Clinical data | |
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Trade names | Megace, others |
Other names | MGA; BDH-1298; NSC-71423; SC-10363; 17α-Acetoxy-6-dehydro-6-methylprogesterone; 17α-Acetoxy-6-methylpregna-4,6-diene-3,20-dione |
License data | |
Routes of administration | By mouth |
Drug class | Progestogen; Progestin; Progestogen ester; Antigonadotropin; Steroidal antiandrogen |
ATC code | |
Legal status | |
Legal status | |
Pharmacokinetic data | |
Bioavailability | 100% [2] |
Protein binding | 82% to albumin, [3] no affinity for SHBG or CBG [2] [4] |
Metabolism | Liver (hydroxylation, reduction, conjugation) [5] |
Elimination half-life | Mean: 34 hours [6] Range: 13–105 hours [6] |
Excretion | Urine: 57–78% [5] Feces: 8–30% [5] |
Identifiers | |
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CAS Number | |
PubChem CID | |
DrugBank | |
ChemSpider | |
UNII | |
KEGG | |
ChEBI | |
CompTox Dashboard (EPA) | |
ECHA InfoCard | 100.008.969 |
Chemical and physical data | |
Formula | C24H32O4 |
Molar mass | 384.516 g·mol−1 |
3D model (JSmol) | |
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Megestrol acetate (MGA), sold under the brand name Megace among others, is a progestin medication which is used mainly as an appetite stimulant to treat wasting syndromes such as cachexia. [2] [6] [7] [1] It is also used to treat breast cancer and endometrial cancer, and has been used in birth control. [6] [7] [8] [9] Megestrol acetate is generally formulated alone, although it has been combined with estrogens in birth control formulations. [10] It is usually taken by mouth. [2]
Side effects of megestrol acetate include increased appetite, weight gain, vaginal bleeding, nausea, edema, low sex hormone levels, sexual dysfunction, osteoporosis, cardiovascular complications, glucocorticoid effects, and others. [7] Megestrol acetate is a progestin, or a synthetic progestogen, and hence is an agonist of the progesterone receptor, the biological target of progestogens like progesterone. [2] It has weak partial androgenic activity, weak glucocorticoid activity, and no other important hormonal activity. [2] Due to its progestogenic activity, megestrol acetate has antigonadotropic effects. [7] The mechanism of action of the appetite stimulant effects of megestrol acetate is unknown. [11] [12] [13]
Megestrol acetate was discovered in 1959 and was introduced for medical use, specifically in birth control pills, in 1963. [8] [9] [14] It may be considered a "first-generation" progestin. [15] The medication was withdrawn in some countries in 1970 due to concerns about mammary toxicity observed in dogs, but this turned out not to apply to humans. [16] [17] [18] [19] [20] Megestrol acetate was approved for the treatment of endometrial cancer in 1971 and wasting syndromes in 1993. [7] [21] It is marketed widely throughout the world. [22] [23] It is available as a generic medication. [24]
Megestrol acetate is used mainly as an appetite stimulant to promote weight gain in a variety of situations. [25] [26] [27] When given at very high dosages, it can substantially increase appetite in most individuals, even those with advanced cancer, and is often used to boost appetite and induce weight gain in patients with cancer or HIV/AIDS-associated cachexia. [25] In addition to its effects on appetite, megestrol acetate appears to have antiemetic effects. [28] [29] Megestrol acetate is also used as an antineoplastic agent in the treatment of breast cancer and endometrial cancer. [25] [30] It is significantly inferior to aromatase inhibitors in both clinical effectiveness and tolerability as a second-line therapy for breast cancer after tamoxifen failure. [31] Megestrol acetate was formerly used in combined oral contraceptives in combination with ethinylestradiol or mestranol, [8] [9] [32] and has been used in a combined injectable contraceptive in combination with estradiol as well. [33]
Although it has not been approved for these uses, megestrol acetate has been studied and/or used off-label for a variety of indications including menopausal hormone therapy [34] [35] [36] and the treatment of hot flashes, [37] [38] [39] [40] gynecological/menstrual disorders, [41] [42] endometriosis, [43] endometrial hyperplasia, [44] ovarian cancer, [45] [46] [47] [48] prostate cancer, [49] [50] [51] [52] [53] [54] [55] benign prostatic hyperplasia, [56] [57] male breast cancer, [58] and precocious puberty. [5] [7] [59] Megestrol acetate can also be used to treat pattern hair loss in men, but its side effects generally make it unacceptable for this purpose. [60]
Appetite stimulation is achieved with megestrol acetate with oral dosages of 400 to 800 mg/day. [61] The optimal dosage with maximum effect for appetite stimulation has been determined to be 800 mg/day. [62]
Megestrol acetate is available as 5 mg, 20 mg, and 40 mg oral tablets and in oral suspensions of 40 mg/mL, 125 mg/mL, 625 mg/5 mL, and 820 mg/20 mL. [61] [63] It was used at doses of 1 mg, 2 mg, 4 mg, and 5 mg in combined oral contraceptives. [8] [9] [32] [33] Megestrol acetate is formulated at a dose of 25 mg in combination with a dose of 3.75 mg estradiol in a microcrystalline aqueous suspension for use as a once-monthly combined injectable contraceptive in women. [33]
Contraindications of megestrol acetate include hypersensitivity to megestrol acetate or any component of its formulation, known or suspected pregnancy, and breastfeeding. [1] Megestrol acetate is a teratogen in animals and may have the potential to cause fetal harm, such as decreased fetal weight and feminization of male fetuses. [1]
The most common side effect of megestrol acetate is weight gain, with an incidence of 15–70% at the high dosages used to treat breast cancer. [6] [5] Other side effects include vaginal bleeding (7–8%), nausea (7%), and edema (5%), as well as others such as dizziness and shortness of breath. [6] [5] [64] Megestrol acetate can cause hypogonadism and associated symptoms like diminished secondary sexual characteristics, sexual dysfunction, osteoporosis, and reversible infertility in men and premenopausal women. [65] [66] [67] Combining megestrol acetate with an androgen/anabolic steroid like oxandrolone, nandrolone decanoate, or testosterone in men can alleviate megestrol acetate-associated symptoms of hypoandrogenism as well as further increase appetite and weight gain. [66] [68] [69] [70] Less common but more serious side effects of megestrol acetate include cardiovascular/thromboembolic complications such as thrombophlebitis. [6] It may also cause glucocorticoid side effects such as Cushing syndrome-like symptoms, steroid diabetes, and adrenal insufficiency at high dosages. [71] [72] [73] Case reports of deep vein thrombosis, pulmonary embolism, jaundice, intrahepatic cholestasis, and meningiomas in association with high-dosage megestrol acetate have been published. [74] [75] [76] [77] In older patients who take megestrol acetate, one in 23 will have an adverse event leading to death. [78]
Megestrol acetate has been studied at very high dosages of as much as 1,600 mg/day with no serious adverse effects observed. [1] [79] No clear increase in rate or severity of side effects have been observed up to 1,600 mg/day megestrol acetate except for weight gain, mild increases in blood pressure, and some fluid retention. [79] In post-marketing experience, limited reports of overdose have been received. [1] Signs and symptoms described in these reports have included diarrhea, nausea, abdominal pain, shortness of breath, cough, unsteady gait, listlessness, and chest pain. [1] There is no specific antidote for overdose of megestrol acetate. [1] Treatment should be supportive and based on symptoms. [1] Megestrol acetate has not been assessed for dialyzability. [1] However, due to its low solubility, it is thought that dialysis would not be useful for treating megestrol acetate overdose. [1]
Interactions of megestrol acetate include significantly decreased exposure to indinavir, which may necessitate an increased dosage of the medication. [1] When megestrol acetate is co-administered with zidovudine and rifabutin, there is no significant change in exposure to these medications and no dosage adjustment is necessary. [1]
Megestrol acetate has progestogenic activity, antigonadotropic effects, weak partial androgenic activity, and weak glucocorticoid activity. [2] [4] [80]
Compound | PR | AR | ER | GR | MR | SHBG | CBG |
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Megestrol acetate | 65 | 5 | 0 | 30 | 0 | 0 | 0 |
Notes: Values are percentages (%). Reference ligands (100%) were promegestone for the PR , metribolone for the AR , estradiol for the ER , dexamethasone for the GR , aldosterone for the MR , dihydrotestosterone for SHBG , and cortisol for CBG . Sources: [2] [4] [80] |
Megestrol acetate is a progestogen, or an agonist of the progesterone receptor (PR). [2] [80] [81] It has about 65% of the affinity of promegestone and 130% of the affinity of progesterone for the progesterone receptor. [80] [81] Like other progestogens, megestrol acetate has functional antiestrogenic effects in certain tissues such as the endometrium and has antigonadotropic effects. [2] [25] [82] The total endometrial transformation dose of megestrol acetate is 50 mg per cycle. [82]
Compound | Form | Dose for specific uses (mg) [lower-alpha 3] | DOA [lower-alpha 4] | |||
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TFD [lower-alpha 5] | POICD [lower-alpha 6] | CICD [lower-alpha 7] | ||||
Algestone acetophenide | Oil soln. | - | – | 75–150 | 14–32 d | |
Gestonorone caproate | Oil soln. | 25–50 | – | – | 8–13 d | |
Hydroxyprogest. acetate [lower-alpha 8] | Aq. susp. | 350 | – | – | 9–16 d | |
Hydroxyprogest. caproate | Oil soln. | 250–500 [lower-alpha 9] | – | 250–500 | 5–21 d | |
Medroxyprog. acetate | Aq. susp. | 50–100 | 150 | 25 | 14–50+ d | |
Megestrol acetate | Aq. susp. | - | – | 25 | >14 d | |
Norethisterone enanthate | Oil soln. | 100–200 | 200 | 50 | 11–52 d | |
Progesterone | Oil soln. | 200 [lower-alpha 9] | – | – | 2–6 d | |
Aq. soln. | ? | – | – | 1–2 d | ||
Aq. susp. | 50–200 | – | – | 7–14 d | ||
Notes and sources:
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Megestrol acetate has antigonadotropic effects in humans at sufficient doses, capable of profoundly suppressing circulating androgen and estrogen concentrations. [25] [52] [102] [103] [104] [105] The antigonadotropic effects of megestrol acetate are the result of activation of the progesterone receptor, which suppresses the secretion of the gonadotropins—peptide hormones responsible for signaling the body to produce not only progesterone but also the androgens and the estrogens—from the pituitary gland as a form of negative feedback inhibition, and hence downregulates the hypothalamic–pituitary–gonadal axis (HPG axis), resulting in decreased levels of the sex hormones and interference with fertility. [106] As such, megestrol acetate has functional antiandrogenic and antiestrogenic effects as well as contraceptive effects via its antigonadotropic effects. [7]
The precise ovulation-inhibiting dosage of megestrol acetate is unknown. [82] [107] However, doses of 1 to 5 mg megestrol acetate were previously used in combined birth control pills in combination with the estrogen ethinylestradiol or mestranol. [8] [9] [32] Megestrol acetate is an effective contraceptive by itself at dosages of 0.35 to 0.5 mg/day, but is not effective at a dosage of 0.25 mg/day. [7] Megestrol acetate alone does not inhibit ovulation at a dosage of 0.5 mg/day, nor does it fully inhibit ovulation at a dosage of 0.7 mg/day or even at a dosage of 5 mg/day. [7] [41] [108] The combination of 2 to 5 mg/day megestrol acetate and 100 μg/day mestranol has been found to consistently inhibit ovulation, whereas either medication alone did not completely inhibit ovulation in all women. [41] [109]
Suppression of testosterone levels by megestrol acetate is responsible for its effectiveness in the treatment of conditions like prostate cancer and benign prostatic hyperplasia. [7] [110] In one study, 120 to 160 mg/day megestrol acetate suppressed testosterone levels in men by 72%. [104] However, a recovery or "escape" of testosterone levels, gradually returning to near-normal values, has been observed in most men after 2 to 6 months of megestrol acetate therapy, and this has limited the usefulness of the medication. [25] [111] [112] [113] The combination of a lower dosage of megestrol acetate (40–80 mg/day) and a low oral dosage of an estrogen such as estradiol (0.5–1.5 mg/day), diethylstilbestrol (0.1–0.2 mg/day) or ethinylestradiol (50 µg/day) is able to suppress testosterone levels into the castrate range in men, maintain this suppression long-term, and achieve equivalent effectiveness to high-dosage estrogen monotherapy in the treatment of prostate cancer with comparatively greatly reduced toxicity and side effects. [7] [25] [52] [53] [111] [114] [115] [116] [117] In spite of these results, however, this combination has been very rarely used to treat prostate cancer in the United States. [111]
The antigonadotropic as well as anticorticotropic effects of megestrol acetate may be involved in its effectiveness in the treatment of postmenopausal breast cancer via substantially decreasing gonadal and adrenal production of sex steroids and by extension circulating levels of estrogens, by about 80%. [118] [119] [120]
Megestrol acetate is a weak partial agonist of the androgen receptor (AR). [121] [122] [123] It has been reported to bind to this receptor with 5% of the affinity of the anabolic steroid metribolone. [2] [4] [80] Despite its weak intrinsic activity at the androgen receptor, at clinical doses in humans, megestrol acetate appears to behave, for all intents and purposes, purely as an antiandrogen. [124] This is based on the fact that no virilizing side effects have been observed with the use of megestrol acetate in patients of either sex at dosages up to as high as 1,600 mg per day, the highest that has been assessed. [124] Furthermore, megestrol acetate produces detectable androgenic effects in animals only at a dose that is the equivalent of approximately 200 times that typically used for the treatment of prostate cancer in men. [125] However, the medication does have moderate androgenic effects on serum lipids in humans, causing a significant reduction of HDL and LDL cholesterol levels and no change in triglyceride levels at a dosage of only 5 mg/day. [2] Conversely, megestrol acetate does not decrease sex hormone-binding globulin levels. [126] The weak but significant androgenic activity of megestrol acetate may serve to limit its clinical effectiveness in the treatment of prostate cancer. [122] [123] [127] [128]
Megestrol acetate is an agonist of the glucocorticoid receptor (GR), the biological target of glucocorticoids like cortisol. [2] [4] [80] It has been found to possess 30% of the affinity of the corticosteroid dexamethasone for this receptor. [2] [4] [80] Megestrol acetate shows the lowest ratio of progesterone receptor affinity to glucocorticoid receptor affinity of a broad selection of marketed progestins, suggesting that it may have among the highest relative glucocorticoid effect of the progestins used in medicine. [2] Megestrol acetate produces observable glucocorticoid effects, with one study finding that, in the dose range tested, it possessed about 50% of the eosinopenic and hyperglycemic activity (markers of glucocorticoid activity) of an equal amount of medroxyprogesterone acetate and about 25% that of hydrocortisone. [129] Accordingly, manifestations of its glucocorticoid activity, including symptoms of Cushing's syndrome, steroid diabetes, and adrenal insufficiency, have been reported with the use of megestrol acetate in the literature, albeit sporadically. [71]
Megestrol acetate is frequently used as an appetite stimulant to promote weight gain. [25] [26] [27] The direct mechanism of appetite enhancement is unclear, but it is known that megestrol acetate induces a variety of downstream changes to cause the effect, including stimulation of the release of neuropeptide Y in the hypothalamus, neurosteroid-like modulation of calcium channels in the ventromedial hypothalamus, [130] and inhibition of the secretion of proinflammatory cytokines including interleukin 1α, interleukin 1β, interleukin 6, and tumor necrosis factor α, all of which have been implicated in facilitation of appetite. [11] [12] [13] Increased levels of insulin-like growth factor 1 (IGF-1) may also be involved, specifically in its anabolic effects. [131] Studies of megestrol acetate in elderly patients who experience weight loss are limited and of poor quality with most showing minimal or no weight gain, with no nutritional or clinically significant beneficial outcomes observed. In patients who take megestrol acetate, one in 12 will have an increase in weight. [78]
Unlike the case of the androgen receptor, megestrol acetate has no significant affinity for the estrogen receptor. [2] [4] [80] As such, it does not possess the capacity to directly activate the estrogen receptor. [2] [4] [80] Furthermore, unlike antiandrogens such as spironolactone and bicalutamide but similarly to cyproterone acetate, there is relatively little risk of indirectly mediated estrogenic side effects (e.g., gynecomastia) with megestrol acetate. [132] This is because megestrol acetate strongly suppresses both androgen and estrogen levels at the same time. [25] [52] [102] [103] [104] [105] Similarly to the case of the estrogen receptor, megestrol acetate has negligible affinity for the mineralocorticoid receptor (MR), and hence does not possess mineralocorticoid or antimineralocorticoid activity. [2] [4] [80]
Megestrol acetate has been found to dose-dependently increase total and free IGF-1 levels up to a dosage of 120 mg/day. [131] Total IGF-1 levels were described as "profoundly" increased, gradually increasing, significantly by 3 days of treatment, up to a maximum of 2.66-fold by 5 to 6 months of treatment. [131] Free (readily dissociable) concentrations of IGF-1 were increased to a smaller extent, by 1.23–2.15-fold, and were described as increasing "moderately". [131] It was suggested that the increase in IGF-1 levels with high-dosage megestrol acetate therapy may explain the anabolic effects of megestrol acetate in patients with cachexia. [131]
The oral bioavailability of megestrol acetate is approximately 100%. [2] After a single low oral dose of 4 mg megestrol acetate, peak serum concentrations of megestrol acetate were about 7 ng/dL (18 nmol/L) and occurred after 3 hours. [2] Following a single high oral dose of 160 mg micronized megestrol acetate in men, peak circulating levels of megestrol acetate were 125 ng/mL (325 nmol/L) and occurred after 6.3 hours. [133] [134] [135] This study found that micronized megestrol acetate at this dose showed considerably improved absorption relative to its conventional tablet form. [133] [134] [135] In terms of plasma protein binding, megestrol acetate is bound mostly to albumin (82.4%) and is not bound to sex hormone-binding globulin or to corticosteroid-binding globulin. [2] [3] [4] Megestrol acetate metabolized in the liver mainly by hydroxylation of the C21, C2α, and C6 positions, as well as by reduction and conjugation. [2] [5] Its elimination half-life is 34 hours on average, with a range of 13 to 105 hours. [6] Megestrol acetate is excreted 57 to 78% in urine and 8 to 30% in feces. [5]
At high doses, megestrol acetate appears to have far greater bioavailability and potency than medroxyprogesterone acetate, regardless of whether the route of administration of the latter is oral or parenteral. [5] [136] [137] Following oral administration of 80 to 160 mg megestrol acetate or 500 to 1,000 mg medroxyprogesterone acetate, circulating levels of megestrol acetate were 2- to 10-fold higher than those of medroxyprogesterone acetate. [5] [136] [137] Similar findings have been found for oral megestrol acetate relative to medroxyprogesterone acetate administered via intramuscular injection. [5] Megestrol acetate also reaches steady-state levels more quickly than medroxyprogesterone acetate. [137] The improved potency of megestrol acetate compared to medroxyprogesterone acetate may be due to increased resistance to metabolism of megestrol acetate afforded by its C6(7) double bond (medroxyprogesterone acetate being identical to megestrol acetate in structure except lacking this feature). [5] [138] [139]
The pharmacokinetics of megestrol acetate have been reviewed. [2] [82] [140]
Megestrol acetate, also known as 17α-acetoxy-6-dehydro-6-methylprogesterone or as 17α-acetoxy-6-methylpregna-4,6-diene-3,20-dione, is a synthetic pregnane steroid and a derivative of progesterone. [22] [141] It is specifically a derivative of 17α-hydroxyprogesterone with a methyl group at the C6 position, a double bond between the C6 and C7 positions, and an acetate ester at the C17α position. [22] [141] Megestrol acetate is the C17α acetate ester of megestrol, which, in contrast to megestrol acetate, was never marketed. [22] [141] Analogues of megestrol acetate include other 17α-hydroxyprogesterone derivatives such as acetomepregenol, anagestone acetate, chlormadinone acetate, cyproterone acetate, hydroxyprogesterone caproate, medroxyprogesterone acetate, and nomegestrol acetate. [22] [141] Megestrol acetate differs from medroxyprogesterone acetate only by its C6(7) double bond. [142] Close analogues of megestrol acetate that were never marketed include cymegesolate (megestrol acetate 3β-cypionate) and megestrol caproate. [143] [144] [145]
Chemical syntheses of megestrol acetate have been published. [146] [147]
Megestrol acetate was synthesized at Syntex in 1959. [82] It was derived from medroxyprogesterone acetate, which had been synthesized at Syntex in 1957. [14] [82] Megestrol acetate was the third synthetic derivative of progesterone to be developed for use as a medication, following hydroxyprogesterone caproate in 1954 and medroxyprogesterone acetate in 1957. [82] The medication was introduced for medical use in combination with ethinylestradiol (EE) as an oral contraceptive in 1963 by British Drug Houses in the United Kingdom under the brand name Volidan (4 mg MGA and 50 μg EE tablets), [8] [9] and this was followed by Serial 28 (1 mg MGA and 100 μg EE tablets) and Volidan 21 (4 mg MGA and 50 μg EE tablets) in 1964 and Nuvacon (2 mg MGA and 100 μg EE tablets) in 1967, all by British Drug Houses also in the United Kingdom. [32] It was also marketed under the brand name Delpregnin (5 mg MGA and 100 μg mestranol tablets) by 1965, among others. [136] [148] [149] [150] Megestrol acetate-containing birth control pills were withdrawn after reports in the early 1970s of a high incidence of venous thromboembolism with the preparations. [126]
In the early 1970s, megestrol acetate was found to be associated with mammary tumors in beagle dogs, and along with several other progestogens, was withdrawn as an oral contraceptive from several markets including the United Kingdom, Canada, and West Germany. [16] [17] [18] It was also under investigation for use as a contraceptive in the United States, but development was discontinued in 1972 following the mammary toxicity findings in dogs, and megestrol acetate was never marketed as an oral contraceptive in the United States. [18] [19] [151] Subsequent research, such as monkey studies, revealed that there is no similar risk in humans. [5] [20] Following its withdrawal from the market, megestrol acetate was eventually reintroduced for the treatment of hormone-sensitive cancers. [151] In addition, megestrol acetate was marketed for veterinary use in dogs in 1969 in the United Kingdom and in 1974 in the United States. [152] [153] [154]
Progesterone was first found to be effective in the treatment of endometrial hyperplasia in 1951, [5] and progestins were first found to be effective in the treatment of endometrial cancer in 1959. [155] Megestrol acetate was reported to be effective in the treatment of endometrial hyperplasia in the mid-1960s. [5] It first started to be studied as a treatment for endometrial cancer in 1967, with findings published in 1973. [5] [156] [157] Megestrol acetate was reportedly introduced for the treatment of endometrial cancer in the United States in 1971. [7] Progesterone was studied in the treatment of breast cancer in 1951 and 1952, but with relatively modest results. [158] [159] [160] Megestrol acetate was first studied in the treatment of breast cancer in 1967, and was one of the first progestins to be evaluated for the treatment of this disease. [5] [30] [161] A second study was conducted in 1974. [5] [162] A "breakthrough" and surge of interest in progestins for breast cancer occurred in 1978 when a study using a massive dosage of medroxyprogesterone acetate to treat breast cancer was published. [158] [163] A third study of megestrol acetate for breast cancer was published in 1980, and this was followed by additional studies in the 1980s and beyond. [5] [164] [165] Megestrol acetate was approved for the treatment of breast cancer in the United States by at least 1983. [5]
Progestogens, including progesterone and ethisterone, were studied in the treatment prostate cancer in 1949. [5] [166] Megestrol acetate was first studied in the treatment of prostate cancer in 1970. [5] [167] Additional studies were conducted in 1975 and 1978, followed by others thereafter. [5] [7] [50] [54] However, results of megestrol acetate therapy for prostate cancer have been "disappointing", [168] and the medication has not been approved for the treatment of prostate cancer in the United States or elsewhere. [111]
Clinical studies of very high dosages of megestrol acetate for breast cancer conducted in the 1980s observed markedly increased appetite and weight gain in treated patients despite them having advanced cancer. [169] [170] This led to potential interest in megestrol acetate as an appetite stimulant, [169] and in 1986, a paper was published proposing the study and potential use of megestrol acetate in cachexia. [170] [171] [172] Megestrol acetate was subsequently studied for this indication [173] and, following completion of phase III clinical trials, was approved as an oral suspension for the treatment of anorexia–cachexia syndrome due to cancer and other chronic conditions such as HIV/AIDS in the United States in 1993. [21] [174] Thereafter, the branded product, Megace ES, has been heavily promoted by its maker, Par Pharmaceutical, for treatment of unintentional weight loss in elderly patients, especially those living in long-term care facilities. In March 2013, Par settled a $45 million federal and multi-state criminal and civil lawsuit in which the company was accused of promoting the branded version of megestrol acetate, over the generic version, for use in treating non-AIDS-related geriatric wasting. This use was not approved as safe and effective by the Food and Drug Administration (FDA), and not covered by federal health care programs. The lawsuit claimed that Par marketed the product as effective for this use, despite having conducted no well-controlled studies to support a claim of greater efficacy for Megace ES, and prior knowledge of the severe adverse side effects for geriatric patients, including deep vein thrombosis, toxic reactions with impaired renal function, and mortality. [175]
Megestrol acetate is the generic name of the drug and its INNM , USAN , USP , and BANM , while megestrol is the INN and BAN and mégestrol the DCF of megestrol, the free alcohol form of megestrol acetate. [10] [22] [23] [141] The medication is also known by its developmental code names BDH-1298, NSC-71423, and SC-10363. [10] [22] [23] [141]
Megestrol acetate is marketed under a variety of brand names throughout the world but is most commonly sold under the brand name Megace. [22] [23] [141] It is also available under the brand name Megace ES in the United States and under the brand name Megace OS in Canada. [23] For use in veterinary medicine, megestrol acetate is sold as Ovaban in the United States and as Ovarid in the United Kingdom. [23]
In Bangladesh and India, megestrol is marketed under the brand name Megestol by Ziska Pharmaceuticals, Mezest by Beacon Pharmaceuticals, and under the trade name Varigestrol by Laboratorio Varifarma, Argentina.
Megestrol acetate is available widely throughout the world, including in the United States, Canada, the United Kingdom, Ireland, elsewhere throughout Europe, Australia, New Zealand, Latin America, Asia, and a few African countries. [22] [23]
Progestins in birth control pills are sometimes grouped by generation. [176] [177] While the 19-nortestosterone progestins are consistently grouped into generations, the pregnane progestins that are or have been used in birth control pills are typically omitted from such classifications or are grouped simply as "miscellaneous" or "pregnanes". [176] [177] In any case, based on its date of introduction in such formulations of 1963, megestrol acetate could be considered a "first-generation" progestin. [15]
Megestrol acetate has been studied in men in combination with testosterone as a male hormonal contraceptive to suppress spermatogenesis. [7] [178]
Megestrol acetate has been used in veterinary medicine under the brand name Ovaban in the treatment of medical conditions in cats and dogs. [22] [179] Due to its ability to suppress testosterone levels, megestrol acetate can control sexually dimorphic traits in males. [180] [181] As a result, megestrol acetate has been used to reduce dominance, inter-male aggression, mounting, urine spraying, and roaming in male dogs and cats. [180] [181]
A progestogen, also referred to as a progestagen, gestagen, or gestogen, is a type of medication which produces effects similar to those of the natural female sex hormone progesterone in the body. A progestin is a synthetic progestogen. Progestogens are used most commonly in hormonal birth control and menopausal hormone therapy. They can also be used in the treatment of gynecological conditions, to support fertility and pregnancy, to lower sex hormone levels for various purposes, and for other indications. Progestogens are used alone or in combination with estrogens. They are available in a wide variety of formulations and for use by many different routes of administration. Examples of progestogens include natural or bioidentical progesterone as well as progestins such as medroxyprogesterone acetate and norethisterone.
Drospirenone is a progestin and antiandrogen medication which is used in birth control pills to prevent pregnancy and in menopausal hormone therapy, among other uses. It is available both alone under the brand name Slynd and in combination with an estrogen under the brand name Yasmin among others. The medication is an analog of the drug spironolactone. Drospirenone is taken by mouth.
Norethisterone acetate (NETA), also known as norethindrone acetate and sold under the brand name Primolut-Nor among others, is a progestin medication which is used in birth control pills, menopausal hormone therapy, and for the treatment of gynecological disorders. The medication available in low-dose and high-dose formulations and is used alone or in combination with an estrogen. It is ingested orally.
Norethisterone, also known as norethindrone and sold under many brand names, is a progestin medication used in birth control pills, menopausal hormone therapy, and for the treatment of gynecological disorders. The medication is available in both low-dose and high-dose formulations and both alone and in combination with an estrogen. It is used by mouth or, as norethisterone enanthate, by injection into muscle.
Gestonorone caproate, also known as gestronol hexanoate or norhydroxyprogesterone caproate and sold under the brand names Depostat and Primostat, is a progestin medication which is used in the treatment of enlarged prostate and cancer of the endometrium. It is given by injection into muscle typically once a week.
Dydrogesterone, sold under the brand name Duphaston among others, is a progestin medication which is used for a variety of indications, including threatened or recurrent miscarriage during pregnancy, dysfunctional bleeding, infertility due to luteal insufficiency, dysmenorrhea, endometriosis, secondary amenorrhea, irregular cycles, premenstrual syndrome, and as a component of menopausal hormone therapy. It is taken by mouth.
Hydroxyprogesterone caproate, sold under the brand names Proluton and Makena among others, is a medication used to reduce the risk of preterm birth in women pregnant with one baby who have a history of spontaneous preterm birth. In March 2023, the manufacturer, Covis Pharma, agreed to withdraw the drug from the US market. The approvals of Makena and its generics were withdrawn by the US Food and Drug Administration (FDA) in April 2023.
Feminizing hormone therapy, also known as transfeminine hormone therapy, is hormone therapy and sex reassignment therapy to change the secondary sex characteristics of transgender people from masculine or androgynous to feminine. It is a common type of transgender hormone therapy and is used to treat transgender women and non-binary transfeminine individuals. Some, in particular intersex people but also some non-transgender people, take this form of therapy according to their personal needs and preferences.
Combined injectable contraceptives (CICs) are a form of hormonal birth control for women. They consist of monthly injections of combined formulations containing an estrogen and a progestin to prevent pregnancy.
Chlormadinone acetate (CMA), sold under the brand names Belara, Gynorelle, Lutéran, and Prostal among others, is a progestin and antiandrogen medication which is used in birth control pills to prevent pregnancy, as a component of menopausal hormone therapy, in the treatment of gynecological disorders, and in the treatment of androgen-dependent conditions like enlarged prostate and prostate cancer in men and acne and hirsutism in women. It is available both at a low dose in combination with an estrogen in birth control pills and, in a few countries like France and Japan, at low, moderate, and high doses alone for various indications. It is taken by mouth.
Algestone acetophenide, also known more commonly as dihydroxyprogesterone acetophenide (DHPA) and sold under the brand names Perlutal and Topasel among others, is a progestin medication which is used in combination with an estrogen as a form of long-lasting injectable birth control. It has also been used alone, but is no longer available as a standalone medication. DHPA is not active by mouth and is given once a month by injection into muscle.
Medroxyprogesterone acetate (MPA), also known as depot medroxyprogesterone acetate (DMPA) in injectable form and sold under the brand name Depo-Provera among others, is a hormonal medication of the progestin type. It is used as a method of birth control and as a part of menopausal hormone therapy. It is also used to treat endometriosis, abnormal uterine bleeding, paraphilia, and certain types of cancer. The medication is available both alone and in combination with an estrogen. It is taken by mouth, used under the tongue, or by injection into a muscle or fat.
Medrogestone, sold under the brand name Colprone among others, is a progestin medication which has been used in menopausal hormone therapy and in the treatment of gynecological disorders. It is available both alone and in combination with an estrogen. It is taken by mouth.
Nomegestrol acetate (NOMAC), sold under the brand names Lutenyl and Zoely among others, is a progestin medication which is used in birth control pills, menopausal hormone therapy, and for the treatment of gynecological disorders. It is available both alone and in combination with an estrogen. NOMAC is taken by mouth. A birth control implant for placement under the skin was also developed but ultimately was not marketed.
Cyproterone acetate (CPA), sold alone under the brand name Androcur or with ethinylestradiol under the brand names Diane or Diane-35 among others, is an antiandrogen and progestin medication used in the treatment of androgen-dependent conditions such as acne, excessive body hair growth, early puberty, and prostate cancer, as a component of feminizing hormone therapy for transgender women, and in birth control pills. It is formulated and used both alone and in combination with an estrogen. CPA is taken by mouth one to three times per day.
Estradiol (E2) is a medication and naturally occurring steroid hormone. It is an estrogen and is used mainly in menopausal hormone therapy and to treat low sex hormone levels in women. It is also used in hormonal birth control for women, in feminizing hormone therapy for transgender women, and in the treatment of hormone-sensitive cancers like prostate cancer in men and breast cancer in women, among other uses. Estradiol can be taken by mouth, held and dissolved under the tongue, as a gel or patch that is applied to the skin, in through the vagina, by injection into muscle or fat, or through the use of an implant that is placed into fat, among other routes.
Cymegesolate, also known as cypionyl megestrol acetate or as megestrol acetate 3β-cypionate, is a progestin medication which was never marketed. It was developed in China in the late 1970s and early to mid 1980s for use as a hormonal contraceptive. The medication was formulated at a dose of 50–100 mg in combination with a "trace" dose of 0.25–0.5 mg quinestrol as a long-lasting, once-a-month combined oral contraceptive pill. This combination has been studied in 1,213 women across a total of 9,651 menstrual cycles, with contraceptive effectiveness of over 99.13% and "very few side effects." At the high dose, it showed an anovulation rate of only about 60%, and instead mediated its contraceptive effects via a marked anti-implantation effect.
The pharmacology of progesterone, a progestogen medication and naturally occurring steroid hormone, concerns its pharmacodynamics, pharmacokinetics, and various routes of administration.
The pharmacology of cyproterone acetate (CPA) concerns the pharmacology of the steroidal antiandrogen and progestin medication cyproterone acetate.
The side effects of cyproterone acetate (CPA), a steroidal antiandrogen and progestin, including its frequent and rare side effects, have been studied and characterized. It is generally well-tolerated and has a mild side-effect profile, regardless of dosage, when it used as a progestin or antiandrogen in combination with an estrogen such as ethinylestradiol or estradiol valerate in women. Side effects of CPA include hypogonadism and associated symptoms such as demasculinization, sexual dysfunction, infertility, and osteoporosis; breast changes such as breast tenderness, enlargement, and gynecomastia; emotional changes such as fatigue and depression; and other side effects such as vitamin B12 deficiency, weak glucocorticoid effects, and elevated liver enzymes. Weight gain can occur with CPA when it is used at high doses. Some of the side effects of CPA can be improved or fully prevented if it is combined with an estrogen to prevent estrogen deficiency. Few quantitative data are available on many of the potential side effects of CPA. Pooled tolerability data for CPA is not available in the literature.
A radioimmunoassay (RIA), radioligand assay and equilibrium dialysis for determination of plasma and salivary megestrol acetate (MA) concentration, sex hormone binding globulin (SHBG) capacity in plasma and percentage albumin bound MA were studied in healthy women receiving single im injection of estradiol-megestrol long-acting injectable contraceptive. The results showed that after injection the concentration of plasma MA increased rapidly. The meantime of peak plasma MA level was 3rd day, there was a linear relationship between log of plasma MA concentration and time (day) after administration in all subjects, elimination phase half-life t1/2β = 14.35 ± 9.1 days. The plasma sex hormone-binding globulin capacity significantly increased at 7th, 14th day and decreased at 21st, 29th day after injection. The percentage albumin bound MA was 82.4%. There was no specific sex hormone-binding globulin bound MA. There was a positive correlation between the MA concentrations in saliva and those in plasma.
Several foreign countries, including Germany, Canada, and Great Britain, have banned the sale of birth control pills containing megestrol acetate after a study done at FDA's request indicated it caused breast cancer in dogs. Megestrol acetate has never been marketed in the United States as an oral contraceptive. FDA routinely requires long-term animal studies before any drug can be marketed for human use. Following animal studies with megestrol acetate, FDA in the late sixties and early seventies allowed limited studies of the drug in women. In 1972, after noticing a significant number of test dogs developing breast nodules (none of them malignant), FDA ordered that megestrol acetate be discontinued in human oral contraceptive studies.
Megestrol was never marketed in the United States for contraceptive use because in 1972, FDA took prompt action to discontinue investigational studies on megestrol after dogs exposed to the drug for four years In a chronic toxicity study developed benign breast tumors.
Doses [of megestrol acetate] of as high as 1,600 mg/d, given in divided doses three or four times daily, have been given with no clear increase in side effects except for weight gain, mild increases in blood pressure (BP), and some fluid retention.45
17α-Hydroxyprogesterone caproate is a depot progestogen which is entirely free of side actions. The dose required to induce secretory changes in primed endometrium is about 250 mg. per menstrual cycle.
The results showed that after injection the concentration of plasma MA increased rapidly. The meantime of peak plasma MA level was 3rd day, there was a linear relationship between log of plasma MA concentration and time (day) after administration in all subjects, elimination phase half-life t1/2β = 14.35 ± 9.1 days.
Specific actions of neurosteroids on ion transport across the neuronal plasma membrane have been described (see Fig. 2[10). In hippocampal CA1 neurons, Ffrench Mullen et al. (76) observed an inhibition by PREG, PREGS, and 3α,5β-TH PROG (but not PROG) of both the N- and L-type calcium channel currents, mediated by a pertussis toxin-sensitive G protein mechanism, associated with the activation of protein kinase C. PROG still has no effect on calcium channels of hypothalamic neurons from the ventromedial nucleus; however, the synthetic progestin megestrol acetate inhibits some high-threshold Ca2+ channel currents: not the N-type nor the P-type Ca2+ channel currents, but the residual current. Appetite enhancement induced by megestrol acetate might be partly due to the inhibition of these Ca2+ channel currents, and the attenuation of the firing of ventromedial nucleus neurons, involved in satiety mechanisms (77).
Each Delpregnin tablet contains 5 mg megestrol acetate + 0.1 mg mestranol.
Your Q & A concerning megestrol acetate (Oct MVP, p 27), a product containing this compound (Ovarid: Glaxo) has been commercially available for controlling estrus in bitches in the UK for nearly 2 years.
In England, where megestrol acetate has been marketed for eight years, it is recommended to treat false pregnancy and estrogen-dependent mammary tumors in dogs. It has also been used successfully to treat hypersexuality in male dogs, and miliary dermatitis and eosinophilic granulomas in cats. In 1974, megestrol acetate was approved in the United States for postponement of es- trus and treatment of false pregnancy in dogs.
In 1974, Sobering marketed megestrol acetate3 (Figure 1) under the trade name of Ovaban® (Ovarid® in Europe).