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ENCLOMIPHENE CITRATE VS. CLOMIPHENE CITRATE FOR MEN: RISKS VERSUS REWARDS

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ENCLOMIPHENE CITRATE VS. CLOMIPHENE CITRATE FOR MEN: RISKS VERSUS REWARDS

Introduction

Low testosterone (hypogonadism) and male infertility affect millions of men worldwide. As awareness of male reproductive health grows, patients and physicians alike are turning to alternatives to exogenous testosterone therapy—especially in men who desire to preserve fertility. Among the top contenders are two selective estrogen receptor modulators (SERMs): Clomiphene citrate and Enclomiphene citrate.

While Clomiphene has been used off-label for decades in men, Enclomiphene has recently garnered attention for its targeted mechanism and lower side-effect profile. But how do they compare? What are their differences in pharmacology, availability, impact on testosterone and fertility, and safety profiles? Are there medicolegal concerns physicians must consider when prescribing either, especially since both lack FDA approval for use in men?

This article explores these questions in-depth, helping patients and physicians make informed decisions.

What Are Clomiphene and Enclomiphene Citrate?

Clomiphene citrate (brand name: Clomid) is an FDA-approved medication for inducing ovulation in women, but it has been used off-label for male hypogonadism and infertility for over 40 years. Clomiphene is a racemic mixture of two isomers: Zuclomiphene (cis) and Enclomiphene (trans).

Enclomiphene citrate is the purified trans-isomer of clomiphene. It was investigated as a standalone treatment for secondary hypogonadism in men but has not received FDA approval despite completing Phase II and III trials under the brand name Androxal.

Both medications act as estrogen receptor antagonists in the hypothalamus, tricking the brain into thinking estrogen levels are low, thereby stimulating increased release of gonadotropins (LH and FSH) from the pituitary, which in turn increases endogenous testosterone and sperm production.

Pharmacology and Mechanism of Action

 

Clomiphene Citrate

  • Racemic mixture: 38% Enclomiphene (trans) and 62% Zuclomiphene (cis)

  • Half-lives:

    • Enclomiphene: ~10 hours

    • Zuclomiphene: ~30–50 days (can accumulate over time)

  • Action: Competitive inhibition of estrogen receptors in the hypothalamus increases GnRH → LH and FSH → testosterone and spermatogenesis

  • Drawback: The cis isomer (Zuclomiphene) has long-lasting estrogenic activity, possibly contributing to side effects like mood swings, gynecomastia, and decreased libido

Enclomiphene Citrate

  • Single isomer (trans) only

  • Shorter half-life (~10 hours) → Less accumulation

  • More potent stimulation of LH and FSH without residual estrogenic effects

  • Intended to mimic physiological diurnal testosterone rhythm more effectively than clomiphene

Key Difference: Enclomiphene provides more selective hypothalamic-pituitary stimulation, avoiding the long-acting estrogenic effects of Zuclomiphene.

Availability and FDA Status

Feature Clomiphene Citrate Enclomiphene Citrate
FDA-Approved Yes (for female infertility only) No (investigational in men; never approved)
Route Oral Oral (compounded)
Prescription in Men Off-label Compounded only (off-label use)
Commercial Name (Men) None Formerly Androxal (not marketed)

Clomiphene is widely available in generic form. Enclomiphene is not FDA-approved but is available through compounding pharmacies, usually under strict physician supervision.

Impact on Serum Testosterone and Sperm Production

Testosterone Levels

Both medications stimulate endogenous testosterone production.

  • Clomiphene increases testosterone by 100–200% in many men [1]

  • Enclomiphene has been shown to restore testosterone to mid-normal ranges (450–600 ng/dL) in hypogonadal men [2], with less suppression of LH and FSH than exogenous testosterone

A Phase III trial (Topline Study, 2015) demonstrated Enclomiphene significantly raised testosterone levels in men with secondary hypogonadism, comparable to injectable testosterone but with preserved fertility [3].

Spermatogenesis

Unlike exogenous testosterone (which often suppresses sperm production), both Clomiphene and Enclomiphene:

  • Stimulate FSH → Promotes Sertoli cell function and spermatogenesis

  • Maintain or improve sperm concentration, motility, and morphology

One study showed that 67% of azoospermic men treated with Clomiphene for 6 months developed sperm in ejaculate [4]. Enclomiphene has similar fertility-preserving effects, with early data suggesting slightly superior outcomes in sperm count maintenance [5].

Side Effects and Safety Profiles

Clomiphene Citrate

  • Mood changes, irritability, depression

  • Visual disturbances (blurred vision, floaters)

  • Gynecomastia

  • Fatigue, acne, weight gain

  • Rare: venous thromboembolism

These effects are believed to be due in part to accumulation of Zuclomiphene, the long-acting estrogenic isomer.

Enclomiphene Citrate

  • Fewer mood and visual side effects reported

  • No gynecomastia in trials

  • Less risk of estrogenic accumulation

  • Still requires regular liver function monitoring and hormonal profiling

Enclomiphene is generally better tolerated, with fewer CNS and estrogen-related effects, especially in long-term use.

Monitoring During Treatment

Monitoring Parameter Frequency Target
Total Testosterone Every 6–8 weeks 450–900 ng/dL
LH and FSH Baseline, then q3 months Should rise or remain steady
Estradiol Every 6–12 weeks < 40 pg/mL (balance required)
Semen Analysis q3–6 months Check sperm concentration, motility
Liver Function Tests Baseline, then annually ALT/AST within normal range
Prolactin Baseline if symptoms Should remain normal

Monitoring ensures efficacy, avoids overtreatment, and checks for adverse effects, particularly with long-term use.

Prescribing Patterns: How Common Are These Drugs in Men?

  • Clomiphene is widely prescribed off-label by urologists and reproductive endocrinologists for:

    • Secondary hypogonadism

    • Low testosterone with preserved fertility

    • Idiopathic male infertility

  • Enclomiphene is less commonly used, available only via compounding. Despite promising clinical trial results, it has not secured FDA approval, limiting its reach.

In a 2020 AUA survey of reproductive urologists, Clomiphene was the first-line medical therapy for men with secondary hypogonadism desiring fertility preservation [6].

Unique Characteristics: Pros and Cons

Clomiphene Citrate

Pros:

  • Generic and inexpensive

  • Well-studied in both men and women

  • Readily available

Cons:

  • Accumulation of Zuclomiphene

  • Estrogenic side effects (gynecomastia, mood swings)

  • Requires more careful monitoring of estradiol

Enclomiphene Citrate

Pros:

  • Targets only the active isomer

  • Rapid clearance = less accumulation

  • Lower incidence of estrogenic side effects

  • Preserves diurnal testosterone rhythm

Cons:

  • Not FDA approved

  • Must be compounded, increasing variability and cost

  • Limited long-term safety data

Legal and Liability Considerations

Off-Label Use

Both medications are used off-label in men, but with different risk implications:

  • Clomiphene citrate is FDA-approved for use in women, and its off-label use in men is widespread. It is supported by decades of research and is considered standard of care by many reproductive urologists.

  • Enclomiphene citrate, on the other hand, is not FDA-approved for any use and must be obtained via compounding pharmacies. Physicians who prescribe it take on a greater degree of legal liability, especially if adverse events occur.

Key Medicolegal Considerations

  • Informed consent is critical: Discuss with patients that neither drug is FDA-approved for men, and enclomiphene is compounded and not subjected to the same manufacturing standards.

  • Documentation: Clearly document rationale, discussions of risks/benefits, and informed consent.

Best practice: Consider developing a formal informed consent form specifically for off-label and compounded hormonal therapies.

Conclusion: Which One Should You Choose?

Both Clomiphene and Enclomiphene have a role in the management of male hypogonadism and infertility—particularly in men who wish to preserve fertility.

Criteria Clomiphene Enclomiphene
FDA Status Approved (women) Not approved
Use in Men Off-label Off-label compounded only
Sperm Preservation Yes Yes
Side Effects More estrogenic Fewer, shorter half-life
Monitoring Burden Moderate Moderate
Physician Liability Lower Higher (due to compounding)
Cost Lower Higher

Clomiphene citrate remains the first-line option due to availability, cost, and decades of clinical experience. However, enclomiphene citrate offers a promising alternative, particularly for men who experience side effects from Clomiphene or require a more physiologic testosterone profile.

Final Thoughts

For patients: If you are considering treatment for low testosterone and want to preserve fertility, both options can be effective. Discuss the pros and cons with your physician, including the regulatory status of each drug.

For physicians: Choose wisely, document thoroughly, and stay informed about evolving data. As personalized medicine evolves, so too will our options for treating male hypogonadism with fertility in mind.

References

  1. Katz, DJ et al. “Clomiphene Citrate and Testosterone Replacement Therapy for Male Hypogonadism: An Evidence-Based Review.” Current Urology Reports, 2012.

  2. Kaminetsky, J. et al. “The Efficacy of Enclomiphene Citrate in Men With Secondary Hypogonadism: Phase III Trials.” Journal of Clinical Endocrinology & Metabolism, 2015.

  3. Repros Therapeutics. “Androxal (Enclomiphene Citrate) Phase III Topline Data.” 2015.

  4. Hsieh, TC et al. “Clomiphene citrate effects on testosterone/estradiol ratio in male infertility.” Fertility and Sterility, 2005.

  5. Kim, ED et al. “Comparison of enclomiphene citrate versus transdermal testosterone in men with secondary hypogonadism.” Fertility and Sterility, 2015.

  6. AUA Male Reproductive Health Survey, 2020.