library.onepin.app/enclomiphene Peptide Education Library
Education only, not medical advice 21+ Every dose is an example to finalize with a licensed provider

OnePin Peptide Library · Hormonal

Hormonal SERM Not FDA-approved · investigational Controlled substance

Enclomiphene

Encolomid · Androxal

SERMHormonal

Enclomiphene is the trans-isomer of clomiphene citrate, a selective estrogen receptor modulator (SERM). While clomiphene citrate (Clomid) is a racemic mixture of enclomiphene (trans) and zuclomiphene (cis), enclomiphene is the isomer primarily responsible for the anti-estrogenic effects at the hypothalamic-pituitary level that stimulate gonadotropin release and subsequently testosterone production in men.,Enclomiphene was developed by Repros Therapeutics (later Rennova Health) under the brand name Androxal specifically for the treatment of secondary hypogonadism in men - a condition where testosterone is low due to insufficient gonadotropin signaling rather than primary testicular failure. Unlike testosterone replacement therapy (TRT), enclomiphene stimulates the body's own testosterone production while preserving spermatogenesis and fertility, making it particularly attractive for younger men who wish to maintain reproductive capacity.,Despite promising Phase 3 clinical trial results showing significant testosterone elevation while maintaining sperm parameters, the FDA issued a Complete Response Letter (CRL) in 2015 citing manufacturing and formulation concerns rather than efficacy or safety issues. Enclomiphene has not received FDA approval as of 2025, though it is widely used off-label through compounding pharmacies and men's health clinics. Generic clomiphene citrate is sometimes used as an alternative, though it contains the zuclomiphene isomer which has a much longer half-life and estrogenic properties.

Quick Start
Route
Oral
Start low
12.5-25mg
Frequency
daily
Timing
Can be taken with or without food

Start here. Every protocol below is ordered lowest-first. Begin at the smallest effective dose, hold about a week to assess tolerance, and step up only if needed.

Tiered Protocols · lowest first
Quick Start
Conservative start
12.5-25mg · Oral · daily
Lowest starting point. Hold about a week to assess tolerance before stepping up.
12.5-25mg
daily
Standard
HPTA Stimulation / TRT Alternative
6.25-12.5 mg · Oral · Daily
human clinical trial · Kaminetsky et al. 2013 (J Sex Med)
6.25-12.5 mg
Daily
Reconstitution CalculatorU-100
050100u
Draw to
units
01

How it works

Competitively blocks estrogen receptors in the hypothalamus and anterior pituitary, preventing the negative feedback of estradiol on GnRH and gonadotropin secretion. This disinhibition leads to increased pulsatile GnRH release and subsequent elevations in LH and FSH.,Elevated LH stimulates Leydig cells in the testes to produce more testosterone, while elevated FSH supports Sertoli cell function and spermatogenesis, preserving both hormonal and reproductive function.,Unlike zuclomiphene (the cis-isomer), enclomiphene has a short half-life (~10 hours) and primarily anti-estrogenic activity, avoiding the prolonged estrogenic effects and accumulation associated with racemic clomiphene.

Competitively blocks estrogen receptors in the hypothalamus and anterior pituitary, preventing the negative feedback of estradiol on GnRH and gonadotropin secretion. This disinhibition leads to increased pulsatile GnRH release and subsequent elevations in LH and FSH.,Elevated LH stimulates Leydig cells in the testes to produce more testosterone, while elevated FSH supports Sertoli cell function and spermatogenesis, preserving both hormonal and reproductive function.,Unlike zuclomiphene (the cis-isomer), enclomiphene has a short half-life (~10 hours) and primarily anti-estrogenic activity, avoiding the prolonged estrogenic effects and accumulation associated with racemic clomiphene.

02

What to expect

Early
Days 1–7

Weeks 1-2: Gonadotropins (LH, FSH) begin rising within days. Testosterone elevation begins but subjective effects are typically minimal.

03

Evidence

HumanPresent
AnimalPresent
In-vitroPresent
2014Enclomiphene citrate stimulates testosterone production while preventing oligospermia: a randomized phase II clinical trial comparing topical testosterone · Wiehle RD, Fontenot GK, Wike J, et al, Fertility and Sterility ↗peer reviewed
2013Testosterone restoration using enclomiphene citrate in men with secondary hypogonadism: a pharmacodynamic and pharmacokinetic study · Kaminetsky J, Werner M, Fontenot G, Wiehle RD, BJU International ↗peer reviewed
2016Oral enclomiphene citrate raises testosterone and preserves sperm counts in obese hypogonadal men, unlike topical testosterone · Kim ED, McCullough A, Kaminetsky J, BJU International ↗peer reviewed
2016Enclomiphene citrate for the treatment of secondary male hypogonadism · Earl JA, Kim ED, Expert Review of Clinical Pharmacology ↗review
04

Interactions & stacking

What's safe to combine, and what belongs in a separate pin.

Safe & synergistic

EpicatechinNo interaction - enclomiphene supports testosterone while epicatechin targets myostatin/follistatin independently
L-Carnitine InjectableNo pharmacological conflict - carnitine supports fat metabolism independent of SERM activity
MelatoninNo interaction - different systems (circadian vs reproductive axis)
Injectable B-ComplexB vitamins support energy metabolism - no interaction with SERM mechanism

Keep separate

Testosterone CypionateExogenous testosterone suppresses LH/FSH via negative feedback - directly counteracts enclomiphene's mechanism of stimulating endogenous production
HCGHCG provides exogenous LH-like stimulation - combining with enclomiphene creates redundant gonadotropin stimulation with unpredictable E2 elevation
Nandrolone DecanoateExogenous anabolic steroids suppress the HPG axis - negates enclomiphene's mechanism of restoring endogenous testosterone
TriptorelinGnRH agonist at continuous doses suppresses LH/FSH - directly opposes enclomiphene's mechanism
05

Pharmacokinetics

Illustrative plasma concentration · 24 h
Half-life
~10 hours
Peak · Tmax
~2-4 hours oral
Elimination
~2-3 days
Activity
24 hours (estrogen receptor blockade supports daily dosing; LH/FSH elevation persists throughout the day)

Storage. Store at room temperature (20-25C) in a cool, dry place. Oral compound - no reconstitution needed.

06

Regulatory status

Not FDA-approved. Received Complete Response Letter in 2015 for manufacturing issues. Widely available through US compounding pharmacies. Used off-label by men's health and hormone optimization clinics. Not a controlled substance in the US.

Put it to work

Calculate, log & track

Open Enclomiphene straight into OnePin with your vial and dose pre-filled, then let it handle the syringe math and remind you before the vial runs out.

Open Enclomiphene in the app →

Go deeper

The guide & community

The complete Enclomiphene walkthrough, real protocol discussion and coaching live inside the BlessUp community on Skool.

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