and 40 years (premenopausal arm), OR be a female between the ages of 45 and 65 years (postmenopausal arm) willing to participate in the study, as documented by signing the informed consent form. 2. P...

Countries:United StatesCanada
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