Desogestrel

drug
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Also known as AizeaCerazetteCerelleDesogestrel component of bekyreeDesogestrel component of cyclessaDesogestrel component of desogenDesogestrel component of enskyceDesogestrel component of isibloomDesogestrel component of karivaDesogestrel component of mircetteDesogestrel component of ortho-ceptDesogestrel component of pimtreaDesogestrel component of velivetDesogestrel component of vioreleDesogestrel component of volneaDesomonoFeanollaMircetteNacrez

Summary

Desogestrel (CHEMBL1533) is an approved small-molecule contraceptive drug (ATC G03AC09); indicated across 5 conditions including polycystic ovary syndrome and amenorrhea.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Small molecule
  • ATC class: G03AC09
  • Indications: 5 conditions
  • Clinical trials: 21
  • Chemistry: 310.5 Da · C22H30O

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL1533
NameDesogestrel
TypeSmall molecule
Max phase4
FDA approvedno
PubChem CID40973
ChEBICHEBI:4453
ATCG03AC09
Molecular formulaC22H30O
Molecular weight310.5
InChIKeyRPLCPCMSCLEKRS-BPIQYHPVSA-N

SMILES: CC[C@]12CC(=C)[C@H]3[C@H]([C@@H]1CC[C@]2(C#C)O)CCC4=CCCC[C@H]34

IUPAC name: (8S,9S,10R,13S,14S,17R)-13-ethyl-17-ethynyl-11-methylidene-1,2,3,6,7,8,9,10,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-17-ol

Pharmacological roles (ChEBI): contraceptive drug, progestin, synthetic oral contraceptive.

Also known as: Aizea, Cerazette, Cerelle, Desogestrel, Desogestrel component of bekyree, Desogestrel component of cyclessa, Desogestrel component of desogen, Desogestrel component of enskyce, Desogestrel component of isibloom, Desogestrel component of kariva, Desogestrel component of mircette, Desogestrel component of ortho-cept

Patent coverage: 2,612 distinct patent families (9,566 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: 20 (assay-derived). Sample: Androgen receptor, Glucocorticoid receptor, D(1A) dopamine receptor, Estrogen receptor, Progesterone receptor, Muscarinic acetylcholine receptor M2, Prostaglandin G/H synthase 1, Sodium-dependent noradrenaline transporter, Type-1 angiotensin II receptor, Sodium-dependent serotonin transporter.

Bioactivity

ChEMBL activities: 15 potent at pChembl ≥ 5 of 25 total. Top 30 by potency (10 = 0.1 nM, 6 = 1 µM):

TargetpChemblTypeValueUnitActivity ID
PGR8.52AC503nMCHEMBL_ACT_25204359
PGR8.52AC503nMCHEMBL_ACT_25222976
P152076.96AC50110nMCHEMBL_ACT_25232823
AR6.92AC50120nMCHEMBL_ACT_25203426
NR3C16.85AC50140nMCHEMBL_ACT_25175774
SHBG6.6Kd251.2nMCHEMBL_ACT_2155691
ESR16.25AC50560nMCHEMBL_ACT_25138926
CHRM25.74AC501830nMCHEMBL_ACT_25195804
SLC6A25.72AC501890nMCHEMBL_ACT_25146068
NR1I25.62AC502400nMCHEMBL_ACT_25188121
ESR15.54AC502900nMCHEMBL_ACT_25167244
SLC6A25.29AC505100nMCHEMBL_ACT_25144920
DRD35.29AC505100nMCHEMBL_ACT_25194590
ADORA35.22AC506000nMCHEMBL_ACT_25134129
SLC6A45AC5010000nMCHEMBL_ACT_25150256

Target pathways

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

Indications & clinical

Indications

5 indications (0 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
polycystic ovary syndrome3MONDO:0008487EFO:0000660
amenorrhea3MONDO:0001836EFO:0010269
infertility disorder3MONDO:0005047EFO:0000545
central sleep apnea syndrome2MONDO:0004731MONDO:0800026

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

Clinical trials

Total trials: 21.

Phase distribution

PhaseTrials
PHASE45
Not specified5
PHASE14
PHASE23
PHASE32
PHASE2/PHASE32

Top trials by phase / activity

NCTPhaseStatusTitle
NCT06334315PHASE4RECRUITINGOral Contraceptive Pill (OCP) Pharmacogenomics
NCT01738724PHASE4TERMINATEDStudy of the Efficacy of Dienogest in the Treatment of Uterine Leiomyomas When Compared to Desogestrel and Goserelin
NCT02757287PHASE4WITHDRAWNDesogestrel (DSG) and Corifollitropin(FSH-CTP) Alfa for Ovarian Stimulation in Donors
NCT04728659PHASE4UNKNOWNDesogestrel Versus GnRH Antagonist in IVF/ICSI
NCT05002738PHASE4COMPLETEDDesogestrel-containing COCP Pharmacokinetic Validation Study
NCT00946192PHASE3COMPLETEDFat Mediated Modulation of Reproductive and Endocrine Function in Young Athletes
NCT01243697PHASE2/PHASE3COMPLETEDAssessment of Desogestrel in Ondine Syndrome
NCT02103764PHASE3UNKNOWNEfficacy of Cyclic DSG Compared With Cyclic MPA for the Treatment of Anovulatory DUB
NCT04941833PHASE2/PHASE3COMPLETEDDesogestrel for the Preoperative Treatment of Endometrioma Compared With Placebo
NCT00563472PHASE2COMPLETEDFeasibility Study Into the Contraceptive Effect of Estetrol
NCT01388491PHASE2COMPLETEDA Multinational Study to Evaluate the Effects of a 28-Day Oral Contraceptive on Hemostatic Parameters in Healthy Women
NCT01500473PHASE2TERMINATEDTherapeutic Effect of Desogestrel on Ventilatory Control in Patients With Congenital Central Hypoventilation Syndrome
NCT01291004PHASE1COMPLETEDA Study to Evaluate Ovarian Follicular Activity and Hormone Levels for DR-102 Compared to Two 28-Day Oral Contraceptives
NCT03353857PHASE1COMPLETEDDrug-drug Interaction Between Rifampicin and Progestins/Ethinylestradiol and Midazolam
NCT04422028PHASE1COMPLETEDBioavailability of Desogestrel 0.075 mg Tablets With Regards to Reference Product
NCT07269327PHASE1COMPLETEDAn Ethno-bridging Study of Pergoveris in Healthy Premenopausal Participants of Japanese or Caucasian Origin
NCT00204438Not specifiedCOMPLETEDAdministration of Oral Contraceptives at Different Times of the Follicular Phase of the Menstrual Cycle
NCT01005056Not specifiedCOMPLETEDPost-marketing, Observational Study to Confirm the Safety and Efficacy of MARVELON (Study P06083)
NCT01559480Not specifiedCOMPLETEDPostoperative Desogestrel for Endometriosis Related Pain
NCT03398811Not specifiedCOMPLETEDAbnormal Uterine Bleeding and Progestin-only Contraceptives
NCT05174195Not specifiedTERMINATEDDoes Oral Desogestrel Prior to Insertion of the Etonogestrel Subdermal Implant Improve Continuation Rate at One Year?

Clinical evidence (CIViC)

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

Pharmacology

Pharmacogenomics

No CPIC/DPWG dosing guideline or drug-level clinical/variant annotations in PharmGKB for this molecule.

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