Approval Probability
TA Base Rate
Adjusted LOA
ML Risk
Label indication Lopreeza is indicated for: Lopreeza is an estrogen and progestin combination indicated in a woman with a uterus for: Treatment of Moderate to Severe Vasomotor Symptoms due to Menopause (1.1) Treatment of Moderate to Severe Symptoms of Vulvar and Vaginal Atrophy due to Menopause (1.2) Limitations of Use : When prescribing solely for the treatment of moderate to severe symptoms of vulvar and vaginal atrophy due to… FDA label
Also known as 17B-estradiol, Estrace, 17β-estradiol
Estradiol · 4 trials · 4 indications
Determine the differences in vaginal cytokines: interleukin (IL)-1β and IL-8 between premenopausal and postmenopausal women.
• Change from Baseline to Week 12 in the percentage of vaginal superficial cells (by vaginal cytologic smear) compared to placebo
• Change from Baseline to Week 12 in the percentage of vaginal parabasal cells (by vaginal cytologic smear) compared to placebo
• Change from Baseline to Week 12 in vaginal pH as compared to placebo
• 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
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.
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).
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.
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.
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.
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).
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).
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).
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).
| Arm | Type | Description |
|---|---|---|
| 1.Premenopausal women | NO_INTERVENTION | No treatment |
| 2.Postmenopausal women with hormones | EXPERIMENTAL | Oral 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 Capsule | EXPERIMENTAL | Estradiol 4mcg Vaginal Softgel Capsule |
| Estradiol 10mcg Vaginal Softgel Capsule | EXPERIMENTAL | Estradiol 10mcg Vaginal Softgel Capsule |
| Estradiol 25mcg Vaginal Softgel Capsule | EXPERIMENTAL | Estradiol 25mcg Vaginal Softgel Capsule |
| Placebo Vaginal Softgel Capsule | PLACEBO_COMPARATOR | Placebo Vaginal Softgel Capsule |
| Treatment 1 | EXPERIMENTAL | Combined Estradiol 1 mg / Progesterone 100 mg softgel capsule formulation and placebo taken orally once a day for twelve months. |
| Treatment 2 | EXPERIMENTAL | Combined Estradiol 0.5 mg / Progesterone 100 mg softgel capsule formulation and placebo taken orally once a day for twelve months. |
| Treatment 3 | EXPERIMENTAL | Combined Estradiol 0.5 mg / Progesterone 50 mg softgel capsule formulation and placebo, taken orally once a day for twelve months. |
| Treatment 4 | EXPERIMENTAL | Combined Estradiol 0.25 mg / Progesterone 50 mg softgel capsule formulation and placebo, taken orally once a day for twelve months. |
| Placebo | PLACEBO_COMPARATOR | Two Placebo softgel capsules taken orally once a day for twelve months. |
| Name | Type | Description |
|---|---|---|
| oral estradiol 1.0 mg | DRUG | one tablet of oral estradiol 1.0 mg once a day for 28 days |
| oral progesterone 100 mg | DRUG | one tablet of oral progesterone 100 mg once a day for 14 days |
| Estradiol | DRUG | - |
| Placebo | DRUG | - |
| Progesterone | DRUG | - |
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...
Estradiol is a small molecule estrogen therapy being developed by TherapeuticsMD for menopause and vulvovaginal atrophy. It is studied for symptoms that include vulvar and vaginal atrophy, dyspareunia, and painful intercourse in postmenopausal women. The clinical program includes Phase 3 trials in the United States and Canada.
Estradiol targets ESR1, the estrogen receptor alpha, and acts as an agonist. Binding to this receptor activates estrogen signaling, which underlies its use in menopausal and vulvovaginal atrophy indications. ESR1 agonism is the mechanism described for this small molecule in the TherapeuticsMD program.
Estradiol in this program is developed by TherapeuticsMD, Inc., which trades under the ticker TXMD. The company is running the clinical development of oral and vaginal estradiol formulations for menopause and vulvovaginal atrophy. TherapeuticsMD is the sponsor listed for the trials in this program.
Estradiol is in Phase 3 development for menopause and vulvovaginal atrophy. The program includes completed Phase 3 trials as well as an earlier Phase 2 study. It is an investigational therapy in clinical development, and the available program information does not indicate FDA approval.
The estradiol program includes NCT02253173, a completed Phase 3 trial of vaginal softgel capsules in postmenopausal women with vulvar and vaginal atrophy, and NCT01942668, a completed Phase 3 safety and efficacy study of estradiol combined with progesterone for vasomotor symptoms. Other completed studies include NCT02449902 and NCT02224313.