WO1998057656A1 - A combined pharmaceutical preparation comprising parathyroid hormone and a bone resorption inhibitor - Google Patents
A combined pharmaceutical preparation comprising parathyroid hormone and a bone resorption inhibitor Download PDFInfo
- Publication number
- WO1998057656A1 WO1998057656A1 PCT/SE1998/001095 SE9801095W WO9857656A1 WO 1998057656 A1 WO1998057656 A1 WO 1998057656A1 SE 9801095 W SE9801095 W SE 9801095W WO 9857656 A1 WO9857656 A1 WO 9857656A1
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- Prior art keywords
- bone
- parathyroid hormone
- months
- administration
- inhibitor
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Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/22—Hormones
- A61K38/29—Parathyroid hormone (parathormone); Parathyroid hormone-related peptides
-
- 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
- A61K31/13—Amines
- A61K31/135—Amines having aromatic rings, e.g. ketamine, nortriptyline
- A61K31/138—Aryloxyalkylamines, e.g. propranolol, tamoxifen, phenoxybenzamine
-
- 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
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/452—Piperidinium derivatives
-
- 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
- A61K31/56—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
-
- 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
- A61K31/66—Phosphorus compounds
-
- 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
- A61K31/66—Phosphorus compounds
- A61K31/662—Phosphorus acids or esters thereof having P—C bonds, e.g. foscarnet, trichlorfon
- A61K31/663—Compounds having two or more phosphorus acid groups or esters thereof, e.g. clodronic acid, pamidronic acid
-
- 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
- A61K31/66—Phosphorus compounds
- A61K31/675—Phosphorus compounds having nitrogen as a ring hetero atom, e.g. pyridoxal phosphate
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
- A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/12—Drugs for disorders of the metabolism for electrolyte homeostasis
- A61P3/14—Drugs for disorders of the metabolism for electrolyte homeostasis for calcium homeostasis
-
- 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
- bone is continuously subject to remodeling.
- This is a process where bone resorption is closely linked to bone formation, through the concerted action of the bone active cells, i.e. the bone forming osteoblasts and the bone resorbing osteoclasts. These cells together form what is called a basal multicellular (metabolic) unit, or BMU.
- the remodeling process starts with activation of the lining cells (the cells that cover the unmineralized bone).
- the lining cells resorb the unmineralized bone, then retract and leave room for the osteoclasts which resorb the old, mineralized bone and create an environment which attracts the osteoblast to the same site.
- the osteoblasts thereafter lay down the organic matrix, which subsequently is becoming mineralized to form new bone.
- the resulting bone mass is thus determined by the balance between resorption by osteoclasts and formation by osteoblasts.
- the coupling phenomenon means that even when the intention is to produce a positive balance per cycle it is still necessary to start with bone resorption.
- a BMU cycle takes 3 to 6 months to complete.
- the rate by which the basal metabolic (multicellular) units are being activated, the activation frequency also plays a role.
- a high activation frequency increases the rate by which bone is being lost if there is a negative balance per remodeling cycle.
- activation frequency is increased the space that is being occupied by remodeling, the remodeling space, is also increased. This will give a lowered bone mass, since a greater portion of the bone is subject to resorption as part of the remodeling process.
- Osteoporosis is a disease which is characterized by a reduced amount of bone tissue, usually of normal composition, which has reduced strength due to a combination of low bone mass and impaired architecture, and therefore carries an increased risk of fractures.
- osteoporosis is the result of negative bone balance per remodeling cycle, i.e. less bone is formed than is being resorbed.
- a specific disease as responsible for the loss of bone (e.g. malabsorption of calcium and hypersecretion of corticosteroid hormones) but in the majority of patients no such disorder is identified.
- Such patients are classified as having "primary" osteoporosis. Bone is lost with advancing age in both sexes, but in females there is generally an increased rate of loss during the first years after the menopause (hence the term "postmenopausal" osteoporosis).
- a number of agents have been used for the prevention and treatment of bone loss and osteoporosis, e.g. estrogen, vitamin D and bisphosphonates, such as alendronate (for a review, see: Osteoporosis (Marcus, R., Feldman, D. and Kelsey, F., Eds.) Academic Press, San Diego, 1996).
- Such agents mainly act through inhibition of bone resorption.
- the antireso ⁇ tive agents can retard bone loss but, by definition, they do not increase bone mass within each remodeling unit. Many patients with fractures have severe bone loss at the time they come to clinical attention. Inhibition of bone resorption might not be enough to prevent fracture recurrences. Therefore it is urgent to develop therapies that can increase bone mass, i.e. anabolic agents.
- Parathyroid hormone is an 84 amino acid polypeptide which is normally secreted from the parathyroid glands. PTH has an important physiological role to maintain serum calcium within a narrow range. Furthermore, it has anabolic properties when given intermittently. This has been well documented in a number of animal and open clinical studies, recently reviewed by Dempster, D.W. et al. (Endocrine Reviews 1993, vol. 14, 690-709). PTH has a multitude of effects on bone. Part of it is through the remodeling cycle. PTH causes both increased activation frequency and a positive balance per cycle.
- Human PTH may be obtained through peptide synthesis or from genetically engineered yeast, bacterial or mammalian cell hosts. Synthetic human PTH is commercially available from Bachem Inc., Bubendorf, Switzerland. Production of recombinant human parathyroid hormone is disclosed in e.g. EP-B-0383751. PTH when given alone, to a patient with osteoporosis, will stimulate bone formation within each remodeling cycle and cause a positive bone balance within each cycle. At the same time the number of remodeling units will greatly increase, i.e. the activation frequency is enhanced. These two mechanisms act in different directions on bone mass.
- the activation frequency is doubled.
- bone mass or bone density
- bone mineral density is increased by 5 to 10% per year in the lumbar spine and is largely unaffected in the femoral neck, which contains a higher proportion of cortical bone.
- the presently known methods for treatment of osteoporosis utilize bone reso ⁇ tion inhibition of the BMU cycle, but have the drawbacks that their onset of effect is slow and limited, and that they only cause moderate increases of bone mineral density (bone mass) and may therefore be insufficient for the treatment of patients with osteoporosis in a stage where there is high risk of recurrent fractures. Furthermore, it has not been shown that present methods can improve on the altered architecture that is a hallmark of advanced osteoporosis.
- a method of treatment of bone metabolism disorders utilizing the order of events in the BMU cycle, and comprising administering a bone active phosphonate and, sequentially, parathyroid hormone, is disclosed in WO 96/07417 (The Procter & Gamble Company).
- the bone active phosphonate is given for a period of greater than about 6 months, in various dosage regimens, but always prior to PTH.
- Hodsman, A. et al. J. Bone and Mineral Research, Vol. 10, Suppl. 1, abstract No. P288, p. S200, 1995 discloses a clinical trial involving treatment with PTH for 28 days, with our without sequential calcitonin for 42 days, with this cycle repeated at 3 months intervals for 2 years. Patients were then crossed over to clodronate, 28 days per 3 months, for one year. However, there was no beneficial effect in bone density from this sequential PTH/bisphosphonate treatment regimen.
- WO 97/31640 discloses a pharmaceutical composition comprising (a) an estrogen agonist antagonist; and (b) a bone activating compound, such as parathyroid hormone.
- a pharmaceutical composition comprising (a) an estrogen agonist antagonist; and (b) a bone activating compound, such as parathyroid hormone.
- the periods of treatment are broadly defined and it is stated that the said compounds can be administered for periods from about three months to about three years.
- the present invention is thus based on the concept of remodeling.
- overriding the reso ⁇ tive phase of the BMU over several consecutive cycles it fortifies the anabolic action of PTH.
- prolonging the treatment over several BMU cycles it takes advantage of the opposite influences on the activation frequency which is increased by PTH and later reduced by bisphosphonates.
- WO 96/07417 discloses a method of treatment of bone metabolism disorders, comprising administering a bone active phosphonate and, subsequently, parathyroid hormone.
- the bone active phosphonate was thus given prior to PTH.
- the order of treatment regimens provides principally different treatment responses. Slowing down the remodeling cycle with a reso ⁇ tion inhibitor would limit the maximum anabolic effect that can be obtained with PTH.
- PTH is given first over several BMU cycles, not only will it enhance the BMU positive bone balance significantly, it will also increase activation frequency to such an extent that effects of subsequent antireso ⁇ tive therapy will be enhanced.
- a bisphosphonate is given after PTH treatment, in order not only to maintain bone mass on the higher level by its antireso ⁇ tive action, but also to increase BMD by filling in the increased remodeling space through the reduction of activation frequency.
- treatment with an agent that increases the activation frequency must be of sufficient duration, i.e. it must cover several BMU cycles (e.g. 6 to 12 months). Only then can the full potential of the treatment, with regards to increases in BMD, develop. It has thus su ⁇ risingly been found that the method of treatment according to the invention achieves the advantageous result that bone mass is first rapidly increased during PTH treatment and thereafter further bone mineral density is gained, compared to the results achieved with bisphosphonates alone without prior activation by PTH.
- the present invention provides in a first aspect a combined pharmaceutical preparation comprising parathyroid hormone and a bone reso ⁇ tion inhibitor, said preparation being adapted for (a) the administration of parathyroid hormone during a period of approximately 6 to 24 months, preferably about 12 (or above 12) months to 24 months or about 12 (or above 12) months to 18 months, or more preferably about 18 months; and (b) after the administration of said parathyroid hormone has been terminated, the administration of a bone reso ⁇ tion inhibitor during a period of approximately 6 to 36 months, preferably about 12 to 36 months or about 12 to 18 months, or more preferably about 12 months.
- This sequence of treatments can be repeated at intervals of one to five years, until BMD has reached a value corresponding to "young normal mean".
- the interval between treatments coincides with the period of one treatment cycle, i.e. 12 to 60 months, preferably 24 to 60 months or 24 to 42 months, or more preferably 30 to 36 months.
- PTH parathyroid hormone
- thyroid hormone encompasses full-length PTH(l-84) as well as PTH fragments. It will thus be understood that fragments of PTH variants, in amounts giving equivalent biological activity to PTH(l-84), can be inco ⁇ orated in the formulations according to the invention, if desired. Fragments of PTH inco ⁇ orate at least the amino acid residues of PTH necessary for a biological activity similar to that of intact PTH. Examples of such fragments are PTH(1-31), PTH(l-34), PTH(l-36), PTH(l-37), PTH(l-38), PTH(1- 41), PTH(28-48) and PTH(25-39).
- thyroid hormone also encompasses variants and functional analogues of PTH.
- the present invention thus includes pharmaceutical formulations comprising such PTH variants and functional analogues, carrying modifications like substitutions, deletions, insertions, inversions or cyclisations, but nevertheless having substantially the biological activities of parathyroid hormone.
- Stability-enhanced variants of PTH are known in the art from e.g. WO 92/11286 and WO 93/20203.
- Variants of PTH can e.g. inco ⁇ orate amino acid substitutions that improve PTH stability and half-life, such as the replacement of methionine residues at positions 8 and/or 18, and replacement of asparagine at position 16.
- Cyclized PTH analogues are disclosed in e.g. WO 98/05683.
- the invention includes a preparation as described above wherein the said parathyroid hormone is selected from the group consisting of: (a) full-length parathyroid hormone; (b) biologically active variants of full-length parathyroid hormone;
- biologically active should be understood as eliciting a sufficient response in a bioassay for PTH activity, such as the rat osteosarcoma cell-based assay for PTH-stimulated adenylate cyclase production (see Rodan et al. (1983) J. Clin. Invest. 72, 1511; and Rabbani et al. (1988) Endocrinol. 123, 2709).
- the PTH to be used in the pharmaceutical preparation according to the invention is preferably recombinant human PTH, such as full-length recombinant human PTH.
- Parathyroid hormone can be subcutaneously administered in an amount of approximately 0.1 to 5 ⁇ g/kg body weight, preferably 0.5 to 3 ⁇ g/kg, or more preferably 1 to 2.5 ⁇ g/kg body weight.
- nasally or pulmonary, PTH can be administered in an amount of 0.1 ⁇ g to 15 mg/kg.
- the said bone reso ⁇ tion inhibitor can be a bisphosphonate, e.g. alendronate; or a substance with estrogen-like effect, e.g. estrogen; or a selective estrogen receptor modulator, e.g. raloxifene, tamoxifene, droloxifene, toremifene, idoxifene, or levormeloxifene; or a calcitonin-like substance, e.g. calcitonin; or a vitamin D analog; or a calcium salt.
- a bisphosphonate e.g. alendronate
- a substance with estrogen-like effect e.g. estrogen
- a selective estrogen receptor modulator e.g. raloxifene, tamoxifene, droloxifene, toremifene, idoxifene, or levormeloxifene
- a calcitonin-like substance e.g. calcit
- the said bone reso ⁇ tion inhibitor is preferably administered in an amount of 0.05 to 500 mg, preferably around 10 mg.
- the invention provides the use of parathyroid hormone in combination with a bone reso ⁇ tion inhibitor in the manufacture of a medicament for the treatment or prevention of bone-related diseases, in particular osteoporosis, said medicament being adapted for (a) the administration of parathyroid hormone during a period of approximately 6 to 24 months; (b) after the administration of parathyroid hormone has been terminated, the administration of a bone reso ⁇ tion inhibitor during a period of approximately 12 to 36 months.
- the parathyroid hormone and the bone reso ⁇ tion inhibitor are as defined above.
- the invention provides a method of treatment or prevention of bone- related diseases, in particular osteoporosis, which comprises administering to a mammal, including man, in need of such treatment an effective amount of a pharmaceutical preparation as defined in the above. Consequently, such a method comprises administering to a mammal, including man, in need of such treatment (a) an effective amount of parathyroid hormone during a period of approximately 6 to 24 months; and (b) after the administration of parathyroid hormone has been terminated, an effective amount of a bone reso ⁇ tion inhibitor during a period of approximately 12 to 36 months.
- the invention also includes a method of treatment or prevention of bone-related diseases which comprises administering, to a patient who has already been subject to treatment with parathyroid hormone during a period of approximately 6 to 24 months, after the administration of parathyroid hormone has been terminated, an effective amount of a bone reso ⁇ tion inhibitor during a period of approximately 12 to 36 months.
Abstract
Description
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Priority Applications (15)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP98929965A EP1001802B1 (en) | 1997-06-19 | 1998-06-08 | A combined pharmaceutical preparation comprising parathyroid hormone and a bone resorption inhibitor |
DE69826132T DE69826132T2 (en) | 1997-06-19 | 1998-06-08 | PHARMACEUTICAL COMBINATION PREPARATION FROM PARATHORMONE AND AN INHIBITOR OF BONE RESORPTION |
AT98929965T ATE275419T1 (en) | 1997-06-19 | 1998-06-08 | PHARMACEUTICAL COMBINATION PREPARATION OF PARATHORMONE AND A BONE RESORPTION INHIBITOR |
AU79458/98A AU753477B2 (en) | 1997-06-19 | 1998-06-08 | A combined pharmaceutical preparation comprising parathyroid hormone and a bone resorption inhibitor |
JP50425999A JP4989811B2 (en) | 1997-06-19 | 1998-06-08 | Combined pharmaceutical preparation containing parathyroid hormone and bone resorption inhibitor |
US09/125,247 US6284730B1 (en) | 1997-06-19 | 1998-06-08 | Methods useful in the treatment of bone resorption diseases |
DK98929965T DK1001802T3 (en) | 1997-06-19 | 1998-06-08 | Pharmaceutical combination drug of parathyroid hormone and a bone resorption inhibitor |
CA2294101A CA2294101C (en) | 1997-06-19 | 1998-06-08 | A combined pharmaceutical preparation comprising parathyroid hormone and a bone resorption inhibitor |
HK00107524A HK1029738A1 (en) | 1997-06-19 | 2000-11-23 | A combined pharmaceutical preparation comprising parathyroid hormone and a bone resorption inhibitor. |
US10/389,797 US7018982B2 (en) | 1997-06-19 | 2003-03-18 | Methods useful in the treatment of bone resorption diseases |
US11/305,339 US7507715B2 (en) | 1997-06-19 | 2005-12-19 | Methods useful in the treatment of bone resorption diseases |
US12/351,558 US7749543B2 (en) | 1997-06-19 | 2009-01-09 | Methods useful in the treatment of bone resorption diseases |
US12/822,089 US8153588B2 (en) | 1997-06-19 | 2010-06-23 | Methods useful in the treatment of bone resorption diseases |
US13/405,093 US8765674B2 (en) | 1997-06-19 | 2012-02-24 | Methods useful in the treatment of bone resorption diseases |
US14/285,437 US20140256632A1 (en) | 1997-06-19 | 2014-05-22 | Methods useful in the treatment of bone resorption diseases |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SE9702401A SE9702401D0 (en) | 1997-06-19 | 1997-06-19 | Pharmaceutical use |
SE9702401-2 | 1997-06-19 |
Related Child Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US09/125,247 A-371-Of-International US6284730B1 (en) | 1997-06-19 | 1998-06-08 | Methods useful in the treatment of bone resorption diseases |
US09/942,661 Continuation US20020002135A1 (en) | 1997-06-19 | 2001-08-31 | Pharmaceutical use |
Publications (1)
Publication Number | Publication Date |
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WO1998057656A1 true WO1998057656A1 (en) | 1998-12-23 |
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ID=20407482
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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PCT/SE1998/001095 WO1998057656A1 (en) | 1997-06-19 | 1998-06-08 | A combined pharmaceutical preparation comprising parathyroid hormone and a bone resorption inhibitor |
Country Status (15)
Country | Link |
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US (8) | US6284730B1 (en) |
EP (2) | EP1001802B1 (en) |
JP (3) | JP4989811B2 (en) |
AT (2) | ATE275419T1 (en) |
AU (1) | AU753477B2 (en) |
CA (2) | CA2294101C (en) |
CY (1) | CY1110287T1 (en) |
DE (2) | DE69841279D1 (en) |
DK (2) | DK1001802T3 (en) |
ES (2) | ES2229511T3 (en) |
HK (2) | HK1029738A1 (en) |
PT (2) | PT1001802E (en) |
SE (1) | SE9702401D0 (en) |
WO (1) | WO1998057656A1 (en) |
ZA (1) | ZA984947B (en) |
Cited By (6)
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WO2010115932A1 (en) * | 2009-04-08 | 2010-10-14 | Novartis Ag | Combination for the treatment of bone loss |
US8052987B2 (en) | 2000-06-20 | 2011-11-08 | Novartis Pharmaceuticals Corporation | Method of administering bisphosphonates |
US8153587B2 (en) | 2001-06-01 | 2012-04-10 | Novartis Ag | Orally administering parathyroid hormone and calcitonin |
WO2013088440A1 (en) | 2011-12-13 | 2013-06-20 | Amorphical Ltd. | Amorphous calcium carbonate for the treatment of calcium malabsorption and metabolic bone disorders |
US11052108B2 (en) | 2016-10-25 | 2021-07-06 | Amorphical Ltd. | Amorphous calcium carbonate for treating a leukemia |
US11052107B2 (en) | 2015-06-04 | 2021-07-06 | Amorphical Ltd. | Amorphous calcium carbonate stabilized with polyphosphates or bisphosphonates |
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SE9702401D0 (en) | 1997-06-19 | 1997-06-19 | Astra Ab | Pharmaceutical use |
CA2347330C (en) * | 2001-05-10 | 2002-03-12 | Pharmaceutical Partners Of Canada Inc. | Liquid injectable formulation of disodium pamidronate |
CA2451953A1 (en) * | 2001-06-28 | 2003-04-24 | Microchips, Inc. | Methods for hermetically sealing microchip reservoir devices |
TWI329105B (en) | 2002-02-01 | 2010-08-21 | Rigel Pharmaceuticals Inc | 2,4-pyrimidinediamine compounds and their uses |
WO2004022033A1 (en) * | 2002-09-04 | 2004-03-18 | Microchips, Inc. | Method and device for the controlled delivery of parathyroid hormone |
CN102358738A (en) | 2003-07-30 | 2012-02-22 | 里格尔药品股份有限公司 | 2,4-pyrimidinediamine compounds and uses of treating or preventing autoimmune diseases thereof |
US20050119183A1 (en) * | 2003-11-12 | 2005-06-02 | Nps Allelix Corp. | Method for treating bone loss using parathyroid hormone |
US7488316B2 (en) | 2005-01-25 | 2009-02-10 | Microchips, Inc. | Control of drug release by transient modification of local microenvironments |
WO2006135915A2 (en) | 2005-06-13 | 2006-12-21 | Rigel Pharmaceuticals, Inc. | Methods and compositions for treating degenerative bone disorders |
ES2279500T3 (en) * | 2005-06-17 | 2007-08-16 | Magneti Marelli Powertrain S.P.A. | FUEL INJECTOR. |
CN101355959B (en) * | 2005-11-10 | 2013-02-27 | 密歇根理工大学管理委员会 | Black bear parathyroid hormone and methods of using black bear parathyroid hormone |
CN102470164B (en) * | 2009-09-09 | 2014-04-09 | 旭化成制药株式会社 | PTH-containing therapeutic/prophylactic agent for osteoporosis, characterized in that PTH is administered once week at unit dose of 100 to 200 units |
JP2013512688A (en) | 2009-12-07 | 2013-04-18 | ミシガン テクノロジカル ユニバーシティ | Methods of using black bear parathyroid hormone and black bear parathyroid hormone |
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CN109568338A (en) * | 2011-12-13 | 2019-04-05 | 艾玛菲克有限公司 | For treating the bad amorphous calcium carbonate with bone metabolism disturbance of calcium uptake |
US10688124B2 (en) | 2011-12-13 | 2020-06-23 | Amorphical Ltd | Amorphous calcium carbonate for the treatment of calcium malabsorption and metabolic bone disorders |
US11052107B2 (en) | 2015-06-04 | 2021-07-06 | Amorphical Ltd. | Amorphous calcium carbonate stabilized with polyphosphates or bisphosphonates |
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