Classifications

• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K31/00—Medicinal preparations containing organic active ingredients
  • A61K31/59—Compounds containing 9, 10- seco- cyclopenta[a]hydrophenanthrene ring systems
  • A61K31/593—9,10-Secocholestane derivatives, e.g. cholecalciferol, i.e. vitamin D3
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K31/00—Medicinal preparations containing organic active ingredients
  • A61K31/59—Compounds containing 9, 10- seco- cyclopenta[a]hydrophenanthrene ring systems
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K31/00—Medicinal preparations containing organic active ingredients
  • A61K31/59—Compounds containing 9, 10- seco- cyclopenta[a]hydrophenanthrene ring systems
  • A61K31/592—9,10-Secoergostane derivatives, e.g. ergocalciferol, i.e. vitamin D2
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K9/00—Medicinal preparations characterised by special physical form
  • A61K9/0012—Galenical forms characterised by the site of application
  • A61K9/0053—Mouth and digestive tract, i.e. intraoral and peroral administration
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K9/00—Medicinal preparations characterised by special physical form
  • A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K9/00—Medicinal preparations characterised by special physical form
  • A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
  • A61K9/4816—Wall or shell material
  • A61K9/4825—Proteins, e.g. gelatin
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P5/00—Drugs for disorders of the endocrine system
  • A61P5/18—Drugs for disorders of the endocrine system of the parathyroid hormones

Definitions

• the disclosure relates generally to Vitamin D repletion and active Vitamin D hormone replacement. More particularly, the disclosure relates to methods of treating elevated blood levels of intact parathyroid hormone (iPTH), such as in secondary hyperparathyroidism, by increasing or maintaining blood concentrations of both 25 -hydroxy vitamin D and 1,25- dihydroxyvitamin D in a patient by administering, as necessary, both Vitamin D repletion and Vitamin D hormone replacement therapies.
• iPTH intact parathyroid hormone
• Secondary hyperparathyroidism is a disorder which develops primarily because of Vitamin D deficiency. It is characterized by abnormally elevated blood levels of parathyroid hormone (PTH) and, in the absence of early detection and treatment, it becomes associated with parathyroid gland hyperplasia and a constellation of metabolic bone diseases. It is a common complication of chronic kidney disease (CKD), with rising incidence as CKD progresses. Secondary hyperparathyroidism can also develop in individuals with healthy kidneys, due to environmental, cultural or dietary factors which prevent adequate Vitamin D supply.
• PTH parathyroid hormone
• CKD chronic kidney disease
• Vitamin D is a term that refers broadly to the organic substances named Vitamin D 2 , Vitamin D 3 , Vitamin D 4 , etc., and to their metabolites and hormonal forms that influence calcium and phosphorus homeostasis.
• Vitamin D deficiency is a term that broadly refers to reduced or low blood levels of Vitamin D, as defined immediately above.
• Vitamin D The most widely recognized forms of Vitamin D are Vitamin D 2 (ergocalciferol) and Vitamin D 3 (cholecalciferol). Vitamin D 2 is produced in plants from ergosterol during sunlight exposure and is present, to a limited extent, in the human diet. Vitamin D 3 is generated from 7- dehydrocholesterol in human skin during exposure to sunlight and also is found, to a greater Atty. Docket No. 31138/43030A PATENT APPLICATION extent than Vitamin D 2 , in the human diet, principally in dairy products (milk and butter), certain fish and fish oils, and egg yolk. Vitamin D supplements for human use consist of either Vitamin D 2 or Vitamin D 3 .
• Vitamin D 2 and Vitamin D 3 are metabolized into prohormones by one or more enzymes located in the liver.
• the involved enzymes are mitochondrial and microsomal cytochrome P450 (CYP) isoforms, including CYP27A1, CYP2R1, CYP3A4, CYP2J3 and possibly others.
• CYP mitochondrial and microsomal cytochrome P450
• These enzymes metabolize Vitamin D 2 into two prohormones known as 25- hydroxy vitamin D 2 and 24(S )-hydroxy vitamin D 2
• Vitamin D 3 into a prohormone known as 25 -hydroxy vitamin D 3 .
• the two 25-hydroxylated prohormones are more prominent in the blood, and are collectively referred to as "25 -hydroxy vitamin D".
• Vitamin D 2 and Vitamin D 3 can be metabolized into these same prohormones outside of the liver in certain epithelial cells, such as enterocytes, which contain the same (or similar) enzymes, but extrahepatic prohormone production probably contributes little to blood levels of 25 -hydroxy vitamin D.
• the rates of hepatic and extrahepatic production of the Vitamin D prohormones are not tightly regulated, and they vary mainly with intracellular concentrations of the precursors (Vitamin D 2 and Vitamin D 3 ). Higher concentrations of either precursor increase prohormone production, while lower concentrations decrease production. Hepatic production of prohormones is inhibited by high levels of 25 -hydroxy vitamin D via a poorly understood mechanism apparently directed to prevention of excessive blood prohormone levels.
• Vitamin D prohormones are further metabolized in the kidneys into potent hormones by an enzyme known as CYP27B1 (or 25 -hydroxy vitamin D 3 -l ⁇ -hydroxylase) located in the proximal kidney tubule.
• the prohormones 25 -hydroxy vitamin D 2 and 24(S)- hydroxyvitamin D 2 are metabolized into hormones known as l ⁇ ,25-dihydroxyvitamin D 2 and l ⁇ ,24(S)-dihydroxyvitamin D 2 .
• 25 -hydroxy vitamin D 3 is metabolized into a hormone known as l ⁇ ,25-dihydroxyvitamin D 3 (or calcitriol). These hormones are released by the kidneys into the blood for systemic delivery.
• Vitamin D prohormones can be metabolized into hormones outside of the kidneys in keratinocytes, lung epithelial cells, enterocytes, cells of the immune system (e.g., macrophages) and certain other cells containing CYP27B1 or similar enzymes, but such Atty. Docket No. 31138/43030A PATENT APPLICATION extrarenal hormone production is incapable of sustaining normal blood levels of 1,25- dihydroxy vitamin D in advanced CKD.
• Blood levels of 1,25-dihydroxyvitamin D are precisely regulated by a feedback mechanism which involves PTH.
• the renal l ⁇ -hydroxylase (or CYP27B1) is stimulated by PTH and inhibited by 1,25-dihydroxyvitamin D.
• VDR Vitamin D receptors
• the secreted PTH stimulates expression of renal CYP27B1 and, thereby, increases production of Vitamin D hormones.
• the parathyroid glands attenuate further PTH secretion.
• renal production of Vitamin D hormones decreases.
• Vitamin D hormone production also directly inhibit further Vitamin D hormone production by CYP27B1.
• PTH secretion can be abnormally suppressed in situations where blood 1,25-dihydroxyvitamin D concentrations become excessively elevated, as can occur in certain disorders or as a result of bolus doses of Vitamin D hormone replacement therapies. Oversuppression of PTH secretion can cause or exacerbate disturbances in calcium homeostasis.
• the parathyroid glands and the renal CYP27B1 are so sensitive to changes in blood concentrations of Vitamin D hormones that serum 1,25- dihydroxyvitamin D is tightly controlled, fluctuating up or down by less than 20% during any 24-hour period. In contrast to renal production of Vitamin D hormones, extrarenal production is not under precise feedback control.
• the Vitamin D hormones have essential roles in human health which are mediated by the intracellular VDR.
• the Vitamin D hormones regulate blood calcium levels by controlling intestinal absorption of dietary calcium and reabsorption of calcium by the kidneys.
• the Vitamin D hormones also participate in the regulation of cellular differentiation and growth and normal bone formation and metabolism. Further, Vitamin D hormones are required for the normal functioning of the musculoskeletal, immune and renin-angiotensin systems. Numerous other roles for Vitamin D hormones are being postulated and elucidated, based on the documented presence of intracellular VDR in nearly every human tissue.
• Vitamin D hormones on specific tissues depend on the degree to which they bind to (or occupy) the intracellular VDR in those tissues.
• the three Vitamin D hormones l ⁇ ,25-dihydroxyvitamin D 2 , l ⁇ ,24(S)-dihydroxyvitamin D 2 , and l ⁇ ,25-dihydroxyvitamin D 3 Atty. Docket No. 31138/43030A PATENT APPLICATION have nearly identical affinities for the VDR and, therefore, have essentially equivalent VDR binding when present at the same intracellular concentrations. VDR binding increases as the intracellular concentrations of the hormones rise, and decreases as the intracellular concentrations fall.
• intracellular concentrations of the Vitamin D hormones change in direct proportion to changes in blood hormone concentrations.
• intracellular concentrations of the Vitamin D hormones also change in direct proportion to changes in blood and/or intracellular prohormone concentrations, as discussed above.
• Vitamin D 2 , Vitamin D 3 and their prohormonal forms have affinities for the VDR which are estimated to be at least 100-fold lower than those of the Vitamin D hormones.
• physiological concentrations of these hormone precursors exert little, if any, biological actions without prior metabolism to Vitamin D hormones.
• Vitamin D 2 and Vitamin D 3 Blood levels of Vitamin D 2 and Vitamin D 3 are normally present at stable, concentrations in human blood, given a sustained, adequate supply of Vitamin D from sunlight exposure and an unsupplemented diet. Slight, if any, increases in blood Vitamin D levels occur after meals since unsupplemented diets have low Vitamin D content, even those containing foods fortified with Vitamin D. The Vitamin D content of the human diet is so low that the National Institutes of Health (NIH) cautions "it can be difficult to obtain enough Vitamin D from natural food sources" [NIH, Office of Dietary Supplements, Dietary Supplement Fact Sheet: Vitamin D (2005)]. Almost all human Vitamin D supply comes from fortified foods, exposure to sunlight or from dietary supplements, with the last source becoming increasingly important.
• NASH National Institutes of Health
• Vitamin D hormone concentrations also remain generally constant through the day in healthy individuals, but can vary significantly over longer periods of time in response to Atty. Docket No. 31138/43030A PATENT APPLICATION seasonal changes in sunlight exposure or sustained alterations in Vitamin D intake. Marked differences in normal Vitamin D hormone levels are commonly observed between healthy individuals, with some individuals having stable concentrations as low as approximately 20 pg/mL and others as high as approximately 70 pg/mL. Due to this wide normal range, medical professionals have difficulty interpreting isolated laboratory determinations of serum total 1,25- dihydroxy vitamin D; a value of 25 pg/mL may represent a normal value for one individual or a relative deficiency in another.
• Transiently low blood levels of 1,25-dihydroxyvitamin D stimulate the parathyroid glands to secrete PTH for brief periods ending when normal blood Vitamin D hormone levels are restored.
• chronically low blood levels of 1,25-dihydroxyvitamin D continuously stimulate the parathyroid glands to secrete PTH, resulting in a disorder known as secondary hyperparathyroidism.
• Chronically low hormone levels also decrease intestinal calcium absorption, leading to reduced blood calcium concentrations (hypocalcemia) which further stimulate PTH secretion.
• Continuously stimulated parathyroid glands become increasingly hyperplastic and eventually develop resistance to regulation by vitamin D hormones. Without early detection and treatment, secondary hyperparathyroidism progressively increases in severity, causing debilitating metabolic bone diseases, including osteoporosis and renal osteodystrophy.
• Kidney Disease Outcomes Quality Initiative (K/DOQI) Clinical Practice Guidelines for Bone Metabolism and Disease in Chronic Kidney Disease [Am. J. Kidney Dis. 42:S1-S2O2, 2003)].
• K/DOQI Guidelines identified the primary etiology of secondary hyperparathyroidism as chronically low blood levels of 1,25-dihydroxyvitamin and recommended regular screening in CKD Stages 3 through 5 for elevated blood PTH levels relative to stage-specific PTH target ranges.
• Stage 3 was defined as moderately decreased kidney function (GFR of 30-59 niL/min/1.73 m 2 ) with an intact PTH (iPTH) target range of 30- 70 pg/mL;
• Stage 4 was defined as severely decreased kidney function (GFR of 15-29 niL/min/1.73 m 2 ), with an iPTH target range of 70-110 pg/mL;
• Stage 5 was defined as kidney failure (GFR of ⁇ 15 niL/min/1.73 m 2 or dialysis) with an iPTH target range of 150-300 pg/mL.
• the Guidelines recommended a follow-up evaluation of serum total 25-hydroxyvitamin D to detect possible Vitamin D insufficiency or deficiency. If 25- hydroxyvitamin D below 30 ng/mL was observed, the recommended intervention was Vitamin D repletion therapy using orally administered ergocalciferol. If 25-hydroxyvitamin D above 30 ng/mL was observed, the recommended intervention was Vitamin D hormone replacement therapy using oral or intravenous Vitamin D hormones or analogues. The Guidelines did not recommend the concurrent application of Vitamin D repletion and Vitamin D hormone Atty. Docket No. 31138/43030A PATENT APPLICATION replacement therapies, consistent with warnings mandated by the Food and Drug Administration in package inserts for Vitamin D hormone replacement products.
• Vitamin D sufficiency as serum 25- hydroxyvitamin D levels > 30 ng/mL.
• Vitamin D They produce pharmacological concentrations of Vitamin D in the lumen of the duodenum which promote catabolism of Vitamin D by 26- hydroxylation in the local enterocytes, causing decreased systemic bioavailability and supraphysiological surges in blood Vitamin D levels. Such surges are undesirable because they promote storage of Vitamin D in adipose tissue, which is less available for later hepatic conversion to 25 -hydroxy vitamin D, and hepatic catabolism of Vitamin D.
• administration of 25- hydroxyvitamin D 3 produced surges or spikes in blood and intracellular 25 -hydroxy vitamin D levels, thereby promoting (a) competitive displacement of Vitamin D hormones from the serum Vitamin D Binding Protein (DBP) and excessive delivery of the displaced hormones to tissues containing VDR, and (b) transiently excessive renal and extrarenal production of Vitamin D hormones, which together led to local and systemic aberrations in calcium and phosphorus metabolism.
• DBP Vitamin D Binding Protein
• Vitamin D therapy is sorely needed, given the problems encountered with the currently available oral Vitamin D supplements and with previously used oral 25 -hydroxy vitamin D 3 .
• Vitamin D repletion and Vitamin D hormone replacement therapies it becomes possible, for the first time, to concurrently apply Vitamin D repletion and Vitamin D hormone replacement therapies in CKD patients who have need of both types of therapies to effectively treat and subsequently prevent secondary hyperparathyroidism.
• the present invention provides a method of increasing or maintaining blood concentrations of both 25 -hydroxy vitamin D and 1,25-dihydroxyvitamin D in a patient by administering, as necessary, both Vitamin D repletion and active Vitamin D hormone replacement therapies.
• the blood concentrations of 25 -hydroxy vitamin D are increased to and maintained at or above 30 ng/mL, and blood concentrations of 1,25-dihydroxyvitamin D are increased to or maintained within a patient's normal historical physiological range for 1,25- dihydroxyvitamin D without causing substantially increased risk of hypercalcemia, hyperphosphatemia or over suppression of plasma iPTH in the patient.
• the blood levels of 25- hydroxyvitamin D are maintained at or above 30 ng/mL between doses of Vitamin D repletion therapies, and the blood levels of 1,25-dihydroxyvitamin D are maintained in the patient's normal historical physiological range between doses of Vitamin D hormone replacement therapies.
• the blood concentration of 25 -hydroxy vitamin D during treatment comprises predominantly 25 -hydroxy vitamin D 3 , with a lesser amount of 25- hydroxyvitamin D 2 .
• the method includes administering predominantly 25-hydroxyvitamin D 3 , with a lesser amount of 25 -hydroxy vitamin D 2 , or solely 25 -hydroxy vitamin D 3 , for 25-hydroxyvitamin D repletion and/or maintenance.
• the invention provides a method of concurrently lowering or maintaining plasma iPTH levels, increasing or maintaining serum calcium levels, maintaining serum phosphorous levels, increasing or maintaining serum 25-hydroxyvitamin D, and increasing or maintaining serum 1,25-dihydroxyvitamin D levels in a human patient by administering to the patient, as necessary, both Vitamin D repletion and Vitamin D hormone replacement therapies.
• the method can further include administration, as necessary, of phosphate binders and/or calcimimetic agents.
• the blood concentration of 25-hydroxyvitamin D during treatment comprises predominantly 25- hydroxyvitamin D 3 , with a lesser amount of 25-hydroxyvitamin D 2 .
• the method includes administering predominantly 25-hydroxyvitamin D 3 , with a lesser amount of 25-hydroxyvitamin D 2 , or solely 25-hydroxyvitamin D 3 , for 25-hydroxyvitamin D repletion and/or maintenance.
• the invention provides a method of reducing the risk of over suppression of plasma iPTH levels in a patient undergoing treatment for elevated levels of Atty. Docket No. 31138/43030A PATENT APPLICATION plasma iPTH, by administering, as necessary, both Vitamin D repletion and Vitamin D hormone replacement therapies in amounts sufficient to decrease elevated plasma iPTH levels while avoiding an abnormally low bone turnover rate.
• the blood concentration of 25-hydroxyvitamin D during treatment comprises predominantly 25- hydroxyvitamin D 3 , with a lesser amount of 25-hydroxyvitamin D 2 .
• the method includes administering predominantly 25-hydroxyvitamin D 3 , with a lesser amount of 25-hydroxyvitamin D 2 , or solely 25-hydroxyvitamin D 3 , for 25-hydroxyvitamin D repletion and/or maintenance.
• Another aspect of the invention is the use of at least one 25-hydroxyvitamin D and at least one active Vitamin D hormone for the preparation of a medicament for the treatment of a condition described herein, such as secondary hyperparathyroidism.
• the 25-hydroxyvitamin D comprises predominantly 25- hydroxyvitamin D 3 , with a lesser amount of 25-hydroxyvitamin D 2 .
• kits for treatment of a condition described herein such as secondary hyperparathyroidism, including a 25-hydroxyvitamin D compound, or an active Vitamin D hormone, or combinations thereof, and written instructions for co-treatment with a 25-hydroxyvitamin D compound and an active Vitamin D hormone.
• kidney osteodystrophy including osteomalacia and osteitis fibrosa cystica.
• the present invention relates to treating and preventing secondary hyperparathyroidism and the underlying chronically low blood levels of 1,25-dihydroxyvitamin D, and various other related abnormalities in mineral and bone metabolism, by administering effective amounts, as necessary, of both Vitamin D repletion and Vitamin D hormone replacement therapies.
• the present invention provides a method of increasing and then maintaining blood concentrations of 25 -hydroxy vitamin D at or above 30 ng/mL, and blood concentrations of 1,25-dihydroxyvitamin D to within a patient's normal historical physiological range for 1,25-dihydroxyvitamin D.
• many conditions can lead to chronically low blood levels of 1,25-dihydroxyvitamin D, including CKD (e.g., Stages 3 and 4, and Stage 5), living in northern latitudes and insufficient intake of cholecalciferol and/or ergocalciferol.
• Vitamin D repletion and Vitamin D hormone replacement therapies of those patients in need thereof can provide blood concentrations of 25 -hydroxy vitamin D at or above 30 ng/mL and blood concentrations of 1,25- dihydroxyvitamin D within the patient's normal historical physiological range.
• One or both of the Vitamin D repletion and Vitamin D hormone replacement therapies, and preferably both, are preferably administered in a manner to avoid bolus surges of Vitamin D in the intestinal lumen or in the blood, thereby avoiding substantially increased risk of hypercalcemia, hyperphosphatemia or over suppression of plasma iPTH in the patient, all of which have been recognized as risks when treatment with a vitamin D therapy is undertaken.
• blood levels of 25 -hydroxy vitamin D are maintained above 30 ng/mL and blood levels of 1,25- dihydroxyvitamin D are maintained in the patient' s historical physiological range between therapeutic doses.
• the blood concentration of 25 -hydroxy vitamin D comprises predominantly 25 -hydroxy vitamin D 3 .
• the method includes administering predominantly or solely 25 -hydroxy vitamin D 3 for 25- hydroxy vitamin D repletion and/or maintenance. Atty. Docket No. 31138/43030A PATENT APPLICATION
• the invention provides a method of concurrently lowering or maintaining plasma iPTH levels, increasing or maintaining serum calcium levels, maintaining serum phosphorous levels, increasing or maintaining serum 25 -hydroxy vitamin D levels, and increasing or maintaining serum 1,25-dihydroxyvitamin D levels in a human patient by administering to the patient, as needed, effective amounts of both Vitamin D repletion and Vitamin D hormone replacement therapies.
• Many diseases manifest abnormal levels of more than one hormone and mineral.
• CKD for example, patients may experience decreases in serum total 1,25-dihydroxyvitamin D, increases in plasma iPTH, decreases in serum calcium and increases in serum phosphorous.
• Treatment in accordance with the present invention presents concurrent leveling and/or maintaining of these various hormone and mineral levels.
• the blood concentration of 25 -hydroxy vitamin D comprises predominantly 25 -hydroxy vitamin D 3 .
• the method includes administering predominantly or solely 25 -hydroxy vitamin D 3 for 25 -hydroxy vitamin D repletion and/or maintenance. Treatment of patients having Stage 3 or 4 CKD, or Stage 5 CKD, is particularly contemplated.
• the subject's PTH levels preferably are lowered by at least 30%, or alternatively to the target range for the CKD stage (e.g., for Stage 3 is 35-70 pg/mL (equivalent to 3.85-7.7 pmol/L), for Stage 4 is 70-110 pg/mL (equivalent to 7.7-12.1 pmol/L), and for Stage 5 is 150-300 pg/mL (equivalent to 16.5-33.0 pmol/L) (defined in K/DOQI Guideline No. I)).
• kits for treatment of a condition described herein such as Vitamin D deficiency or secondary hyperparathyroidism, including a 25 -hydroxy vitamin D compound, or an active Vitamin D hormone, or combinations thereof, and written instructions for co-treatment with a 25-hydroxyvitamin D compound and an active Vitamin D hormone.
• the kit can include a 25-hydroxyvitamin D compound, such as 25-hydroxyvitamin D 3 , and written instructions for co-treatment of a subject with the 25-hydroxyvitamin D compound and an active Vitamin D hormone, such as 1,25-dihydroxyvitamin D 2 .
• the kit can include an active Vitamin D hormone and written instructions for co-treatment of a subject with the active Vitamin D hormone and a 25-hydroxyvitamin D compound.
• the kit can include both a 25-hydroxyvitamin D compound and an active Vitamin D hormone, and written instructions for co-treatment of a subject with the 25- Atty. Docket No. 31138/43030A PATENT APPLICATION hydroxyvitamin D compound and the active Vitamin D hormone.
• Co-treatment can be according to the disclosure hereinbelow, and can include co-administration and administration at different discrete intervals but overlapping in a term of periodic administration of the compounds. Coadministration includes concurrent administration, and is not limited to simultaneous administration. Co-treatment can include administration by the same or different routes of administration.
• Co-administration means the administration of two or more compounds to the same patient.
• co-administration encompasses (a) simultaneous administration of a first and second compound and (b) administration of a first compound, followed by administration of a second compound.
• the first and second compounds can be administered within 24 hours, 8 hours, 4 hours, 2 hours, or 1 hour of each other. In other embodiments, different time periods of between administration of first and second compounds may be applicable.
• Vitamin D in reference to intraluminal, intracellular and blood levels of Vitamin D refers to a total concentration of the vitamin D compound markedly greater than the generally stable levels observed in a Vitamin D-replete subject, animal or human patient over the course of any 24-hour period by laboratory measurement when Vitamin D supplementation has been withheld for at least 30 days.
• “Adverse supraphysiologic surge” refers to a local or serum concentration of a vitamin D compound that elicits adverse effects such as excessive extrarenal hormone production, leading to local adverse effects on calcium and phosphorus metabolism, inhibition of hepatic 25-hydroxylation of vitamin D, increased catabolism of both Vitamin D and 25 -hydroxyvitamin D, hypercalciuria, hypercalcemia and/or hyperphosphatemia, with possible cardiovascular sequelae.
• the term "patient's normal historical physiological range of serum 1,25- dihydroxyvitamin D” refers to the average blood concentration range of 1,25-dihydroxyvitamin D of a patient based on at least two annual or biannual readings of serum 1,25-dihydroxyvitamin D levels taken while the kidneys are healthy.
• hypocalcemia refers to condition in a patient wherein the patient has corrected serum levels of calcium above 10.2 mg/dL. Normal corrected serum levels of calcium for a human are between about 8.6 to 10.2 mg/dL. Atty. Docket No. 31138/43030A PATENT APPLICATION
• hypoparathyroidism refers to primary hyperparathyroidism, secondary hyperparathyroidism and hyperparathyroidism secondary to chronic kidney disease (Stage 3, 4 or 5).
• subject generally includes humans, mammals (e.g., dogs, cats, rodents, sheep, horses, cows, goats), veterinary animals and zoo animals.
• hypophosphatemia refers to a condition in a patient having normal kidney function, or Stage 1-4 CKD, wherein the patient has serum phosphorous levels above 4.6 mg/dL. In a patient who has Stage 5 CKD, hyperphosphatemia occurs when the patient has serum levels above 5.5 mg/dL. Normal values for serum phosphorous in a human are 2.4-4.5 mg/dL.
• over suppression of plasma iPTH refers to a condition in a patient having normal kidney function, or Stage 1-3 CKD, wherein the patient has levels of plasma iPTH below 15 pg/mL.
• over suppression of plasma iPTH occurs when the patient has levels of plasma iPTH below 30 pg/mL.
• over suppression of plasma iPTH occurs when the patient has levels of plasma iPTH below 100 pg/mL.
• abnormally low bone turnover rate refers to a condition in a patient wherein the rate of bone resorption is greater than the rate of bone formation.
• Vitamin D repletion therapy refers to the administration to a patient of an effective amount of a Vitamin D, a Vitamin D analog, a Vitamin D prohormone, and a Vitamin D prohormone analog. Particularly preferred are ergocalciferol, cholecalciferol, 25 -hydroxy vitamin D 2 , and 25 -hydroxy vitamin D 3 .
• the Vitamin D repletion therapy can be via any route of administration. In one preferred embodiment, the therapy will result in blood concentration of 25-hydroxyvitamin D comprising predominantly 25-hydroxyvitamin D 3 .
• the blood concentration of 25-hydroxyvitamin D will comprise greater than 50% 25-hydroxyvitamin D 3 , or at least 60%, at least 70%, at least 80%, or at least 90% 25-hydroxyvitamin D 3 .
• the therapy includes administering predominantly or solely 25-hydroxyvitamin D 3 for 25-hydroxyvitamin D repletion and/or maintenance.
• the Atty. Docket No. 31138/43030A PATENT APPLICATION administration of 25-hydroxyvitamin D will comprise greater than 50% 25 -hydroxy vitamin D 3 , or at least 60%, at least 70%, at least 80%, at least 90%, or solely 25-hydroxyvitamin D 3 .
• Vitamin D hormone replacement therapy refers to the administration to a patient of an effective amount of one or more of active vitamin D hormones, which include an active Vitamin D hormone metabolites, and active Vitamin D hormone analogs, such as l ⁇ -hydroxylated Vitamin D compounds. Metabolites and analogs of Vitamin D which can substantially occupy the intracellular VDR or activate the VDR are preferred. 1,25- dihydroxyvitamin D 2 , 1,25-dihydroxyvitamin D 3 , 1,25-dihydroxyvitamin D 4 , and analogs thereof are preferred.
• controlled release and “sustained release” are used interchangeably, and refer to the release of the administered vitamin D compound in a way that deviates from immediate release.
• controlled release optionally includes delayed release characteristics.
• a delayed release type of controlled release formulation will be characterized by Cmax at a time greater than Cmax for an immediate release formulation.
• the release of an administered Vitamin D compound will preferably be at such a rate that total serum or blood levels of the Vitamin D compound are maintained or elevated above predosing levels for an extended period of time, e.g. 25-hydroxyvitamin D elevated for 4 to 24 hours or even longer.
• a sustained release type of controlled release formulation will be characterized by release at such a rate that total serum or blood levels of an active Vitamin D hormone are maintained or elevated above predosing levels for an extended period of time, e.g. 20 to 40 minutes, 1 to 15 hours or even longer.
• the release rate of the vitamin D compound is controlled to reduce Cmax and/or delay Tmax and/or decrease Cmax 24hr /C 24hr as described herein. Preferably both Cmax is reduced and Tmax is delayed (increased).
• one embodiment includes a method of administering an amount of a vitamin D compound to a subject such that the maximum serum concentration of the vitamin D compound in a dose interval (Cmax) is reduced as compared to Cmax for an equivalent amount of a vitamin Atty.
• Cmax maximum serum concentration of the vitamin D compound in a dose interval
• D compound administered by bolus IV injection and/or an equivalent immediate-release, oral dosage form is preferably by a factor of at least 50%, 60%, 70%, or 80%.
• Another embodiment of the includes a method of administering an amount of a vitamin D compound to a subject such that the maximum change in serum concentration of a vitamin D compound in a dose interval is reduced as compared to an equivalent amount of a vitamin D compound administered by bolus IV injection and/or an equivalent immediate-release, oral dosage form.
• the reduction is preferably by a factor of at least 50%, 60%, 70%, or 80%.
• Still another embodiment includes a method of administering an amount of a vitamin D compound to a patient such that the ratio of the maximum serum concentration within 24 hours after administration of a vitamin D compound to the concentration 24 hours after administration (Cmax 2 4hr/C24hr) is reduced as compared to an equivalent amount of a vitamin D compound administered by bolus IV injection and/or an equivalent immediate-release, oral dosage form.
• the reduction is preferably by a factor of at least 50%, 60%, 70%, or 80%.
• Yet another embodiment includes a method of administering an amount of a vitamin D compound to a subject such that the elimination half-life (t 1/2 ) of a vitamin D compound is increased as compared to t 1/2 for an equivalent amount of a vitamin D compound administered by bolus IV injection and/or an equivalent immediate-release, oral dosage form.
• the increase is preferably by a factor of at least 25%, 30%, 40%, 50%, or 60%.
• a further embodiment includes a method of administering an amount of a vitamin D compound to a subject such that the time for the plasma concentration of a vitamin D compound to reach its maximum in a dose interval following administration (Tmax) is increased as compared to Tmax for an equivalent amount of a vitamin D compound administered by bolus IV injection and/or an equivalent immediate-release, oral dosage form.
• Tmax dose interval following administration
• the increase is preferably by a factor of at least 25%, 30%, 40%, 50%, or 60%.
• compositions optionally can be designed for delayed release into the ileum of the gastrointestinal tract of humans or animals. It is contemplated that in one type of embodiment the compositions will ensure a substantially constant concentration of the desired Atty. Docket No. 31138/43030A PATENT APPLICATION
• Vitamin D compound in the body and a more sustained blood level.
• blood, intraluminal and intracellular concentration spikes e.g., adverse supraphysiologic levels, are mitigated or eliminated.
• Ergocalciferol, cholecalciferol, 25 -hydroxy vitamin D 2 and/or 25 -hydroxy vitamin D 2 1,25-dihydroxyvitamin D 3 , 1,25-dihydroxyvitamin D 2 , 1,25-dihydroxyvitamin D 4 , and other metabolites and analogs of Vitamin D are also useful as active compounds in pharmaceutical compositions.
• the pharmacologically active analogs of this invention can be processed in accordance with conventional methods of pharmacy to produce pharmaceutical agents for administration to patients, e.g., in admixtures with conventional excipients such as pharmaceutically acceptable organic or inorganic carrier substances suitable for parenteral, enteral (e.g., oral), topical or transdermal application which do not deleteriously react with the active compounds.
• Suitable pharmaceutically acceptable carriers include, but are not limited to, water, salt (buffer) solutions, alcohols, gum arabic, mineral and vegetable oils, benzyl alcohols, polyethylene glycols, gelatin, carbohydrates such as lactose, amylose or starch, magnesium stearate, talc, silicic acid, viscous paraffin, perfume oil, fatty acid monoglycerides and diglycerides, pentaerythritol fatty acid esters, hydroxy methylcellulose, polyvinyl pyrrolidone, etc.
• the pharmaceutical preparations can be sterilized and, if desired, mixed with auxiliary agents, e.g., lubricants, preservatives, stabilizers, wetting agents, emulsifiers, salts for influencing osmotic pressure, buffers, coloring, flavoring and/or aromatic active compounds.
• auxiliary agents e.g., lubricants, preservatives, stabilizers, wetting agents, emulsifiers, salts for influencing osmotic pressure, buffers, coloring, flavoring and/or aromatic active compounds.
• a pharmaceutically acceptable solid carrier is used, the dosage form of the analogs may be tablets, capsules, powders, suppositories, or lozenges.
• a liquid carrier soft gelatin capsules, transdermal patches, aerosol sprays, topical creams, syrups or liquid suspensions, emulsions or solutions may be the dosage form.
• injectable, sterile solutions preferably oily or aqueous solutions, as well as suspensions, emulsions, or implants, including suppositories.
• Ampoules are convenient unit dosages. Atty. Docket No. 31138/43030A PATENT APPLICATION
• Suitable enteral application particularly suitable are tablets, dragees, liquids, drops, suppositories, or capsules such as soft gelatin capsules.
• a syrup, elixir, or the like can be used wherein a sweetened vehicle is employed.
• Controlled release compositions can be formulated, e.g., liposomes or those wherein the active compound is protected with differentially degradable coatings, such as by microencapsulation, multiple coatings, etc. It is also possible to freeze-dry the new compounds and use the lypolizates obtained, for example, for the preparation of products for injection. Transdermal delivery of pharmaceutical compositions of the compounds of the invention is also possible.
• viscous to semisolid or solid forms comprising a carrier compatible with topical application and having a dynamic viscosity preferably greater than water.
• suitable formulations include, but are not limited to, solutions, suspensions, emulsions, creams, ointments, powders, liniments, salves, aerosols, etc., which are, if desired, sterilized or mixed with auxiliary agents, e.g., preservatives, etc.
• the dosage forms may also contain adjuvants, such as preserving or stabilizing adjuvants. They may also contain other therapeutically valuable substances or may contain more than one of the compounds specified herein and in the claims in admixture.
• Vitamin D repletion and Vitamin D hormone replacement therapies are preferably administered to the human patients in oral or intravenous dosage formulations.
• the administration of such therapies can be on an episodic basis, suitably from daily, to 1 to 3 times a week.
• the dosage of Vitamin D repletion therapy or Vitamin D hormone replacement therapy is about 0.5 ⁇ g to about 400 ⁇ g per week, depending on the agent selected.
• such therapies can be given in a unit dosage form between about 0.5 ⁇ g to about 100 ⁇ g, or about 0.5 ⁇ g to about 10 ⁇ g in a Atty. Docket No. 31138/43030A PATENT APPLICATION pharmaceutically acceptable carrier per unit dosage.
• Episodic doses can be a single dose or, optionally, divided into 2-4 subdoses which, if desired, can be given, e.g., twenty minutes to an hour apart until the total dose is given.
• the dosage of a 1,25-dihydroxyvitamin D for oral administration generally is about 0.1 ⁇ g per week to 100 ⁇ g per week, preferably about 0.7 ⁇ g per week to about 70 ⁇ g per week, which can be split into daily or other periodic doses, such as three times per week for administration concomitant with hemodialysis.
• an oral dosage equivalent to about 1, 2, 3, 4, 5, 6, 7, 8 or 9 ⁇ g per day is contemplated.
• a 1,25-dihydroxyvitamin D compound can be dispensed by unit dosage form comprising about 0.1 ⁇ g to about 10 ⁇ g per unit dosage, for example about 1 ⁇ g to about 4 ⁇ g, about 2 ⁇ g to about 10 ⁇ g, or about 3 ⁇ g to about 5 ⁇ g.
• the duration of the treatment is contemplated to be at least four weeks, or at least twelve weeks, and can be ongoing for years or even decades.
• a controlled release composition intended for oral administration for Vitamin D repletion in accordance with the methods described herein preferably is designed to contain concentrations of the 25 -hydroxy vitamin D 3 , for example, of 1 to 100 ⁇ g per unit dose and are prepared in such a manner as to effect controlled or substantially constant release of the 25- hydroxyvitamin D, optionally into the ileum of the gastrointestinal tract, of humans or animals over an extended period of time.
• the compositions and methods may provide substantially increased absorption of 25 -hydroxy vitamin D via transport on DBP and decreased absorption via transport in chylomicrons.
• the compositions and methods may provide maintenance of substantially constant blood levels of 25 -hydroxy vitamin D during the 24-hour post-dosing period.
• the compound, such as 25 -hydroxy vitamin D 3 , together with other therapeutic agents can be orally or intravenously administered in accordance with the above described embodiments in dosage amounts of from 1 to 100 ⁇ g per day, with the preferred Atty. Docket No. 31138/43030A PATENT APPLICATION dosage amounts of from 5 to 50 ⁇ g per day, for example about 10 to 25 ⁇ g. Preferred doses will provide an average rise in serum 25 -hydroxy vitamin D 3 of about 1 to 3 ng/mL.
• the method is contemplated to include administering a formulation described herein to raise and preferably also maintain blood 1,25-dihydroxyvitamin D levels at 25 pg/mL, 30 pg/mL, or higher, e.g. 25-65 pg/mL for an extended period, for example at least one month, at least three months, at least six months, or longer.
• Dosages for a given patient can be determined using conventional considerations, e.g., by customary comparison of the differential activities of the subject compounds and of a known agent, such as by means of an appropriate conventional pharmacological protocol.
• a physician of ordinary skill can readily determine and prescribe the effective amount of the drug required to counter or arrest the progress of the condition.
• Optimal precision in achieving concentrations of drug within the range that yields efficacy without toxicity requires a regimen based on the kinetics of the drug's availability to target sites. This involves a consideration of the distribution, equilibrium, and elimination of a drug.
• the dosage of active ingredient in the compositions of this invention may be varied; however, it is necessary that the amount of the active ingredient be such that an efficacious dosage is obtained.
• the active ingredient is administered to patients (animal and human) in need of treatment in dosages that will provide optimal pharmaceutical efficacy.
• Vitamin D repletion and Vitamin D hormone replacement therapies has improved efficacy in reducing or preventing elevated blood PTH levels as well as maintaining adequate and appropriate levels of serum calcium, serum phosphorous, serum total 25 -hydroxy vitamin D and serum total 1,25-dihydroxyvitamin D.
• Example 1 Efficacy Study in Adult Patients With CKD and Secondary Hyperparathyroidism
• Vitamin D The effectiveness of three different Vitamin D treatment regimens in controlling elevated serum iPTH is examined in a 26-week study of non-obese patients diagnosed with secondary hyperparathyroidism and CKD.
• Two formulations containing Vitamin D are prepared.
• One of the formulations (Formulation #1) is a soft gelatin capsule containing 5,000 IU of Vitamin D, comprised of a mixture of 2,500 IU of cholecalciferol and 2,500 IU of ergocalciferol and prepared in a delayed sustained release formulation.
• the second formulation (Formulation #2) is soft gelatin capsule of identical appearance containing 0.5 meg of 1,25- dihydroxyvitamin D 2 prepared in a delayed sustained release formulation.
• a fasting morning blood sample is drawn from each subject, irrespective of treatment group, at weekly intervals just prior to dosing.
• All collected blood is analyzed for the contained levels of 25- hydroxyvitamin D, 1,25-dihydroxyvitamin D, plasma iPTH, serum calcium and serum phosphorus, and the data are analyzed by treatment group.
• Subjects in all four treatment groups exhibit mean baseline serum total 25 -hydroxy vitamin D levels of approximately 8-11 ng/mL, based on analysis of fasting blood samples drawn on Days 1 through 3.
• Subjects in Group #4 show no significant changes in any of the parameters measured over the course of the study.
• Subjects in Group #1 show during treatment a steadily increasing mean serum 25- hydroxyvitamin D reaching approximately 34 ng/mL, a significant reduction in plasma iPTH, and no significant changes in the other measured parameters.
• Subjects in Group #2 show a significant increase in serum total 1,25-dihydroxyvitamin D, a significant decrease in iPTH, slightly increasing trends in serum calcium and serum phosphorus, and no significant changes in mean serum 25 -hydroxy vitamin D.
• Subjects in Group #3 exhibit the same changes observed in Group #2 except that (a) the decrease in iPTH over the course of the treatment period is significantly greater by study end than in Groups #1 and #2, and (b) serum total 25- hydroxyvitamin D show steadily increasing mean serum 25 -hydroxy vitamin D reaching approximately 36 ng/mL by Week 26.
• Example 2 Efficacy Study in Adult Patients With CKD and Secondary Hyperparathyroidism
• Vitamin D The effectiveness of three different Vitamin D treatment regimens in controlling elevated serum iPTH is examined in a 26-week study of non-obese patients diagnosed with Atty. Docket No. 31138/43030A PATENT APPLICATION secondary hyperparathyroidism and CKD.
• Two formulations containing Vitamin D are prepared.
• One of the formulations (Formulation #1) is a soft gelatin capsule containing 5,000 IU of Vitamin D, comprised of a mixture of 4,000 IU of cholecalciferol and 1,000 IU of ergocalciferol and prepared in a delayed sustained release formulation.
• the second formulation (Formulation #2) is soft gelatin capsule of identical appearance containing 0.5 meg of 1,25- dihydroxyvitamin D 2 prepared in a delayed sustained release formulation.
• a fasting morning blood sample is drawn from each subject, irrespective of treatment group, at weekly intervals just prior to dosing.
• All collected blood is analyzed for the contained levels of 25- hydroxyvitamin D, 1,25-dihydroxyvitamin D, plasma iPTH, serum calcium and serum phosphorus, and the data are analyzed by treatment group.
• Subjects in all four treatment groups exhibit mean baseline serum total 25 -hydroxy vitamin D levels of approximately 8-11 ng/mL, based on analysis of fasting blood samples drawn on Days 1 through 3.
• Subjects in Group #4 show no significant changes in any of the parameters measured over the course of the study.
• Subjects in Group #1 show during treatment a significant increase in mean serum 25 -hydroxy vitamin D (with the predominant species being 25 -hydroxy vitamin D 3 ), a significant reduction in plasma iPTH, and no significant changes in the other measured parameters.
• Subjects in Group #2 show a significant increase in serum total 1,25-dihydroxyvitamin D, a significant decrease in iPTH, slightly increasing trends in serum calcium and serum phosphorus, and no significant changes in mean serum 25 -hydroxy vitamin D.
• Subjects in Group #3 exhibit the same changes observed in Group #2 except that (a) the decrease in iPTH over the course of the treatment period is significantly greater by study end than in Groups #1 and #2, and (b) serum total 25 -hydroxy vitamin D show significantly increased mean serum 25 -hydroxy vitamin D by Week 26.

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