Medroxyprogesterone acetate

Generic Name
Medroxyprogesterone acetate
Brand Names
Depo-provera, Depo-subq Provera, Premphase 28 Day, Prempro 0.625/2.5 28 Day, Provera
Drug Type
Small Molecule
Chemical Formula
C24H34O4
CAS Number
71-58-9
Unique Ingredient Identifier
C2QI4IOI2G
Background

Medroxyprogesterone acetate (MPA) is a progesterone derivative that is more resistant to metabolism for improved pharmacokinetic properties. MPA can be use to treat secondary amenorrhea, endometrial hyperplasia, abnormal uterine bleeding, osteoporosis, vasomotor symptoms in menopause, vulvar and vaginal atrophy, prevent pregnancy, manage pain in endometriosi...

Indication

Medroxyprogesterone acetate (MPA) oral tablets are indicated to treat secondary amenorrhea, reduce the incidence of endometrial hyperplasia in postmenopausal women, and to treat abnormal uterine bleeding due to hormonal imbalance, not organic pathology. Oral tablets containing MPA and conjugated estrogens are indicated to prevent postmenopausal osteoporosis ...

Associated Conditions
Abnormal Uterine Bleeding, Amenorrhea, Endometrial Hyperplasia, Endometriosis related pain, Metastatic Renal Cell Carcinoma ( mRCC), Osteoporosis, Pain, Postmenopausal Osteoporosis, Pregnancy, Vasomotor Symptoms Associated With Menopause, Vulvo Vaginal Atrophy, Metastatic Endometrial carcinoma
Associated Therapies
Contraception, Estrogen Replacement Therapy, Hormonal Contraception therapy

PK of Depo SubQ Injected in the Upper Arm

Not Applicable
Completed
Conditions
Interventions
First Posted Date
2010-06-14
Last Posted Date
2013-08-19
Lead Sponsor
FHI 360
Target Recruit Count
26
Registration Number
NCT01143207
Locations
🇺🇸

Clinical Research Center, Dept. of Obstetrics & Gynegology, Eastern Virginia Medical School, Norfolk, Virginia, United States

Study of Self or Clinic Administration of DepoProvera

Not Applicable
Completed
Conditions
Interventions
First Posted Date
2009-11-25
Last Posted Date
2019-05-07
Lead Sponsor
Carolyn L. Westhoff
Target Recruit Count
132
Registration Number
NCT01019369
Locations
🇺🇸

Columbia University/New York Presbyterian Hospital, New York, New York, United States

Treatment of Hot Flushes Caused by Leuprorelin 11.25 mg in Prostate Adenocarcinoma

First Posted Date
2009-11-11
Last Posted Date
2015-07-30
Lead Sponsor
Takeda
Target Recruit Count
311
Registration Number
NCT01011751
Locations
🇫🇷

Professor Jacques IRANI, Poitiers, France

Medroxyprogesterone Acetate Injection 150 mg/1 mL in Postmenopausal Women

Phase 1
Completed
Conditions
Interventions
First Posted Date
2009-01-27
Last Posted Date
2024-08-19
Lead Sponsor
Teva Pharmaceuticals USA
Target Recruit Count
124
Registration Number
NCT00830414
Locations
🇩🇪

AAI Deutschland GmbH & Co. KG, Neu-Ulm, Germany

Treatment of Non-Gestational Acute Uterine Bleeding: A Randomized Trial

Not Applicable
Completed
Conditions
First Posted Date
2006-07-10
Last Posted Date
2015-03-11
Lead Sponsor
Kaiser Permanente
Target Recruit Count
240
Registration Number
NCT00350480
Locations
🇺🇸

Kaiser Permanente Sunset, Los Angeles, California, United States

Study of Hot Flashes and Night Sweats in Postmenopausal Women Receiving Combination Raloxifene and Oral Estrogen

Phase 2
Completed
Conditions
First Posted Date
2006-06-01
Last Posted Date
2007-05-15
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
150
Registration Number
NCT00332553
Locations
🇺🇸

For additional information regarding investigative sites for this trial, contact 1-877- CTLILLY (1-877-285-4559, 1-317-615-4559) Mon-Fri from 9AM to 5PM Eastern Time (UTC/GMT-5 hours, EST), or speak with your personal physician., Indianapolis, Indiana, United States

Cytokines in Patients With Metastatic Renal Cell Carcinoma of Intermediate Prognosis

Phase 3
Completed
Conditions
First Posted Date
2006-02-14
Last Posted Date
2006-02-16
Lead Sponsor
Centre Leon Berard
Target Recruit Count
456
Registration Number
NCT00291369
Locations
🇫🇷

Centre Leon Berard, Lyon, France

Somatropin Treatment to Final Height in Turner Syndrome

First Posted Date
2005-09-19
Last Posted Date
2010-01-27
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
154
Registration Number
NCT00191113
Locations
🇨🇦

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri 9 am - 5 pm Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Sherbrooke, Quebec, Canada

Estrogen, HDL, and Coronary Heart Disease in Women

First Posted Date
2004-06-04
Last Posted Date
2016-04-21
Lead Sponsor
Tufts University
Target Recruit Count
309
Registration Number
NCT00083824
Locations
🇺🇸

HNRCA at Tufts University, Boston, Massachusetts, United States

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