MedPath

Estradiol

Generic Name
Estradiol
Brand Names
Activella 1/0.5 28 Day, Activelle, Amabelz 0.5/0.1 28 Day, Angeliq 0.25/0.5 28 Day, Bijuva, Climara, Climara Pro, Combipatch, Divigel, Dotti, Elestrin, Estalis, Estrace, Estradot, Estring, Estrogel, Etyqa 0.5/0.1 28 Day, Evamist, Imvexxy 4 Mcg Starter Pack, Lopreeza 1/0.5 28 Day, Lyllana, Menostar, Mimvey, Minivelle, Myfembree, Oesclim, Oriahnn 28 Day Kit, Prefest 30 Day, Vagifem, Vivelle, Yuvafem
Drug Type
Small Molecule
Chemical Formula
C18H24O2
CAS Number
50-28-2
Unique Ingredient Identifier
4TI98Z838E
Background

Estradiol is a naturally occurring hormone circulating endogenously in females. It is commercially available in several hormone therapy products for managing conditions associated with reduced estrogen, such as vulvovaginal atrophy and hot flashes. Some available forms of estradiol include oral tablets, injections, vaginal rings, transdermal patches, sprays, gels, and creams.

When used for oral or IM administration, estradiol is commonly synthesized as a pro-drug ester (such as Estradiol acetate, Estradiol benzoate, Estradiol cypionate, Estradiol dienanthate, and Estradiol valerate). Because it has a low oral bioavailability on its own, estradiol is commonly formulated with an ester side-chain. Ethinylestradiol (EE) is a synthetic form of estradiol commonly used as the estrogenic component of most combination oral contraceptive pills (OCPs). Ethinyl estradiol is different from estradiol due to its higher biovailability and increased resistance to metabolism, rendering it more suitable for oral administration.

Indication

Estradiol is indicated in various preparations for the treatment of moderate to severe vasomotor symptoms and vulvar and vaginal atrophy due to menopause, for the treatment of hypoestrogenism due to hypogonadism, castration, or primary ovarian failure, and for the prevention of postmenopausal osteoporosis. It is also used for the treatment of breast cancer (only for palliation therapy) in certain men or women with metastatic disease, and for the treatment of androgen-dependent prostate cancer (only for palliation therapy). It is also used in combination with other hormones as a component of oral contraceptive pills for preventing pregnancy (most commonly as Ethinylestradiol, a synthetic form of estradiol).

A note on duration of treatment

Recommendations for treatment of menopausal symptoms changed drastically following the release of results and early termination of the Women's Health Initiative (WHI) studies in 2002 as concerns were raised regarding estrogen use. Specifically, the combined estrogen–progestin group was discontinued after about 5 years of follow up due to a statistically significant increase in invasive breast cancer and in cardiovascular events.

Following extensive critique of the WHI results, Hormone Replacement Therapy (HRT) is now recommended to be used only for a short period (for 3-5 years postmenopause) in low doses, and in women without a history of breast cancer or increased risk of cardiovascular or thromboembolic disease. Estrogen for postmenopausal symptoms should always be given with a progestin component due to estrogen's stimulatory effects on the endometrium; in women with an intact uterus, unopposed estrogen has been shown to promote the growth of the endometrium which can lead to endometrial hyperplasia and possibly cancer over the long-term.

Associated Conditions
Atrophic Vaginitis, Breast Cancer, Breast engorgement caused by Postpartum state, Heavy Menstrual Bleeding, Hypogonadism female, Kraurosis Vulvae, Metastatic Breast Cancer, Osteoporosis, Postmenopausal Osteoporosis, Premature Ovarian Failure (POF), Prostate Cancer, Severe Pain, Urogenital atrophy, Vasomotor Symptoms Associated With Menopause, Vulvo Vaginal Atrophy, Advanced androgen dependent Prostate cancer, Female castration, Hypoestrogenism
Associated Therapies
Contraception, Hormone Replacement Therapy, Palliative Treatment

A Study To Estimate The Effect of PF-06650833 On The Pharmacokinetics (PK) of Oral Contraceptive (OC)

Phase 1
Completed
Conditions
Healthy
Interventions
First Posted Date
2021-10-01
Last Posted Date
2023-10-02
Lead Sponsor
Pfizer
Target Recruit Count
10
Registration Number
NCT05064332
Locations
🇺🇸

Qps-Mra, Llc, South Miami, Florida, United States

Contraceptive Hormone and Reward Measurement (CHARM Study)

Phase 4
Recruiting
Conditions
Mood
Hedonic Function
Neural Activity
Oral Hormonal Contraceptive Use
Interventions
First Posted Date
2021-09-28
Last Posted Date
2024-11-04
Lead Sponsor
University of Colorado, Denver
Target Recruit Count
144
Registration Number
NCT05058872
Locations
🇺🇸

University of Colorado Denver Anschutz Medical Campus, Aurora, Colorado, United States

Estradiol and Progesterone Levels Following Frozen Embryo Transfer

Phase 4
Completed
Conditions
Infertility
Interventions
First Posted Date
2021-08-09
Last Posted Date
2025-01-03
Lead Sponsor
Copenhagen University Hospital at Herlev
Target Recruit Count
305
Registration Number
NCT04997525
Locations
🇩🇰

Herlev University Hospital, Herlev, Denmark

Study of Relugolix Alone and Relugolix Combined With Hormonal Add-Back Therapy in Healthy Premenopausal Female Participants

Phase 1
Completed
Conditions
Healthy
Interventions
First Posted Date
2021-07-27
Last Posted Date
2021-07-27
Lead Sponsor
Myovant Sciences GmbH
Target Recruit Count
48
Registration Number
NCT04978688
Locations
🇺🇸

Clinical Study Site, Minneapolis, Minnesota, United States

Tamoxifen Versus Estradiol for Unscheduled Bleeding in Etonogestrel Implant Users, a Randomized Pilot Trial

Phase 4
Withdrawn
Conditions
Vaginal Bleeding
Interventions
First Posted Date
2021-06-21
Last Posted Date
2022-06-03
Lead Sponsor
Virginia Commonwealth University
Registration Number
NCT04933240
Locations
🇺🇸

Virginia Commonwealth University, Richmond, Virginia, United States

🇺🇸

Shanthi Ramesh, Richmond, Virginia, United States

Estradiol and Progesterone in Hospitalized COVID-19 Patients

Phase 2
Terminated
Conditions
Covid19
Interventions
First Posted Date
2021-04-29
Last Posted Date
2023-06-27
Lead Sponsor
Tulane University
Target Recruit Count
10
Registration Number
NCT04865029
Locations
🇺🇸

Tulane University Medical Center, New Orleans, Louisiana, United States

Oestrogen Treatment for COVID-19 Symptoms

Phase 2
Conditions
COVID-19
Interventions
First Posted Date
2021-04-21
Last Posted Date
2021-04-21
Lead Sponsor
Hamad Medical Corporation
Target Recruit Count
2000
Registration Number
NCT04853069
Locations
🇶🇦

Hamad Medical Corporation, Doha, Qatar

Estrogen Administration for the Treatment of NASH in Postmenopausal Women

Phase 3
Recruiting
Conditions
NASH - Nonalcoholic Steatohepatitis
Interventions
First Posted Date
2021-04-06
Last Posted Date
2024-08-01
Lead Sponsor
Massachusetts General Hospital
Target Recruit Count
60
Registration Number
NCT04833140
Locations
🇺🇸

Massachusetts General Hospital, Boston, Massachusetts, United States

Gonadotropin Releasing Hormone Agonist (GnRHa) Versus Estrogen and Progesterone for Luteal Support in High Responders

Phase 4
Conditions
Pregnancy Early
Miscarriage
Ovarian Hyperstimulation Syndrome
Interventions
First Posted Date
2021-03-15
Last Posted Date
2021-04-01
Lead Sponsor
Assaf-Harofeh Medical Center
Target Recruit Count
100
Registration Number
NCT04797338
Locations
🇮🇱

Shamir Medical center, Be'er Ya'aqov, Israel

Pre-Exposure Prophylaxis (PrEP)- Gender Affirming Hormone Therapy (GAHT) Interactions in TGW

First Posted Date
2021-02-18
Last Posted Date
2025-05-22
Lead Sponsor
Johns Hopkins University
Target Recruit Count
20
Registration Number
NCT04760691
Locations
🇺🇸

Johns Hopkins School of Medicine Drug Development Unit, Baltimore, Maryland, United States

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