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Enclomiphene

Experience the power of transformation with Enclomiphene – your path to renewed vigor and peak performance awaits.

In Men, Enclomiphene's primary role is to block estrogen receptors in the hypothalamus, leading to an increase in the secretion of gonadotropin-releasing hormone (GnRH). This, in turn, stimulates the release of luteinizing hormone (LH) from the pituitary gland, prompting the testes to produce more testosterone.

Enclomiphene, a selective estrogen receptor modulator (SERM), operates by binding to estrogen receptors in the hypothalamus, a region of the brain that plays a crucial role in regulating hormonal balance. By doing so, enclomiphene blocks the negative feedback effects of estrogen, leading to an increase in the secretion of gonadotropin-releasing hormone (GnRH). This heightened GnRH production subsequently stimulates the release of follicle-stimulating hormone (FSH) and luteinizing hormone (LH), ultimately leading to the stimulation of testosterone production in men.

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The science of Enclomiphene

Active ingredients

Enclomiphene citrate, the active pharmaceutical ingredient, is the primary component of enclomiphene. It's formulated with inactive ingredients like microcrystalline cellulose, lactose monohydrate, magnesium stearate, and colloidal silicon dioxide to form tablets for oral administration.

Mechanism

Enclomiphene is administered orally in tablet form. The recommended dosage and duration of treatment vary based on the specific medical condition being addressed and goals of treatment. A Superpower physician will prescribe in individual protocol including dosing plans, follow-up testing, and surveys to ensure proper monitoring and adjustment of the treatment plan if necessary.

History

Enclomiphene, is a non-FDA-approved medication that has garnered attention for its off-label application in the treatment of hypogonadism in males. It is an isomer of Clomiphene Citrate (brand name: Clomid), an FDA approved medication for the indication ovulatory dysfunction in women desiring pregnancy.  Unlike its conventional use, enclomiphene's potential in managing low testosterone levels is a newer exploration. While the FDA has not specifically approved enclomiphene for hypogonadism, healthcare professionals consider its use for this purpose.A growing body of evidence suggests that enclomiphene may be a rapid and more effective treatment than Clomiphene citrate for treating secondary hypogonadism in men.  Male secondary hypogonadism is a clinical syndrome caused by androgen deficiency attributed to the hypothalamic-pituitary-gonadal (HPG) axis. Initial studies indicate that Enclomiphene citrate possesses distinct advantages over Clomid (clomiphene citrate) and aromatase inhibitors for managing secondary hypogonadism. Firstly, enclomiphene citrate is the trans-isomer of clomiphene citrate and exhibits higher potency in stimulating the hypothalamic-pituitary-gonadal axis. This improved specificity enables enclomiphene citrate to effectively increase testosterone levels while minimizing estrogen-related side effects. Moreover, unlike aromatase inhibitors, enclomiphene citrate does not inhibit the aromatase enzyme responsible for converting testosterone into estrogen. This property allows enclomiphene citrate to maintain appropriate estrogen levels, contributing to better overall hormonal balance.

How to get Enclomiphene

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