Enclomiphene
Enclomiphene is the trans-isomer of clomiphene citrate (clomid), isolated from the racemic mixture to provide the active estrogen-antagonist component without the estrogenic zuclomiphene (cis-) isomer. It is a selective estrogen receptor modulator (SERM) that blocks estrogen negative feedback at the hypothalamus and pituitary, resulting in increased LH and FSH secretion — which stimulates the testes to produce testosterone. Unlike exogenous testosterone, it maintains the entire HPG axis and preserves fertility (sperm production continues). Phase III trials in secondary hypogonadism showed testosterone normalization while preserving semen parameters. Often favored over TRT by younger men and those planning families.
Evidence
No score yet
Safety
Unknown safety profile
Clinical Status
No formal phase listed
Last Sync
Not synced yet
Last Reviewed
Not reviewed yet
Physician Notes
Preferred over clomiphene (Clomid) because the trans-isomer avoids the estrogenic side effects of the cis-isomer (zuclomiphene). Good option for younger men who want testosterone optimization without exogenous testosterone.
Monitoring
- Total T + Free T q3mo
- LH/FSH q3mo
- Estradiol q3mo
- Semen analysis if fertility-focused
Contraindications
- Liver disease
- Known hypersensitivity to clomiphene compounds
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Pharmacology
Evidence Score
Plain-English Snapshot
Enclomiphene is currently categorized as a hormonal compound.
Evidence scoring has not been fully computed yet, so interpret this profile as preliminary.
Safety scoring is incomplete. Start conservatively and monitor carefully.
Core mechanism
Blocks ER-alpha in hypothalamus and pituitary, reducing estrogen negative feedback; pulsatile GnRH/LH/FSH increase drives testicular testosterone production and spermatogenesis
Practical Context
Strongest current signals
No indexed study summaries yet.