Promegestone

Promegestone, sold under the brand name Surgestone, is a progestin medication which is used in menopausal hormone therapy and in the treatment of gynecological disorders.[4][1][5][6] It is taken by mouth.[1]

Not to be confused with Progesterone (medication).
Promegestone
Clinical data
Trade namesSurgestone
Other namesPMG; R-5020; RU-5020; 17α,21-Dimethyl-δ9-19-norprogesterone; 17α,21-Dimethyl-19-norpregna-4,9-diene-3,20-dione
Routes of
administration		By mouth[1]
Drug classProgestogen; Progestin
ATC code
Pharmacokinetic data
Protein bindingTo albumin[1]
MetabolismLiver (hydroxylation)[1][2]
Metabolites• Trimegestone
Elimination half-lifePromegestone: ?
Trimegestone: 13.8–15.6 hours[1][3]
Identifiers
CAS Number
PubChem CID
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard100.207.681
Chemical and physical data
FormulaC22H30O2
Molar mass326.472 g/mol g·mol−1
3D model (JSmol)

Side effects of promegestone include menstrual irregularities among others.[7] Promegestone is a progestin, or a synthetic progestogen, and hence is an agonist of the progesterone receptor, the biological target of progestogens like progesterone.[1] It has weak antiandrogenic, glucocorticoid, and antimineralocorticoid activity and no other important hormonal activity.[1][8][3] The medication is largely a prodrug of trimegestone.[7][1]

Promegestone was first described in 1973 and was introduced for medical use in France in 1983.[9][10][11] It has only been marketed in a few countries, including France, Portugal, Tunisia, and Argentina.[6][12] In addition to its use as a medication, promegestone has been widely used in scientific research as a radioligand of the progesterone receptor.[4][13]

Medical uses

Promegestone is used in menopausal hormone therapy and in the treatment of gynecological conditions caused by luteal insufficiency, including premenopausal disorders, dysmenorrhea and other menstrual disorders, and premenstrual syndrome.[1][5][14] It has also been used to treat benign breast disorders such as mastalgia (breast pain).[15][14]

Side effects
See also: Progestin § Side effects

Side effects of promegestone include menstrual irregularities among others.[7] It has no androgenic side effects.[4][5]

Pharmacology

Pharmacodynamics
Trimegestone (21(S)-hydroxyl-promegestone), the major active metabolite of promegestone.

Promegestone is a progestogen, or an agonist of the progesterone receptor.[1][2] It has about 200% of the affinity of progesterone for the PR.[1][2] The endometrial transformation dosage of promegestone is 10 mg per cycle and its ovulation-inhibiting dosage is 0.5 mg/day.[1][2] Promegestone has weak glucocorticoid activity in addition to its progestogenic activity.[1][2] Conversely, it has no androgenic, estrogenic, mineralocorticoid, or other hormonal activity.[1][2][5] It appears to possess antiandrogenic activity.[13] Its major metabolite trimegestone has weak antimineralocorticoid and antiandrogenic activity.[8][3] In addition, promegestone has been found to possess some neurosteroid activity by acting as a non-competitive antagonist of the nicotinic acetylcholine receptor, similarly to progesterone.[16]

Pharmacokinetics

Following oral administration, peak serum levels of promegestone are reached after 1 to 2 hours.[1][2] The medication is mainly bound to albumin; it does not bind to sex hormone-binding globulin, and binds only weakly to corticosteroid-binding globulin.[1][2][17] The metabolism of promegestone is mainly via hydroxylation at the C21 position and at other positions.[1][2] Progesterone is similarly hydroxylated at the C21 position, into 11-deoxycorticosterone (21-hydroxyprogesterone).[18] However, the C9(10) double bond of promegestone greatly limits the A-ring reduction that progesterone undergoes, resulting in 21-hydroxylation being the main route of metabolism for promegestone.[18] The medication is stereoselectively metabolized into trimegestone, the 21(S)-hydroxy metabolite, which is the main compound found in plasma; it circulates at levels approximately twice those of promegestone itself.[7] In addition, trimegestone has more than three-fold higher affinity for the PR than does promegestone.[1] As such, promegestone is largely a prodrug of trimegestone.[7][19] A second metabolite, 21(R)-hydroxypromegestone, circulates at far lower concentrations (AUC ratio for the (S)- and (R)-isomers of about 21).[7] The elimination half-life of trimegestone is 13.8 to 15.6 hours.[1][3] Promegestone, trimegestone, and 21(R)-hydroxypromegestone are not excreted in urine, while 3% of a dose is recovered as the glucuronide and/or sulfate conjugate of trimegestone and 1% of a dose is recovered as the glucuronide and/or sulfate conjugate of 21(R)-hydroxypromegestone.[7]

Chemistry
See also: List of progestogens

Promegestone, also known as 17α,21-dimethyl-δ9-19-norprogesterone or as 17α,21-dimethyl-19-norpregna-4,9-diene-3,20-dione, is a synthetic norpregnane steroid and a derivative of progesterone.[9][12][11][1] It is specifically a combined derivative of 17α-methylprogesterone and 19-norprogesterone, or of 17α-methyl-19-norprogesterone.[9][11][1] Related derivatives of 17α-methyl-19-norprogesterone include demegestone and trimegestone.[9][12][1]

History

Promegestone was first described in the literature in 1973 and was introduced for medical use in France in 1983.[9][10][11][5] It was developed by Roussel Uclaf in France.[5]

Society and culture

Generic names

Promegestone is the generic name of the drug and its INN, while promégestone is its DCF.[6][9][12] It is also known by its developmental code name R-5020 or RU-5020.[6][9][12]

Brand names

Promegestone is marketed exclusively under the brand name Surgestone.[6][12][14]

Availability

Promegestone is or has been marketed in France, Portugal, Tunisia, and Argentina.[6][12][14]

References
  1. Kuhl, H (2005). "Pharmacology of estrogens and progestogens: influence of different routes of administration" (PDF). Climacteric. 8 (sup1): 3–63. doi:10.1080/13697130500148875. ISSN 1369-7137. PMID 16112947.
  2. Kuhl H (2011). "Pharmacology of progestogens" (PDF). Journal für Reproduktionsmedizin und Endokrinologie-Journal of Reproductive Medicine and Endocrinology. 8 (Special Issue 1): 157–176.
  3. Sitruk-Ware R, Bossemeyer R, Bouchard P (June 2007). "Preclinical and clinical properties of trimegestone: a potent and selective progestin". Gynecol. Endocrinol. 23 (6): 310–19. doi:10.1080/09513590701267727. PMID 17616854.
  4. Raynaud JP, Ojasoo T (1983). "[Promegestone, a new progestin]". J Gynecol Obstet Biol Reprod (Paris) (in French). 12 (7): 697–710. PMID 6366037.
  5. Cain (11 September 1984). ANNUAL REPORTS IN MED CHEMISTRY V19 PPR. Academic Press. pp. 323–. ISBN 978-0-08-058363-1.
  6. https://www.drugs.com/international/promegestone.html
  7. F.C. Tulunay; M. Orme (6 December 2012). European Collaboration: Towards Drug Developement [sic] and Rational Drug Therapy: Proceedings of the Sixth Congress of the European Association for Clinical Pharmacology and Therapeutics Istanbul, June 24–28, 2003. Springer Science & Business Media. pp. 107–. ISBN 978-3-642-55454-4. Investigation of the Pharmacokinetics and Metabolism of Promegestone in Healthy Female Volunteers Following Single Oral Administration of 1 mg Promegestone I Gualano V., 1Geneteau A., I Chassard D., I Fordham P., 2Schatz B. I Aster-Cephac, 3/5, Rue Eugene Millon, 75015 Paris, France 2Laboratoire Aventis, 46 Quai De La Rapee, F-75601 Paris Cedex 12, France. A single 1 mg oral dose of promegestone (Surgestonee, 2x0.5 mg) was given to 12 healthy premenopausal women. The aims were to determine the concentrations of promegestone and its metabolites and their pharmacokinet-ic parameters. Blood and urine samples were followed until 96 hours post dose. To avoid any interference with natural hormones, promegestone was given between day 7 and 10 of the menstrual cycle. Clinical safety and tolerability were good. Most of the minor adverse events observed were estimated possibly linked to the study drug (menstrual disorders) because classically related to progestins therapy. In addition, no clinically relevant biological modifications were observed. There was a stereoselective metabolism of promegestone in favor of the 21S hydroxy-promegestone, the main circulating compound in plasma (AUC ratio 5/R of about 21). Levels of 21S hydroxy-promegestone are about twice greater than that of unchanged promegestone. The plasma levels of the second metabolite, i.e. 21 R hydroxy-promegestone are far below these of either promegestone and 21S hydroxy-promegestone. Promegestone, 215 hydroxy- and 21R hydroxy-promegestone are not excreted in urine. About 3% of the dose was recov-ered in urine as sulfo and/or glucuro-conjugate 21S hydroxy-promegestone and about 1% of the dose as sulfo and/or glucuro conjugate 21R hydroxy-promegestone.
  8. Winneker RC, Bitran D, Zhang Z (2003). "The preclinical biology of a new potent and selective progestin: trimegestone". Steroids. 68 (10–13): 915–20. doi:10.1016/s0039-128x(03)00142-9. PMID 14667983.
  9. J. Elks (14 November 2014). The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer. pp. 1026–. ISBN 978-1-4757-2085-3.
  10. Philibert D, Raynaud JP (July 1973). "Progesterone binding in the immature mouse and rat uterus". Steroids. 22 (1): 89–98. doi:10.1016/0039-128x(73)90073-1. PMID 4353432.
  11. William Andrew Publishing (22 October 2013). Pharmaceutical Manufacturing Encyclopedia, 3rd Edition. Elsevier. pp. 2935–36. ISBN 978-0-8155-1856-3.
  12. Index Nominum 2000: International Drug Directory. Taylor & Francis. January 2000. pp. 883–. ISBN 978-3-88763-075-1.
  13. Raynaud, Jean-Pierre; Ojasoo, Tiiu; Vaché, Viviane (1981). "Stable and Specific Tracers": 163–179. doi:10.1007/978-1-4684-3824-6_7. Cite journal requires |journal= (help)
  14. http://www.micromedexsolutions.com/micromedex2/
  15. Uzan S, Denis C, Pomi V, Varin C (February 1992). "Double-blind trial of promegestone (R 5020) and lynestrenol in the treatment of benign breast disease". Eur. J. Obstet. Gynecol. Reprod. Biol. 43 (3): 219–27. doi:10.1016/0028-2243(92)90177-z. PMID 1563574.
  16. Blanton MP, Xie Y, Dangott LJ, Cohen JB (February 1999). "The steroid promegestone is a noncompetitive antagonist of the Torpedo nicotinic acetylcholine receptor that interacts with the lipid-protein interface". Mol. Pharmacol. 55 (2): 269–78. doi:10.1124/mol.55.2.269. PMID 9927618.
  17. Chan DW, Slaunwhite WR (May 1977). "The binding of a synthetic progestin, R5020 to transcortin and serum albumin". J. Clin. Endocrinol. Metab. 44 (5): 983–85. doi:10.1210/jcem-44-5-983. PMID 858781.
  18. Gerald Litwack (2 December 2012). Biochemical Actions of Hormones. Elsevier. pp. 314–. ISBN 978-0-323-15344-7.
  19. Howard J.A. Carp (9 April 2015). Progestogens in Obstetrics and Gynecology. Springer. pp. 34–. ISBN 978-3-319-14385-9.

Further reading
  • Raynaud JP, Ojasoo T (1983). "[Promegestone, a new progestin]". J Gynecol Obstet Biol Reprod (Paris) (in French). 12 (7): 697–710. PMID 6366037.
  • Brun G, Dargent D, Pontonnier G, Petrescou L (May 1984). "[Clinical use of promegestone, a progestational agent with high specificity for receptors]". Rev Fr Gynecol Obstet (in French). 79 (5): 423–26. PMID 6396815.
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