Medroxyprogesterone Acetate

drug
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Also known as Adgyn medroAmenClimanorCurretabCycrinDepo-progeveraDepo-proveraDepo-provera oncologyDepo-subq provera 104Depot-medroxyprogesterone acetateFarlutalFarlutal 100Farlutal 200Farlutal 250Farlutal 500Farlutal inyectableG03AC06MedroxiprogesteronaMedroxyprogesterone

Summary

Medroxyprogesterone Acetate (CHEMBL717) is an approved small-molecule female contraceptive drug (ATC L02AB02); indicated across 34 conditions including endometriosis and neoplasm.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Small molecule
  • ATC class: L02AB02 (+2 more)
  • Indications: 34 conditions
  • Clinical trials: 73
  • Chemistry: 386.5 Da · C24H34O4

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL717
NameMedroxyprogesterone Acetate
TypeSmall molecule
Max phase4
FDA approvedyes
PubChem CID6279
ChEBICHEBI:6716
ATCL02AB02, G03AC06, G03DA02
Molecular formulaC24H34O4
Molecular weight386.5
InChIKeyPSGAAPLEWMOORI-PEINSRQWSA-N

SMILES: C[C@H]1C[C@@H]2[C@H](CC[C@]3([C@H]2CC[C@@]3(C(=O)C)OC(=O)C)C)[C@@]4(C1=CC(=O)CC4)C

IUPAC name: [(6S,8R,9S,10R,13S,14S,17R)-17-acetyl-6,10,13-trimethyl-3-oxo-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-17-yl] acetate

ChEBI definition: An acetate ester resulting from the formal condensation of the 17α-hydroxy group of medroxyprogesterone with the carboxy group of acetic acid. A widely used progestin in menopausal hormone therapy and in progestogen-only birth control.

Pharmacological roles (ChEBI): progestin, androgen, female contraceptive drug, synthetic oral contraceptive, adjuvant, inhibitor, antioxidant, antineoplastic agent.

Also known as: Adgyn medro, Amen, Climanor, Curretab, Cycrin, Depo-progevera, Depo-provera, Depo-provera oncology, Depo-subq provera 104, Depot-medroxyprogesterone acetate, Farlutal, Farlutal 100

Patent coverage: 13,467 distinct patent families (51,452 SureChEMBL compound mentions), from 1 matched compound structure(s). Mentions count patents naming the compound (not distinct inventions), so promiscuous / reference molecules inflate the mention figure — families are the dedup metric.

Targets

Targets

Broader ChEMBL bioactivity targets: 22 (assay-derived). Sample: Prelamin-A/C, ATP-binding cassette sub-family C member 4, Androgen receptor, Histamine H2 receptor, Mineralocorticoid receptor, Glucocorticoid receptor, Progesterone receptor, Estrogen receptor, Muscarinic acetylcholine receptor M2, Muscarinic acetylcholine receptor M1.

Bioactivity

ChEMBL activities: 74 potent at pChembl ≥ 5 of 86 total. Top 30 by potency (10 = 0.1 nM, 6 = 1 µM):

TargetpChemblTypeValueUnitActivity ID
PGR10EC500.1nMCHEMBL_ACT_299910
PGR9.92EC500.12nMCHEMBL_ACT_299913
PGR9.92EC500.12nMCHEMBL_ACT_417776
PGR9.82EC500.15nMCHEMBL_ACT_1211170
PGR9.82EC500.15nMCHEMBL_ACT_228557
PGR9.82EC500.15nMCHEMBL_ACT_48433
PGR9.82EC500.15nMCHEMBL_ACT_619048
PGR9.82EC500.15nMCHEMBL_ACT_695331
PGR9.82EC500.15nMCHEMBL_ACT_828769
PGR9.48EC500.33nMCHEMBL_ACT_228562
PGR9.48EC500.33nMCHEMBL_ACT_48435
PGR9.47Ki0.34nMCHEMBL_ACT_1211173
PGR9.47Ki0.34nMCHEMBL_ACT_1734223
PGR9.47Ki0.34nMCHEMBL_ACT_228558
PGR9.47Ki0.34nMCHEMBL_ACT_48436
PGR9.47Ki0.34nMCHEMBL_ACT_619051
PGR9.47Ki0.34nMCHEMBL_ACT_695333
PGR9.47Ki0.34nMCHEMBL_ACT_828772
PGR9.4EC500.4nMCHEMBL_ACT_2448993
PGR9.3EC500.5nMCHEMBL_ACT_1278208
PGR9.3EC500.5nMCHEMBL_ACT_2448978
PGR9.3EC500.5nMCHEMBL_ACT_369874
AR9Kd1nMCHEMBL_ACT_24824131
PGR8.85Ki1.4nMCHEMBL_ACT_2449034
AR8.54Ki2.9nMCHEMBL_ACT_1211182
AR8.54Ki2.9nMCHEMBL_ACT_228559
AR8.54Ki2.9nMCHEMBL_ACT_48437
AR8.54Ki2.9nMCHEMBL_ACT_619052
AR8.54Ki2.9nMCHEMBL_ACT_828773
PGR8.52AC503nMCHEMBL_ACT_25204426

Target pathways

No target-pathway data for this drug (no mapped target genes).

Indications & clinical

Indications

34 indications (6 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).

IndicationTrial phaseMONDOEFO
endometriosis4MONDO:0005133EFO:0001065
neoplasm4MONDO:0005070EFO:0000616
renal cell carcinoma4MONDO:0005086EFO:0000681
hyperplasia4MONDO:0005043EFO:0000536
renal carcinoma4MONDO:0005206EFO:0002890
infertility disorder3MONDO:0005047EFO:0000545
prostate adenocarcinoma3MONDO:0005082EFO:0000673
coronary artery disorder3MONDO:0005010EFO:0001645
heart disorder3MONDO:0005267EFO:0003777
osteoporosis3MONDO:0005298EFO:0003882
diabetes mellitus3MONDO:0005015EFO:0000400
hypertensive disorder3MONDO:0005044EFO:0000537
myocardial ischemia3MONDO:0024644EFO:1001375
thrombotic disease3MONDO:0000831MONDO:0000831
kidney cancer3MONDO:0002367MONDO:0002367
endometrium neoplasm3MONDO:0021251MONDO:0011962
Turner syndrome3MONDO:0019499MONDO:0019499
systemic lupus erythematosus3MONDO:0007915MONDO:0007915
cardiovascular disorder3MONDO:0004995EFO:0000319
bone disorder3MONDO:0005381EFO:0004260
sleep apnea syndrome2MONDO:0005296EFO:0003877
HIV infectious disease2MONDO:0005109EFO:0000180
primary ovarian failure2MONDO:0005387HP:0008209
Alzheimer disease2MONDO:0004975MONDO:0004975
breast neoplasm2MONDO:0021100MONDO:0007254

9 further indication records had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.

Clinical trials

Total trials: 73.

Phase distribution

PhaseTrials
PHASE319
Not specified15
PHASE214
PHASE411
PHASE17
PHASE2/PHASE35
EARLY_PHASE12

Top trials by phase / activity

NCTPhaseStatusTitle
NCT06637189PHASE4NOT_YET_RECRUITINGProtocol with Progestin-primed Ovarian Stimulation (PPOS) from the Beginning of Stimulation Versus Protocol with GnRH Antagonists for Ovarian Stimulation in Patients Undergoing DUOSTIM with Embryo Accumulation for PGT-A.
NCT01074892PHASE4COMPLETEDA Study Comparing Mirena and Systemic Progestin for Endometrial Hyperplasia
NCT01148420PHASE4COMPLETEDDMPA & High Dose Oral Progestin (MPA) Tablets in Outpatient Treatment of Acute Excessive Vaginal Bleeding
NCT01776203PHASE4TERMINATEDStudy of a Progestin to Prevent Bleeding Associated With Initiation of Medical Menopause With GnRH Agonist
NCT01822288PHASE4COMPLETEDThe Impact of Hormone Therapy on Lower Urinary Tract Symptoms, Sexual Function and Psychosomatic Disorder
NCT02340013PHASE4COMPLETEDEndometrial Shedding Prior to Ovulation Induction Pilot Study
NCT02872818PHASE4COMPLETEDApoptotic Signaling Pathways in Rats With Endometrial Hyperplasia
NCT03034057PHASE4COMPLETEDSayana Press UK Self-Injection Study
NCT03309176PHASE4COMPLETEDStair Step Study
NCT04654741PHASE4UNKNOWNThe Rate of Embryo Euploidy in Progestin-primed Ovarian Stimulation Cycles
NCT05651282PHASE4COMPLETEDRisk Evaluation and Screening to Tailor Prevention and Reduce the Incidence of Endometrial Cancer
NCT05255653PHASE2/PHASE3RECRUITINGRefining Adjuvant Treatment IN Endometrial Cancer Based On Molecular Features
NCT06904274PHASE3RECRUITINGMirena for the Treatment of Nonatypical Endometrial Hyperplasia for 6 Months
NCT07124195PHASE3NOT_YET_RECRUITINGNanocrystalline Megestrol for Managing Chemotherapy-Induced Nausea and Vomiting
NCT07319429PHASE2/PHASE3RECRUITINGRefining Fertility-sparing Treatment in Endometrial Carcinoma Based on Molecular Classification
NCT00000419PHASE3TERMINATEDSafety of Estrogens in Lupus: Hormone Replacement Therapy
NCT00000466PHASE3COMPLETEDPostmenopausal Estrogen/Progestin Interventions (PEPI)
NCT00000559PHASE3COMPLETEDWomen’s Estrogen/Progestin Lipid Lowering Hormone Atherosclerosis Regression Trial (WELL-HART)
NCT00000605PHASE3COMPLETEDEstrogen and Graft Atherosclerosis Research Trial (EAGER)
NCT00002920PHASE3COMPLETEDS9630, Medroxyprogesterone in Treating Women With Breast Cancer
NCT00004650PHASE3COMPLETEDPhase III Randomized Study of the Effect of Postmenopausal Estrogen Replacement Therapy on Alveolar Bone Loss
NCT00026286PHASE3COMPLETEDHormone Replacement Therapy for Hot Flashes and/or Vaginal Symptoms in Postmenopausal Women Receiving Tamoxifen for Breast Cancer
NCT00030914PHASE3COMPLETEDMedroxyprogesterone Compared With Venlafaxine in Treating Hot Flashes in Women
NCT00066157PHASE2/PHASE3COMPLETEDAlzheimer’s Disease: Therapeutic Potential of Estrogen
NCT00083824PHASE2/PHASE3COMPLETEDEstrogen, HDL, and Coronary Heart Disease in Women
NCT00191113PHASE3COMPLETEDSomatropin Treatment to Final Height in Turner Syndrome
NCT00291369PHASE3COMPLETEDCytokines in Patients With Metastatic Renal Cell Carcinoma of Intermediate Prognosis
NCT00360490PHASE3COMPLETEDStudy in Women With Idiopathic Menorrhagia to Determine the Reduction in Menstrual Blood Loss (MBL) After Treatment With the Levonorgestrel-releasing Intrauterine System (IUS)
NCT00416429PHASE3COMPLETEDMedroxyprogesterone or Interferon and/or Aldesleukin in Treating Patients With Metastatic Kidney Cancer
NCT01011751PHASE3COMPLETEDTreatment of Hot Flushes Caused by Leuprorelin 11.25 mg in Prostate Adenocarcinoma
NCT01472315PHASE2/PHASE3COMPLETEDPostmenopausal Women,Treatment of Sleep Apnea and Co-morbidities
NCT02103764PHASE3UNKNOWNEfficacy of Cyclic DSG Compared With Cyclic MPA for the Treatment of Anovulatory DUB
NCT02943655PHASE3COMPLETEDTreatment of Heavy and/or Prolonged Menstrual Bleeding Without Organic Cause
NCT03300960PHASE3COMPLETEDUsefulness of Medroxyprogesterone Acetate in Follicular Phase in Oocyte Donors. Undergoing Ovarian Stimulation
NCT03675139PHASE3COMPLETEDMPA Versus Dydrogesterone for Management of Endometrial Hyperplasia Without Atypia
NCT05247268PHASE2RECRUITINGGonadotropin-releasing Hormone Agonist (GnRHa) Plus Letrozole In Young Women With Early Endometrial Cancer
NCT05675787PHASE2RECRUITINGMedroxyprogesterone Acetate Plus Atorvastatin in Young Women With Early Endometrial Carcinoma and Atypical Endometrial Hyperplasia
NCT06979596PHASE2RECRUITINGA Study of MK-5684 in People With Certain Solid Tumors (MK-5684-015/OMAHA-015)
NCT00003179PHASE2TERMINATEDSurgery Plus Medroxyprogesterone in Preventing Endometrial Cancer
NCT00033358PHASE2COMPLETEDHormone Therapy in Preventing Endometrial Cancer in Patients With a Genetic Risk For Hereditary Nonpolyposis Colon Cancer

Clinical evidence (CIViC)

No CIViC predictive evidence (expected for non-precision-medicine drugs).

Pharmacology

Pharmacogenomics

No PharmGKB pharmacogenomic data curated for this drug.

No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).