Enclomifene

Enclomifene (INNTooltip International Nonproprietary Name), or enclomiphene (USANTooltip United States Adopted Name), a nonsteroidal selective estrogen receptor modulator of the triphenylethylene group acts by antagonizing the estrogen receptor (ER) in the pituitary gland, which reduces negative feedback by estrogen on the hypothalamic-pituitary-gonadal axis, thereby increasing gonadotropin secretion and hence gonadal production of testosterone.[3] It is one of the two stereoisomers of clomifene, which itself is a mixture of 38% zuclomifene and 62% enclomifene.[3] Enclomifene is the (E)-stereoisomer of clomifene, while zuclomifene is the (Z)-stereoisomer.[4][5] Whereas zuclomifene is more estrogenic, enclomifene is more antiestrogenic.[3] In accordance, unlike enclomifene, zuclomifene is antigonadotropic due to activation of the ER and reduces testosterone levels in men.[3] As such, isomerically pure enclomifene is more favorable than clomifene as a progonadotropin for the treatment of male hypogonadism.[3]

Enclomifene
Clinical data
Trade namesAndroxal
Other namesEnclomiphene; (E)-Clomifene; RMI-16289; Enclomid; Enclomifene citrate; Enclomiphene citrate
Routes of
administration		By mouth
Drug classSelective estrogen receptor modulator; Progonadotropin
Pharmacokinetic data
Metabolismliver, CYP2D6 and CYP3A4[1]
Elimination half-life10 hours[2]
Identifiers
  • 2-[4-[(E)-2-chloro-1,2-diphenylethenyl]phenoxy]-N,N-diethylethanamine
CAS Number
PubChem CID
IUPHAR/BPS
DrugBank
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
Chemical and physical data
FormulaC26H28ClNO
Molar mass405.97 g·mol−1
3D model (JSmol)
  • CCN(CC)CCOC1=CC=C(C=C1)/C(=C(\C2=CC=CC=C2)/Cl)/C3=CC=CC=C3
  • InChI=1S/C26H28ClNO/c1-3-28(4-2)19-20-29-24-17-15-22(16-18-24)25(21-11-7-5-8-12-21)26(27)23-13-9-6-10-14-23/h5-18H,3-4,19-20H2,1-2H3/b26-25+
  • Key:GKIRPKYJQBWNGO-OCEACIFDSA-N

Enclomifene or Enclomiphene (former tentative brand names Androxal and EnCyzix), was under development for the treatment of male hypogonadism and type 2 diabetes.[4][5][6][3] By December 2016, it was in preregistration and was under review by the Food and Drug Administration in the United States and the European Medicines Agency in the European Union.[6] In January 2018, the Committee for Medicinal Products for Human Use of the European Medicines Agency recommended refusal of marketing authorization for enclomifene for the treatment of secondary hypogonadism.[7] In April 2021, development of enclomifene was discontinued for all indications.[6]

Clomiphene citrate, of which enclomiphene citrate is derived from, is a drug approved by the Food and Drug Association (FDA) for indications of anovulatory or oligo-ovulatory infertility and male infertility (spermatogenesis induction).[8]

A media release by the FDA for the pharmacy compounding advisory committee compared the efficacy of testosterone replacement therapy against enclomiphene. They wrote that while testosterone replacement therapy often resulted in side effects such as transference risk, supranormal testosterone levels, suppressed spermatogenesis, suppressed testicular function, and testicular atrophy, none of these risks are present in enclomiphene.[9]

In 2009, a study discovered that “short-term clinical safety data for enclomiphene have been satisfactory and equivalent to safety data for testosterone gels and placebo.”[10]

In 2016, a study on enclomiphene citrate reported that “the ability [of enclomiphene citrate] to treat testosterone deficiency in men while maintaining fertility supports a role for enclomiphene citrate in the treatment of men in whom testosterone therapy is not a suitable option.”[11]

In 2019, a study was published that found that “enclomiphene has been shown to increase testosterone levels while stimulating [follicular-stimulating hormone] and [luteinizing hormone] production.”[12]

The key difference between enclomiphene citrate and traditional testosterone replacement therapy is that enclomiphene citrate stimulates the body to produce its own testosterone, while traditional testosterone replacement therapy replaces low testosterone levels in men with exogenous, synthetic testosterone.

A study conducted in 2013 offered this assessment of the potential of enclomiphene citrate to increase sexual function in men: “If enclomiphene citrate can correct the central defect in men that blocks their ability to produce [lutenizing hormone] and [follicular-stimulating hormone] and thus to produce both testosterone and sperm in the testes, this drug may prove itself superior to other treatments.”[13]

Mechanism of action

Enclomiphene is a selective estrogen receptor antagonist, antagonizing the estrogen receptors in the pituitary gland, disrupting the negative feedback loop by estrogen towards the hypothalamic-pituitary-gonadal axis, ultimately resulting in an increase in gonadotropin secretion.

In men with secondary hypogonadotropic hypogonadism, this improves testosterone levels and sperm motility. Men with secondary hypogonadotropic hypogonadism have abnormally low testosterone levels due to low-normal levels of luteinizing hormone (LH) and follicular stimulating hormone (FSH). The biological role of these hormones is to stimulate the endogenous production of testosterone by the testes.

Common symptoms of secondary hypogonadotropic hypogonadism include low libido, energy, and mood. In addition, men with low testosterone may experience osteoporosis, an increase in visceral fat, and the regression of secondary sexual characteristics.[13] Enclomiphene stimulates the endogenous production of testosterone. It works differently from traditional testosterone replacement therapy, which replaces testosterone using an exogenous source.

In addition, research has uncovered that enclomiphene increases total and free testosterone levels without increasing dihydrotestosterone disproportionately, suggesting that it “normalizes endogenous testosterone production pathways and restores normal testosterone levels in men with secondary hypogonadism.”[14]

Medical uses

Enclomiphene is primarily used as a treatment for men with persistent low testosterone as a result of secondary hypogonadotropic hypogonadism. In secondary hypogonadotropic hypogonadism, the resulting low levels of testosterone is attributed to inadequacies in the hypothalamic-pituitary-gonadal axis. In contrast, primary hypogonadism is caused by defects in the testes that causes them to be unable to produce the required amount of testosterone.

Enclomiphene, which stimulates the endogenous production of testosterone, is not currently known to have common adverse effects of exogenous testosterone replacement therapy, such as reduced spermatogenesis or infertility.[15][16]

Contraindications

Enclomiphene citrate is contraindicated in patients with a known hypersensitivity or allergy to enclomiphene citrate or any of its ingredients. An uncontrolled allergic reaction to a medication can result in serious health complications and even death.

In addition, enclomiphene citrate is contraindicated in the groups of individuals below:

  • Pregnant women.
  • Breastfeeding women.
  • Women with unexplained uterine bleeding.
  • Women with ovarian growths or cysts unrelated to polycystic ovary syndrome.
  • Patients with a history of liver disease.
  • Patients with uncontrolled adrenal or thyroid dysfunction.
  • Patient with known allergy to enclomiphene or clomiphene.

Adverse effects

Studies conducted on the adverse effects of enclomiphene have discovered that the drug is generally well-tolerated. There were concerns about a possible increase in risk for venous thromboembolism, but the incidence has been discovered to be very low.[12]

Adverse Event Percentage (%)
Headache

Nausea

Arthralgia

Diarrhea

Nasopharyngitis

Hot flushes

Dizziness

3.3

2.1

1.2

1.9

1.7

1.7

1

The report also discovered that the rate of serious adverse effects was lower in the enclomiphene group compared to the placebo group when adjusted for subject exposure years.[12] There has been no reports that enclomiphene causes infertility or decreased spermatogenesis.

References
  1. Ghobadi C, Gregory A, Crewe HK, Rostami-Hodjegan A, Lennard MS (2008). "CYP2D6 is primarily responsible for the metabolism of clomiphene". Drug Metabolism and Pharmacokinetics. 23 (2): 101–105. doi:10.2133/dmpk.23.101. PMID 18445989.
  2. Mikkelson TJ, Kroboth PD, Cameron WJ, Dittert LW, Chungi V, Manberg PJ (September 1986). "Single-dose pharmacokinetics of clomiphene citrate in normal volunteers". Fertility and Sterility. 46 (3): 392–396. doi:10.1016/s0015-0282(16)49574-9. PMID 3091405.
  3. Hill S, Arutchelvam V, Quinton R (February 2009). "Enclomiphene, an estrogen receptor antagonist for the treatment of testosterone deficiency in men". IDrugs. 12 (2): 109–119. PMID 19204885.
  4. J. Elks (14 November 2014). The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer. pp. 298–. ISBN 978-1-4757-2085-3.
  5. I.K. Morton; Judith M. Hall (31 October 1999). Concise Dictionary of Pharmacological Agents: Properties and Synonyms. Springer Science & Business Media. pp. 79–. ISBN 978-0-7514-0499-9.
  6. "Enclomifene - Repros Therapeutics - AdisInsight".
  7. "EnCyzix". 17 September 2018.
  8. Mbi Feh MK, Wadhwa R (2022). "Clomiphene". StatPearls. Treasure Island (FL): StatPearls Publishing. PMID 32644718. Retrieved 2022-11-29.
  9. Elsaied M. "Enclomiphene Citrate". Food and Drug Administration.
  10. Hill S, Arutchelvam V, Quinton R (February 2009). "Enclomiphene, an estrogen receptor antagonist for the treatment of testosterone deficiency in men". IDrugs. 12 (2): 109–119. PMID 19204885.
  11. Rodriguez KM, Pastuszak AW, Lipshultz LI (August 2016). "Enclomiphene citrate for the treatment of secondary male hypogonadism". Expert Opinion on Pharmacotherapy. 17 (11): 1561–1567. doi:10.1080/14656566.2016.1204294. PMC 5009465. PMID 27337642.
  12. Earl JA, Kim ED (May 2019). "Enclomiphene citrate: A treatment that maintains fertility in men with secondary hypogonadism". Expert Review of Endocrinology & Metabolism. 14 (3): 157–165. doi:10.1080/17446651.2019.1612239. PMID 31063005. S2CID 146811440.
  13. Kaminetsky J, Werner M, Fontenot G, Wiehle RD (June 2013). "Oral enclomiphene citrate stimulates the endogenous production of testosterone and sperm counts in men with low testosterone: comparison with testosterone gel". The Journal of Sexual Medicine. 10 (6): 1628–1635. doi:10.1111/jsm.12116. PMID 23530575.
  14. Wiehle RD, Fontenot GK, Willett MS, Garcia WD, Podolski JS (2014-12-01). "Enclomiphene Citrate Stimulates Serum Testosterone in Men With Low Testosterone Within 14 Days". Journal of Men's Health. 11 (4): 196–205. doi:10.1089/jomh.2014.0006. ISSN 1875-6867.
  15. Khodamoradi K, Khosravizadeh Z, Parmar M, Kuchakulla M, Ramasamy R, Arora H (January 2021). "Exogenous testosterone replacement therapy versus raising endogenous testosterone levels: current and future prospects". F&S Reviews. 2 (1): 32–42. doi:10.1016/j.xfnr.2020.11.001. PMC 7894643. PMID 33615283.
  16. Yazdani N, Matthews Branch S (March 2018). "Daily subcutaneous testosterone for management of testosterone deficiency". Frontiers in Bioscience. 10 (2): 334–343. doi:10.2741/e825. PMID 29293461.
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