Kyzatrex by is a Prescription medication manufactured, distributed, or labeled by Marius Pharmaceuticals, Procaps S A. Drug facts, warnings, and ingredients follow.
Capsules: 100 mg, 150 mg, 200 mg ( 3).
Most common adverse reactions (incidence ≥ 2%): hypertension ( 6.1).
To report SUSPECTED ADVERSE REACTIONS, contact Marius Pharmaceuticals at 1-833-949-5040 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.
Geriatric Patients: Geriatric patients treated with androgens may also be at risk for worsening of signs and symptoms of BPH and hypertension ( 8.5).
See 17 for PATIENT COUNSELING INFORMATION and Medication Guide.
KYZATREX™ is indicated for testosterone replacement therapy in adult males for conditions associated with a deficiency or absence of endogenous testosterone:
Limitations of Use
Safety and efficacy of KYZATREX™ in males less than 18 years old have not been established [see Use in Specific Populations (8.4)] .
KYZATREX™ is not substitutable with other oral testosterone undecanoate products.
Prior to initiating KYZATREX™, confirm the diagnosis of hypogonadism by ensuring that serum testosterone concentrations have been measured in the morning on at least two separate days and that these testosterone concentrations are below the normal range.
Individualize the dosage of KYZATREX™ based on the patient's serum testosterone concentration response to the drug.
The recommended starting dose is 200 mg orally twice daily, once in the morning and once in the evening. Take KYZATREX™ with food.
Check serum testosterone concentrations 7 days after starting treatment or after dosage adjustment, 3 to 5 hours after the morning dose. Adjust the KYZATREX™ dose as necessary as shown in Table 1. Thereafter, periodically monitor serum testosterone concentrations.
The minimum recommended dose is 100 mg once daily in the morning. The maximum recommended dose is 400 mg twice daily. For total daily doses greater than 100 mg, administer the same dose in the morning and evening.
|Serum Testosterone Concentration||Current KYZATREX™ Dosage||New KYZATREX™ Dosage|
|Less than 460 ng/dL||100 mg with breakfast only||100 mg twice daily with meals|
|100 mg twice daily with meals||200 mg twice daily with meals|
|200 mg twice daily with meals||300 mg twice daily with meals|
|300 mg twice daily with meals||400 mg twice daily with meals|
|460 to 971 ng/dL||No Dosage Change|
|More than 971 ng/dL||400 mg twice daily with meals||300 mg twice daily with meals|
|300 mg twice daily with meals||200 mg twice daily with meals|
|200 mg twice daily with meals||100 mg twice daily with meals|
|100 mg twice daily with meals||100 mg with breakfast only|
|100 mg with breakfast only||Discontinue treatment|
KYZATREX™ is contraindicated in:
In Study MRS-TU-2019EXT, KYZATREX™ increased 24-hour average systolic blood pressure (SBP) measured by ambulatory blood pressure monitoring (ABPM) by 1.7 mmHg from baseline after 4 months of treatment and 1.8 mmHg from baseline after 6 months of treatment [see Adverse Reactions (6.1)] . Three percent of KYZATREX™-treated patients were started on antihypertensive medications during the 6-month trial.
A history of antihypertensive treatment and diabetes mellitus at baseline were significant factors related to ambulatory SBP increases [see Adverse Reactions (6.1)] .
Blood pressure (BP) increases can increase the risk of major adverse cardiovascular events (MACE), with greater risk in patients with established cardiovascular disease or risk factors for cardiovascular disease. In some patients, the increase in BP with KYZATREX™ may be too small to detect but can still increase the risk for MACE.
Before initiating KYZATREX™, consider the patient's baseline cardiovascular risk and ensure blood pressure is adequately controlled. Check BP periodically after initiating KYZATREX™ or increasing the dose and thereafter. Treat new-onset hypertension or exacerbations of pre-existing hypertension. Re-evaluate whether the benefits of continued treatment with KYZATREX™ outweigh its risks in patients who develop cardiovascular risk factors or cardiovascular disease.
Androgens, including KYZATREX™, can cause increase in hemoglobin or hematocrit, reflective of increase in red blood cell mass. Check hematocrit prior to initiating KYZATREX™. An increase in red blood cell mass may increase the risk of thromboembolic events [see Warnings and Precautions (5.5)] . Evaluate hematocrit approximately every 3 months while the patient is on KYZATREX™. If hematocrit becomes elevated, stop KYZATREX™ until the hematocrit decreases to an acceptable concentration. If KYZATREX™ is restarted and again causes hematocrit to become elevated, permanently discontinue KYZATREX™.
Long-term clinical safety trials have not been conducted to assess the cardiovascular outcomes of testosterone replacement therapy in men. To date, epidemiologic studies and randomized controlled trials have been inconclusive for determining the risk of MACE, such as non-fatal myocardial infarction, non-fatal stroke, and cardiovascular death, with testosterone use compared to non-use. Some studies have reported an increased risk of MACE in association with use of testosterone replacement therapy in men.
KYZATREX™ can cause BP increases that can increase the risk of MACE [see Warnings and Precautions (5.1)] . Patients should be informed of this possible risk when deciding whether to use or to continue to use KYZATREX™.
There have been post-marketing reports of venous thromboembolic events, including deep vein thrombosis (DVT) and pulmonary embolism (PE), in patients using testosterone replacement products such as KYZATREX™. Evaluate patients who report symptoms of pain, edema, warmth, and erythema in the lower extremity for DVT and those who present with acute shortness of breath for PE. If a venous thromboembolic event is suspected, discontinue KYZATREX™ and initiate appropriate workup and management [see Adverse Reactions (6.2)].
Testosterone has been subject to abuse, typically at doses higher than recommended for the approved indication and in combination with other anabolic androgenic steroids. Anabolic androgenic steroid abuse can lead to serious cardiovascular and psychiatric adverse reactions [see Drug Abuse and Dependence (9)].
If testosterone abuse is suspected, check testosterone concentrations to ensure they are within therapeutic range [see Dosage and Administration (2.2)]. Testosterone levels may remain in the normal or subnormal range in men abusing synthetic testosterone derivatives. Counsel patients concerning the serious adverse reactions associated with abuse of testosterone and anabolic androgenic steroids. Also consider the possibility of testosterone and anabolic androgenic steroid abuse in suspected patients who present with serious cardiovascular or psychiatric adverse events.
With large doses of exogenous androgens, including KYZATREX™, spermatogenesis may be suppressed through feedback inhibition of pituitary FSH, possibly leading to adverse effects on semen parameters including sperm count [see Use in Specific Populations (8.3)]. Inform patients of this possible risk when deciding whether to use or to continue to use KYZATREX™.
KYZATREX™ is not a 17-alpha-alkyl androgen and is not known to cause hepatic adverse effects. However, prolonged use of high doses of orally active 17-alpha-alkyl androgens (e.g., methyltestosterone) has been associated with serious hepatic adverse effects (peliosis hepatis, hepatic neoplasms, cholestatic hepatitis, and jaundice). Peliosis hepatis can be a life-threatening or fatal complication. Long-term therapy with intramuscular testosterone enanthate has produced multiple hepatic adenomas. Patients should be instructed to report any signs or symptoms of hepatic dysfunction (e.g., jaundice). If these occur, promptly discontinue KYZATREX™ while the cause is evaluated.
Androgens, including KYZATREX™, may promote retention of sodium and water. Edema, with or without congestive heart failure, may be a serious complication in patients with pre-existing cardiac, renal, or hepatic disease [see Adverse Reactions (6.1)] . In addition to discontinuation of the drug, diuretic therapy may be required.
The treatment of hypogonadal men with testosterone may potentiate sleep apnea in some patients, especially those with risk factors such as obesity or chronic lung disease.
In clinical trials, patients receiving KYZATREX™ experienced reductions in lipid parameters, including total cholesterol, LDL cholesterol, HDL cholesterol, and triglycerides [see Adverse Reactions (6.1)] . Changes in the serum lipid profile may require dose adjustment of lipid lowering drugs or discontinuation of testosterone therapy. Monitor the lipid profile periodically, particularly after starting testosterone therapy.
Androgens, including KYZATREX™, should be used with caution in cancer patients at risk of hypercalcemia (and associated hypercalciuria). Monitor serum calcium concentrations periodically during treatment with KYZATREX™ in these patients.
Androgens, including KYZATREX™, may decrease concentrations of thyroxin-binding globulin, resulting in decreased total T4 serum concentrations and increased resin uptake of T3 and T4. Free thyroid hormone concentrations remain unchanged, however, and there is no clinical evidence of thyroid dysfunction.
The following clinically significant adverse reactions are discussed elsewhere in the labeling:
Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice.
The safety of KYZATREX™ was evaluated in Study MRS-TU-2019EXT in 155 hypogonadal males [see Clinical Studies (14)]. All patients initially received KYZATREX™ 200 mg orally twice daily. If needed, the dosage was titrated to 100 mg once daily in the morning or 100 mg, 300 mg, or 400 mg twice daily to achieve testosterone concentrations in the normal range . After the dosage titration period, patients continued their optimized dose for the remainder of the duration of the 6-month study. The mean duration of exposure was 168 days (range: 1 to 180 days). The median age was 52 years (range: 22 to 66 years); 77% were White, 19% were Black, 3% were Asian, and 2% were American Indian, Alaskan Native or Other.
Table 2 summarizes adverse reactions reported in ≥2% of patients in this 6-month study.
|Adverse Reaction||N = 155
|Hypertensión *||4 (2.6)|
One (0.8%) patient who received KYZATREX™ experienced an adverse reaction (acne) that lead to premature discontinuation from the study.
In a 12-month, open-label study in hypogonadal adult males (N=212) who received KYZATREX™ 200 mg once daily to 400 mg twice daily (n=202) the following additional adverse reactions were reported: headache, arthralgia, diarrhea, hemoglobin increased, anxiety, constipation, peripheral edema, and PSA increased.
Blood Pressure Increases
Ambulatory (24-hour) and in-clinic (cuff) blood pressure Changes from Baseline for study MRS-TU-2019EXT are presented in Table 3 with 95% confidence intervals. No significant difference was observed between the 4-month and 6-month Changes from Baseline.
|Blood Pressure||Change from Baseline (95% CI) mm Hg|
|4 Month||1.7 (0.3 to 3.1)||0.6 (-0.3 to 1.6)|
|6 Month||1.8 (0.3 to 3.2)||0.6 (-0.4 to 1.6)|
|In-clinic (blood pressure cuff)|
|4 Month||2.7 (0.9 to 4.5)||1.5 (0.3 to 2.6)|
|6 Month||2.4 (0.6 to 4.2)||1.7 (0.5 to 2.9)|
A total of 5 of 155 patients (3.2%) in Study MRS-TU-2019EXT began taking new antihypertensive medications after study start. No patient had a dose increase in their antihypertensive medication by the end of treatment.
A history of antihypertensive treatment and diabetes mellitus at baseline were significant factors related to ambulatory SBP increases.
Table 4 presents the Least Squares Mean estimates of Change from Baseline, with 95% CI's, for sub-populations of subjects at study start either with or without hypertensive treatment or with or without diabetes mellitus.
|Subgroups||Ambulatory Systolic Blood Pressure Change from Baseline (95% CI), mm Hg|
|With hypertensive treatment at baseline (n=49)|
|4 Month||3.4 (1.0 to 5.9)|
|6 Month||3.1 (0.6 to 5.6)|
|Without hypertensive treatment at baseline (n=90)|
|4 Month||0.7 (-1.0 to 2.4)|
|6 Month||1.0 (-0.7 to 2.8)|
|With diabetes at baseline (n=29)|
|4 Month||3.0 (-0.2 to 6.2)|
|6 Month||3.4 (0.2 to 6.7)|
|Without diabetes at baseline (n=110)|
|4 Month||1.3 (-0.2 to 2.9)|
|6 Month||1.3 (-0.3 to 2.9)|
Heart Rate Increases
KYZATREX™ increased mean (95%CI) 24-hour ambulatory heart rate by an average of 0.7 (-0.5 to 1.9) beats per minute (bpm) at 4 months and 1.9 (0.6 to 3.1) bpm at 6 months in Study MRS-TU-2019EXT. Changes in heart rate were similar between patients with or without hypertension or diabetes. Changes in heart rate with treatment were most prominent in the evening, 12 to 17 hours after the morning dose.
Increases in Hemoglobin
Increases in hemoglobin were reported in 7 out of 155 patients (4.5%) in Study MRS-TU2019EXT. None of these increases led to premature discontinuation of KYZATREX™.
Hematocrit was not assessed in this study.
Headaches were reported in 3 of 155 patients (1.9%) receiving KYZATREX™ in Study MRSTU-2019EXT.
Increases in Serum PSA
Four out of 155 patients (2.6%) receiving KYZATREX™ in Study MRS-TU-2019EXT had an increase in PSA from baseline greater than 1.4 ng/mL and two out of 155 patients (1.3%) had a PSA of at least 4.0 ng/mL during Study MRS-TU-2019EXT. The mean (SE) increase in PSA from baseline was 0.15 (±0.04) ng/mL at 6 months (n=135).
The following adverse reactions have been identified during post-approval use of testosterone. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure.
Cardiovascular Disorders: myocardial infarction, stroke
Vascular Disorders: Venous thromboembolism
Changes in insulin sensitivity or glycemic control may occur in patients treated with androgens. In diabetic patients, the metabolic effects of androgens may decrease blood glucose and therefore necessitate a decrease in the dose of anti-diabetic medication.
Changes in anticoagulant activity may be seen with androgens; therefore, more frequent monitoring of international normalized ratio (INR) and prothrombin time are recommended in patients taking warfarin, especially at the initiation and termination of androgen therapy.
The concurrent use of testosterone with corticosteroids may result in increased fluid retention and requires careful monitoring particularly in patients with cardiac, renal, or hepatic disease.
Some prescription medications and nonprescription analgesic and cold medications contain drugs known to increase blood pressure. Concomitant administration of these medications with KYZATREX™ may lead to additional increases in blood pressure [see Warnings and Precautions (5.1)].
KYZATREX™ is contraindicated in pregnant women and not indicated for use in females [see Contraindications (4)]. Testosterone is teratogenic and may cause fetal harm when administered to a pregnant woman based on data from animal studies (see Data) and its mechanism of action [see Clinical Pharmacology (12.1)]. Exposure of a female fetus to androgens may result in varying degrees of virilization. In animal developmental studies, exposure to testosterone in utero resulted in hormonal and behavioral changes in offspring and structural impairments of reproductive tissues in female and male offspring. These studies do not meet current standards for nonclinical development toxicity studies.
In developmental studies conducted in rats, rabbits, pigs, sheep, and rhesus monkeys, pregnant animals received intramuscular injections of testosterone during the period of organogenesis. Testosterone treatment at doses that were comparable to those used for testosterone replacement therapy resulted in structural impairments in both female and male offspring. Structural impairments observed in females included increased anogenital distance, phallus development, empty scrotum, no external vagina, intrauterine growth retardation, reduced ovarian reserve, and increased ovarian follicular recruitment. Structural impairments seen in male offspring included increased testicular weight, larger seminal tubular lumen diameter, and higher frequency of occluded tubule lumen. Increased pituitary weight was seen in both sexes.
Testosterone exposure in utero also resulted in hormonal and behavioral changes in offspring. Hypertension was observed in pregnant female rats and their offspring exposed to doses approximately twice those used for testosterone replacement therapy.
During treatment with large doses of exogenous androgens, including KYZATREX™, spermatogenesis may be suppressed through feedback inhibition of the hypothalamicpituitary-testicular axis [see Warnings and Precautions (5.8) and Impairment of Fertility (13.1)] , possibly leading to adverse effects on semen parameters including sperm count. Reduced fertility has been observed in some men taking testosterone replacement therapy. Testicular atrophy, subfertility, and infertility have also been reported in men who abuse anabolic androgenic steroids [see Drug Abuse and Dependence (9.2)]. With either type of use, the impact on fertility may be irreversible.
The safety and efficacy of KYZATREX™ in pediatric patients less than 18 years old have not been established. KYZATREX™ is not recommended for use in patients less than 18 years of age because of the potential for acceleration of bone age and premature closure of epiphyses.
Clinical studies of KYZATREX™ did not include any patients 65 years of age and older. Therefore, it cannot be determined whether these patients respond differently from younger adult patients. Additionally, there are insufficient long-term safety data in geriatric patients to assess the potentially increased risk of cardiovascular disease and prostate cancer.
Geriatric patients treated with androgens including KYZATREX™ may be at risk for worsening of signs and symptoms of BPH [see Warnings and Precautions (5.4)] .
KYZATREX™ contains testosterone undecanoate, a Schedule III controlled substance
Drug abuse is intentional non-therapeutic use of a drug, even once, for its rewarding psychological and physiological effects. Abuse and misuse of testosterone are seen in male and female adults and adolescents. Testosterone, often in combination with other anabolic androgenic steroids, and not obtained by prescription through a pharmacy, may be abused by athletes and bodybuilders. There have been reports of misuse by men taking higher doses of legally obtained testosterone than prescribed and continuing testosterone despite adverse events or against medical advice.
Abuse-Related Adverse Reactions
Serious adverse reactions have been reported in individuals who abuse anabolic androgenic steroids and include cardiac arrest, myocardial infarction, hypertrophic cardiomyopathy, congestive heart failure, cerebrovascular accident, hepatotoxicity, and serious psychiatric manifestations, including major depression, mania, paranoia, psychosis, delusions, hallucinations, hostility, and aggression.
The following adverse reactions have also been reported in men: transient ischemic attacks, convulsions, hypomania, irritability, dyslipidemias, testicular atrophy, subfertility, and infertility.
The following additional adverse reactions have been reported in women: hirsutism, virilization, deepening of voice, clitoral enlargement, breast atrophy, male-pattern baldness, and menstrual irregularities. The following adverse reactions have been reported in male and female adolescents: premature closure of bony epiphyses with termination of growth, and precocious puberty.
Because these reactions are reported voluntarily from a population of uncertain size and may include abuse of other agents, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure.
Behaviors Associated with Addiction
Continued abuse of testosterone and other anabolic steroids leading to addiction is characterized by the following behaviors:
Physical dependence is characterized by withdrawal symptoms after abrupt drug discontinuation or a significant dose reduction of a drug. Individuals taking supratherapeutic doses of testosterone may experience withdrawal symptoms lasting for weeks or months, which may include depressed mood, major depression, fatigue, craving, restlessness, irritability, anorexia, insomnia, decreased libido, and hypogonadotropic hypogonadism.
Drug dependence in individuals using approved doses of testosterone for approved indications has not been documented.
There is one report of acute overdosage with use of an approved injectable testosterone product: this subject had serum testosterone levels of up to 11,400 ng/dL with a cerebrovascular accident.
Treatment of overdosage consists of discontinuation of KYZATREX™ and appropriate symptomatic and supportive care.
KYZATREX™ is provided as a gelatin capsule containing testosterone undecanoate, a fatty-acid ester of testosterone. Testosterone undecanoate is a white to off-white yellow crystalline powder. Testosterone, an androgen, is formed by cleavage of the ester side chain of testosterone undecanoate.
Testosterone undecanoate is chemically described as 17β-hydroxyandrost-4-en-3-one undecanoate. It has the empirical formula of C 30H 48O 3 and a molecular weight of 456.7 g/mol. The structural formula for testosterone undecanoate is presented in Figure 1.
KYZATREX™ (testosterone undecanoate) capsules for oral use are available in three dosage strengths- 100 mg, 150 mg, and 200 mg. The 100 mg strength is an opaque, white capsule imprinted with "MP100" in red ink. The 150 mg strength is an opaque white capsule imprinted with "MP150" in red ink. The 200 mg strength is an opaque white capsule imprinted with "MP200" in red ink. All capsule strengths also contain DL-alpha-tocopheryl acetate (Vitamin E), phytosterol esters, polyoxyl 40 hydrogenated castor oil, and propylene glycol monolaurate as inactive ingredients.
Gelatin capsule shells are composed of the following inactive ingredients: gelatin, glycerin, purified water, sorbitol, and titanium dioxide.
Endogenous androgens, including testosterone and dihydrotestosterone (DHT), are responsible for the normal growth and development of the male sex organs and for maintenance of secondary sex characteristics. These effects include the growth and maturation of prostate, seminal vesicles, penis, and scrotum; the development of male hair distribution, such as facial, pubic, chest, and axillary hair; laryngeal enlargement; vocal cord thickening; alterations in body musculature; and fat distribution.
Male hypogonadism, a clinical syndrome resulting from insufficient secretion of testosterone, has two main etiologies. Primary hypogonadism is caused by defects of the gonads, such as Klinefelter syndrome or Leydig cell aplasia, whereas secondary hypogonadism (also known as hypogonadotropic hypogonadism) is the failure of the hypothalamus (or pituitary gland) to produce sufficient gonadotropins (FSH, LH).
There is insufficient data to characterize an exposure-response relationship or time course of pharmacodynamics.
KYZATREX™ was taken orally at a starting dose of 200 mg twice per day with meals in a multicenter, open-label trial in hypogonadal males. The dose was adjusted, as needed, on Days 28 and 56 from a minimum dose of 100 mg (morning-only) to a maximum dose of 400 mg twice per day based on the plasma testosterone concentration obtained by a single blood draw collected 3 to 5 hours after the morning dose. The average daily NaF/EDTA plasma testosterone concentration was 393.3 (±113.6) ng/dL after 90 days of treatment (normal eugonadal range in NaF/EDTA plasma: 222-800 ng/dL. Note that the titration scheme for use in clinical practice is based on serum total testosterone [see Dosage and Administration (2.2)] .
KYZATREX™ is expected to produce testosterone concentrations that approximate normal concentrations seen in healthy men.
Table 5 summarizes the pharmacokinetic (PK) parameters for plasma total testosterone in patients completing at least 90 days of KYZATREX™ treatment administered daily.
|PK Parameter||Plasma (N=130)|
|PK = pharmacokinetic; C avg = 24-hour average concentration; C max = maximum concentration|
|C avg (ng/dL)||n||127|
|C max (ng/dL)||n||130|
Figure 2 summarizes the mean plasma total testosterone profile at the final PK visit.
|SEM = standard error of the mean
Testosterone normal ranges: plasma = 222-800 ng/dL
When KYZATREX™ was given with breakfast containing 16%, 33%, and 45% fat, the exposure (AUC 0-24 hr) of testosterone was increased by 37%, 87%, and 94%, respectively, compared to when given under fasted conditions. The primary efficacy and safety study was conducted under fed conditions regardless of the type of meals and the primary efficacy endpoint of achieving testosterone C avg in normal testosterone range was met.
There was no effect on testosterone PK when KYZATREX™ was administered with 20% alcohol along with a high-fat meal versus a high-fat meal alone.
Circulating testosterone is primarily bound in serum to sex hormone-binding globulin (SHBG) and albumin. Approximately 40% of testosterone in plasma is bound to SHBG, 2% remains unbound (free), and the rest is loosely bound to albumin and other proteins.
The androgenic activity of testosterone undecanoate occurs after the ester bond linking the testosterone to the undecanoic acid is cleaved by endogenous non-specific esterases.
Undecanoic acid is metabolized like all fatty acids via the beta-oxidation pathway.
Testosterone is metabolized to various 17-keto steroids through two different pathways. The major active metabolites of testosterone are dihydrotestosterone (DHT) and estradiol.
About 90% of a dose of testosterone given intramuscularly is excreted in the urine as glucuronic and sulfuric acid conjugates of testosterone and its metabolites. About 6% of a dose is excreted in the feces, mostly in the unconjugated form. Inactivation of testosterone occurs primarily in the liver.
Testosterone has been tested by subcutaneous injection and implantation in mice and rats. In mice, the implant induced cervical-uterine tumors, which metastasized in some cases. There is suggestive evidence that injection of testosterone into some strains of female mice increases their susceptibility to hepatoma. Testosterone is also known to increase the number of tumors and decrease the degree of differentiation of chemically induced carcinomas of the liver in rats.
Testosterone was negative in the in vitro Ames and in the in vivo mouse micronucleus assays.
Impairment of Fertility
The administration of exogenous testosterone suppressed spermatogenesis and impaired fertility in the rat, dog, and non-human primate, which was reversible on cessation of treatment.
A reproductive toxicology study was conducted in rats to evaluate functional effects of KYZATREX™ on male fertility. In untreated female rats mated with males receiving 2 times the maximum recommended human daily dose (MRHDD) of KYZATREX™ (based on mean AUC exposure to testosterone), the number of impregnated females was reduced, fertility was significantly lower, and pre-implantation loss was significantly higher compared to the control group. There was no impairment of fertility in males receiving an equivalent dose of KYZATREX™ to the MRHDD.
A 3-month repeat-dose oral toxicity study in male eugonadal dogs was conducted to evaluate whether phytosterol esters present in the KYZATREX™ formulation influenced target organ toxicity due to their structural similarities to sex steroids like testosterone. KYZATREX™ doses 2 times the MRHDD (based on mean AUC exposure to testosterone) produced similar effects on androgen-responsive tissues as testosterone undecanoate without phytosterol esters. These included mild to marked effects on the testes (decreased size, germ cell depletion, Leydig cell atrophy), epididymides (aspermia), adrenal glands (vacuolation in the zona fasciculata) and prostate (increased size and glandular hypertrophy/hyperplasia). Following a 4-week treatment-free period, findings in the testes, epididymides, and adrenal glands were not fully reversible at doses of 2 times the MRHDD of KYZATREX™ as compared to treatment with the excipients alone, including phytosterol esters. Reversibility was not assessed in testosterone undecanoate groups without phytosterol esters.
The efficacy and safety of KYZATREX™ were evaluated in Study MRS-TU-2019EXT (NCT04467697) a multi-center, open-label study of approximately 6 months of duration in 155 hypogonadal males.
Patients received KYZATREX™ at a starting dose of 200 mg twice daily with meals. The dosage was adjusted on Days 28 and 56 between a minimum dose of 100 mg (single morning dose) and a maximum dose of 800 mg (400 mg twice daily) based on plasma testosterone concentration from a single blood draw between 3 to 5 hours after the morning dose.
The primary efficacy endpoint was the percentage of KYZATREX™-treated patients with mean plasma total testosterone concentration (C avg) over 24-hours within the normal range of 222-800 ng/dL on the final PK visit of the study at Day 90.
The efficacy population consisted of 139 hypogonadal, males with a median age of 50 years (range 22 to 66 years), 79% were White, 16% were Black, 3% were Asian, and 2% were American Indian, Alaskan Native or Other.
Primary efficacy results are summarized in Table 6.
|C avg = 24-hour average concentration|
|Patients (%) with Testosterone, C avg (ng/dL), 222-800 ng/dL||122 (88%)|
|95% Confidence Interval||(82%, 93%)|
Secondary endpoints were the percentage of patients with a maximum total testosterone concentration (C max) meeting three predetermined limits: less than or equal to 1.5 times the upper limit of normal range (ULN) (1200 ng/dL), between 1.8 and 2.5 times ULN (1440-2000 ng/dL), and greater than 2.5 times ULN (2000 ng/dL).
The percentage of patients who received KYZATREX™ and had testosterone Cmax threshold less than or equal to 1200 ng/dL, between 1440 and 2000 ng/dL, and greater than 2000 ng/dL at the final PK visit were 88%, 4%, and 0%, respectively.
KYZATREX™ capsules are available in three strengths of 100 mg, 150 mg, and 200 mg packaged as 90 and 120 units in wide-mouth, round, white HDPE bottles with white, polypropylene, child resistant caps and induction-sealed liner.
Store at 20°C to 25°C (68°F to 77°F), with excursions permitted between 15°C to 30°C (59°F to 86°F) [see USP Controlled Room Temperature]. Store the capsules in a dry place avoiding exposure to excessive moisture and humid conditions.
Dispose of unused KYZATREX™ via a take-back option. If a take-back option is unavailable, follow FDA instructions at www.fda.gov/drugdisposal.
Advise the patient to read the FDA-approved patient labeling (Medication Guide).
Increase in Blood Pressure and Cardiovascular Risk
Advise patients that KYZATREX™ can cause an increase in hemoglobin/hematocrit levels that may increase the risk of thromboembolic events. Advise patients about the importance of completing laboratory testing as instructed by their health care provider while on KYZATREX™ [see Warnings and Precautions (5.2)].
Worsening of Benign Prostatic Hyperplasia (BPH) and Potential Risk of Prostate Cancer
Advise patients that KYZATREX™ can cause increased symptoms of BPH and can increase the risk for prostate cancer. Advise patients to contact their health care provider if they have any prostate-related symptoms [see Warnings and Precautions (5.4)].
Advise patients that KYZATREX™ can cause edema in patients with preexisting cardiac, renal, or hepatic disease. Advise patients to notify their health care provider if edema develops or worsens [see Warnings and Precautions (5.10)].
Advise patients that KYZATREX™ can worsen sleep apnea especially in patients with risk factors such as obesity or chronic lung diseases ™ [see Warnings and Precautions (5.11)].
Advise patients that KYZATREX™ can cause gynecomastia [see Warnings and Precautions (5.12)].
Advise patients to take KYZATREX™ with food [see Dosage and Administration (2.3)].
capsules, for oral use
|This Medication Guide has been approved by the U.S. Food and Drug Administration|
KYZATREX ™ (ky-ZAH-treks)
(testosterone undecanoate) capsules, for oral use, CIII
|What is the most important information I should know about KYZATREX™? KYZATREX™ can cause serious side effects, including:
|What is KYZATREX™
|Do not take KYZATREX™
|Before you take KYZATREX™, tell your healthcare provider about all of your medical conditions, including if you:
Especially, tell your healthcare provider if you take:
|How should I take KYZATREX™
|What are the possible side effects of KYZATREX™
KYZATREX™ may cause serious side effects including:
The most common side effect of KYZATREX™ is high blood pressure.
Other side effects may include headache, joint or back pain, diarrhea, increased red blood cell count, anxiety, constipation, swelling of the legs, and increased prostate specific antigen (PSA) levels.
Tell your healthcare provider if you have any side effect that bothers you or that does not go away.
These are not all the possible side effects of KYZATREX™. For more information, ask your healthcare provider or pharmacist.
Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.
|How should I store KYZATREX™
How should I throw away (dispose of) KYZATREX™ ?
|General information about the safe and effective use of KYZATREX™
Medicines are sometimes prescribed for purposes other than those listed in a Medication Guide. Do not use KYZATREX™ for a condition for which it was not prescribed. Do not give KYZATREX™ to other people, even if they have the same symptoms you have. It may harm them. You can ask your pharmacist or healthcare provider for information about KYZATREX™ that is written for health professionals.
|What are the ingredients in KYZATREX™
Active ingredient: testosterone undecanoate
Inactive ingredients: DL-alpha-tocopheryl acetate (Vitamin E), phytosterol esters, polyoxyl 40 hydrogenated castor oil and propylene glycol monolaurate. The ingredients of the gelatin capsule shells are gelatin, glycerin, purified water, sorbitol, and titanium dioxide.
Raleigh, NC 27615
For more information, go to www.KYZATREX.com or call 1-833-949-5040
testosterone undecanoate capsule, liquid filled
testosterone undecanoate capsule, liquid filled
testosterone undecanoate capsule, liquid filled
|Labeler - Marius Pharmaceuticals (080572348)|
|Procaps S A||880090568||manufacture(80603-101, 80603-103, 80603-105)|
Registration | Serial
88826033 not registered Live/Pending
Marius Pharmaceuticals LLC