WO1994021266A1 - The use of bisphosphonates in bone surgery - Google Patents
The use of bisphosphonates in bone surgery Download PDFInfo
- Publication number
- WO1994021266A1 WO1994021266A1 PCT/FI1994/000091 FI9400091W WO9421266A1 WO 1994021266 A1 WO1994021266 A1 WO 1994021266A1 FI 9400091 W FI9400091 W FI 9400091W WO 9421266 A1 WO9421266 A1 WO 9421266A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- bone
- compound
- clodronate
- pharmaceutically acceptable
- surgery
- Prior art date
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L27/00—Materials for grafts or prostheses or for coating grafts or prostheses
- A61L27/50—Materials characterised by their function or physical properties, e.g. injectable or lubricating compositions, shape-memory materials, surface modified materials
- A61L27/54—Biologically active materials, e.g. therapeutic substances
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/02—Prostheses implantable into the body
- A61F2/28—Bones
-
- 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
- A61K31/675—Phosphorus compounds having nitrogen as a ring hetero atom, e.g. pyridoxal phosphate
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L27/00—Materials for grafts or prostheses or for coating grafts or prostheses
- A61L27/36—Materials for grafts or prostheses or for coating grafts or prostheses containing ingredients of undetermined constitution or reaction products thereof, e.g. transplant tissue, natural bone, extracellular matrix
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2300/00—Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices
- A61L2300/10—Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices containing or releasing inorganic materials
- A61L2300/112—Phosphorus-containing compounds, e.g. phosphates, phosphonates
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2300/00—Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices
- A61L2300/40—Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices characterised by a specific therapeutic activity or mode of action
- A61L2300/412—Tissue-regenerating or healing or proliferative agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2430/00—Materials or treatment for tissue regeneration
- A61L2430/02—Materials or treatment for tissue regeneration for reconstruction of bones; weight-bearing implants
Definitions
- This invention relates to the use of a certain group of bisphosphonates for the regeneration of bone tissue and/or elimination of late complications subsequent to bone surgery. More particularly, the invention concerns the use of clodronate to enhance bone tissue formation after surgical replacement of endo-osteal material such as implantations, particularly dental implantations, and transplantations.
- Bisphosphonates are synthetic organic compounds structurally related to pyrophosphate in that the pyrophosphate P-0-P-bond is replaced by a P-C-P-bond.
- bisphosphonates are resistent to enzymatic hydrolysis in osseous tissue.
- the bisphosphonates are potent inhibitors of bone resorption and they have been successfully used in the treatment of hypercalcemia caused by various reasons. A great number of bisphosphonates have been studied, but only clodronate, etidronate and pamidronate have reached wider clinical use.
- the main effect of the bisphosphonates is their ability to inhibit bone resorption, but contrary to the effect on mineralization, the mechanism involved is cellular (Fleisch H, Drugs 1991; 42: 919-44). These different effects vary greatly according to the structure of the individual bisphosphonate compound.
- the half-life of circulating bisphosphonates is very short, in the order of minutes to hours. Of a given dose, 20 to 50 % is taken up by the skeleton, the rest being excreted in the urine. The half- life in bone is far longer and depends upon the turnover rate of the skeleton itself.
- clodronate has been widely used in hypercalcemia and osteolysis of malignancy (Bonjour J P and Rizzoli R, Calcif Tissue Int 1990; 46 Suppl: 20-25). All published reports indicate that clodronate can normalize plasma calcium in the majority of hypercalcemic, rehydrated cancer patients in whom increased bone resporption is the prevailing disturbed calcium flux (Fleisch H, Drugs 1991; 42: 919-44).
- bisphosphonates are well documented with respect to their ability to inhibit bone resorption in connection with various diseases.
- the use of these compounds to promote bone tissue formation subsequent to surgical operations relating to endo-osteal prosthesis such as hip prostheses, plates used in internal rigid fixation and various kinds of implantations; osteomyelitis after decorticalization of necrotics from the mandible or bone transplantations has, however, never been suggested.
- the term "bone surgery” shall be understood to include surgical operations relating to endo-osteal prostheses such as hip prostheses, plates used in internal rigid fixation and various kinds of implantations of artificial implants into the human body such as dental implants; treatment of osteomyelitis after decorticalization of necrotics from the mandible; and bone transplantations.
- the invention particularly concerns oral surgery, especially the introduction of artificial tooth implants.
- the present invention relates to the use of a compound of formula (I)
- X is H, OH, Cl, F or a methyl group and Y is Cl, OH, -(CH 2 ) 2 -N(CH 3 )-(CH 2 ) 4 -CH 3 , -(CH 2 ) n -CH 3 or -(CH 2 ) n -NH 2 , where n is zero or an integer of 1 to 8, -NHZ, where Z is pyridinyl or cycloheptyl, -SZ', where Z' is pyridinyl or chloro-substituted phenyl, or Y is a pyridinylsubstituted lower alkyl chain; or a non-toxic, pharmaceutically acceptable salt or ester thereof for the manufacture of a pharmaceutical composition to be used in enhancing the formation of bone tissue and/or eliminating late complications subsequent to bone surgery in a bone surgery patient before and/or after said surgery.
- the present invention relates further to a method of enhancing the formation of bone tissue and/or eliminating late complications subsequent to bone surgery comprising administering an amount, which is safe and sufficient to promote the formation of bone tissue and/or eliminate late complications, of a compound of formula (I)
- n is zero or an integer of 1 to 8
- -NHZ where Z is pyridinyl or cycloheptyl
- -SZ' where Z' is pyridinyl or chloro-substituted phenyl
- Y is a pyridinylsubstituted lower alkyl chain; or a non-toxic, pharmaceutically acceptable salt or ester thereof to a bone surgery patient before and/or after said surgery.
- Particularly valuable members of formula (I) for the purpose of this invention are clodronate, where X and Y both are Cl; pamidronate, where X is OH and Y is
- X and Y are as defined above and M is hydrogen, a pharmaceutically acceptable cation, preferably an alkali metal cation such as sodium or potassium, or an alkyl or aryl moiety, e.g. an alkyl of 1 to 4 carbon atoms or phenyl.
- the compounds of formula (I) or their pharmaceutically acceptable salts and esters can be administered by various routes.
- the suitable administration forms includes systemic use such as oral formulations; parenteral injections including intravenous, intramuscular, intradermal and subcutanous injections; and suppositories.
- the compounds can also be administered locally by laying on or spreading the compounds or compositions thereof directly on the tissue to be treated.
- the required dosage of the compounds of formula (I) or their salts will vary with the particular condition being treated, the severity of the condition, the duration of the treatment, the administration route and the specific bisphosphonate being employed.
- a single daily dose can range from 0.01 to 100 mg per kilogram body weight. Doses higher than 100/kg/day may produce toxic symptoms and should be avoided.
- the preferable bisphosphonate daily doses range from 0.5 to 20 mg/kg.
- the most preferable daily doses are 0.5 to 5 mg/kg.
- For oral administration the preferred daily doses range from 10 to 100 mg/kg.
- a solution of 5 to 100 mg/ml of a biphosphonate should preferably be used before replacement of endo-osteal material.
- the medication should preferably start 1 to 3 weeks before the surgery to obtain the optimal bisphosphonate concentration in bone. After the surgery, the medication should preferably be continued for a period of 1 to 6 months.
- the aim of the study was to determine whether clodronate had a positive effect on vascularization and bone formation in the tibia of a rabbit in which bone was transplanted with the aid of a titanium screw.
- the rabbits were anaesthetized with an i.m. injection of 2.8 mg of Ketalar R (Parke-Davis, Spain) and 2.0 ml of Rompun R (Bayer, Germany) .
- Tibiae were fixed with 5 % phosphate-buffered formalin and toluine blue staining and hematoxylin eosin (HE) were carried out. Specimens were inspected under a light microscope and adverse effects or signs of inflammation were recorded.
- HE hematoxylin eosin
- the vessel count was performed in the specimen where the most vessels were observed. Vessels were counted on two separate occasions by the same observers and the results were averaged. If the variation between two values was greater than 10 %, a third count was undertaken and the three counts were averaged. Vessel counts in both groups were compared using a paired t-test; P values less than 0.05 were considered significant.
- Figure 3 discloses a 21-day specimen from a rabbit treated with clodronate. Implant and transplant are located in the centre of the picture. The donor cavity is seen to the right of the transplant. It can be seen that many vessels penetrate the donor cavity and transplant.
- Figure 4 shows a 21-day specimen from an untreated rabbit. Only a small number of vessels penetrated the transplant.
- Clodronate treated 13.0 4.0 8 The vessels penetrated closer to the centre of the cavity in the medicated rabbits than in the control group. In the medicated rabbits the number of vessels from one side of the specimens was greater than from the opposite side.
- the 14-day control specimens exhibited slight collagen formation and were partly devoid of histologically visible elements in the middle part of the cavity.
- the clodronate- treated specimens exhibited more collagen formation than the control specimens. No empty spaces were seen.
- the control specimens exhibited only slight bone formation at the outer edges of the cavity.
- the inner part of the cavity was mainly filled with collagen and a sharp line between the cavity and bone was clearly seen.
- the clodronate-treated donor cavities were almost completely filled with new bone. Collagen was still found between new bone in the three-week specimens.
- FIG. 5 illustrates a five-week control cavity. Bone regeneration is seen in middle of cavity and in drilling lines. The line between drilled cavity and bone is still seen in most parts of cavity. New bone formation with osteoblasts occurs occasionally in drilling line and also in centre of cavity.
- Figure 6 illustrates a five-week clodronate-treated cavity. Cavity is completely filled with new bone and drilling line is still visible but there is a fusion between donor cavity and cortical bone.
- Figures 7 and 8 represent greater magnifications of Figure 6. In Figure 7 solid new bone and osteoblasts can be observed. Figure 8 shows that cortical and new bone are almost completely fused.
- the soft tissue and periosteum above the transplants contained more collagen in the clodronate-treated group than in the control animals at all stages.
- Fourteen-day control specimens exhibited necrotic bone with invading collagen.
- Treated transplants were beginning to be resorbed at their outer edges.
- Figure 9 represents a side-view of four-week clodronate-treated rabbit's tibia. New bone covers transplant. Periosteum is intact but thinner than that above non-operated area. Implant and transplant are in the middle of this specimen. Donor cavity is to the right from transplant and is the reason for new bone formation in normally empty rabbit's spongious bone.
- a cortical graft is not penetrated by blood vessels until the sixth day (Ray R D; reference as above). Twenty- one days was selected on the basis of the results of a report by Eppley and co-workers (Eppley B et al., J Oral Maxifollfac Surg 1988; 46: 391-98) as bone regeneration time after implantation. They found that the vascularization of bone grafts in rabbits reached a maximum after 21 days.
- the material of this study were 20 edentulous patients. They all came to the Institute of Dentistry, University of Turku, for an implantation procedure. The Institutional Review Board of the Faculty of Medicine at the University of Turku received the project in order to determine whether human subjects are placed at risk. The unanimous decision made by the Institutional Review Board was that the human subjects concerned in this activity would not be placed at any risk. Patients gave permission for an explantation of an extra implant. 10 patients got a daily dose of 1600 mg clodronate disodium until the extra implant was removed (the medicated group) and 10 patients got placebo. The medication and placebo administration, respectively, started one week before the surgery and continued for three weeks after the surgery.
- FIG. 11 is a front view human mandible with four Astra implants, where A means implants, E explanted implant with bone and N is the mandibular nerve. To avoid disturbances in neural function implants are usually placed between the ends of mandibular nerve. At the operation an extra 4 mm screw was installed in the midline of the mandible.
- the 4 mm extra implant was removed with a trephan bore after 4 (10 patients, equally from both groups) and 12 weeks (10 patients, equally from both groups).
- the specimens were imbedded in acrylic blocks and divided in midline in two pieces. To the one piece a histological examination was performed. The other one was taken to a SEM-electromicroscopic examination.
- Electromicroscopic examination in bone-implant interspace and bone in three points with SEM/EDXA (energy dispersive X-ray analysis) was made. At the four different places, two in the upper cortical bone, one in the middle of the implant and one in the bottom of that the following values are calculated: sodium, calcium, phosphor, magnesium and titan. Calcium/phosphor and calcium/magnesium ratio were calculated in 12 points.
- Table III shows the SEM results in human mandibles 4 weeks after implantation of an extra Astra implant. he 10 000 x SEM figure is the same as that in Figures 11 and 12. The exact points where mineral concentrations are measured are shown with small numbers in Figure 14. The mean values of those standard points are given in Table III.
- control 56 30 1.8 1.2 8.2 medicated 72 40 1.8 0.9 2.8
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- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Oral & Maxillofacial Surgery (AREA)
- Biomedical Technology (AREA)
- Pharmacology & Pharmacy (AREA)
- Transplantation (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Dermatology (AREA)
- Cardiology (AREA)
- Organic Chemistry (AREA)
- Vascular Medicine (AREA)
- Molecular Biology (AREA)
- Heart & Thoracic Surgery (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
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- Orthopedic Medicine & Surgery (AREA)
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Abstract
Description
Claims
Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6520683A JPH08510996A (en) | 1993-03-24 | 1994-03-14 | Use of bisphosphonates for bone surgery |
RO95-01658A RO117416B1 (en) | 1993-03-24 | 1994-03-14 | Method of enhancement of bone tissue formation and/or of removal of the late post-surgical complications |
EP94909140A EP0689443B1 (en) | 1993-03-24 | 1994-03-14 | The use of bisphosphonates in bone surgery |
AU62093/94A AU6209394A (en) | 1993-03-24 | 1994-03-14 | The use of bisphosphonates in bone surgery |
DE69427345T DE69427345T2 (en) | 1993-03-24 | 1994-03-14 | USE OF BISPHOSPHONATES IN BONE SURGERY |
DE0689443T DE689443T1 (en) | 1993-03-24 | 1994-03-14 | USE OF BISPHOSPHONATES IN BONE SURGERY |
HK98113017A HK1011926A1 (en) | 1993-03-24 | 1998-12-09 | The use of bisphosphonates in bone surgery |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08/036,140 US5403829A (en) | 1993-03-24 | 1993-03-24 | Use of bisphosphonates in endo-osteal bone surgery |
US08/036,140 | 1993-03-24 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1994021266A1 true WO1994021266A1 (en) | 1994-09-29 |
Family
ID=21886875
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/FI1994/000091 WO1994021266A1 (en) | 1993-03-24 | 1994-03-14 | The use of bisphosphonates in bone surgery |
Country Status (8)
Country | Link |
---|---|
US (1) | US5403829A (en) |
EP (1) | EP0689443B1 (en) |
JP (1) | JPH08510996A (en) |
AU (1) | AU6209394A (en) |
DE (2) | DE689443T1 (en) |
HK (1) | HK1011926A1 (en) |
RO (1) | RO117416B1 (en) |
WO (1) | WO1994021266A1 (en) |
Cited By (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1995028936A1 (en) * | 1994-04-21 | 1995-11-02 | Merck & Co., Inc. | Use of bisphophonates for inhibiting bone resorption following implantation of orthopedic prosthesis |
WO1996023505A1 (en) * | 1995-01-30 | 1996-08-08 | Olli Pekka Teronen | Inhibition of the degradation of connective tissue matrix protein components in mammals |
EP0809502A1 (en) * | 1995-02-17 | 1997-12-03 | Merck & Co., Inc. | Method of lessening the risk of non-vertebral bone fractures |
EP0809503A1 (en) * | 1995-02-17 | 1997-12-03 | Merck & Co., Inc. | Method of lessening the risk of vertebral fractures |
EP0813423A1 (en) * | 1995-01-23 | 1997-12-29 | Xenotech Incorporated | Composition to ameliorate osteolysis and metastasis |
EP0824341A1 (en) * | 1995-05-12 | 1998-02-25 | Merck & Co., Inc. | Prevention of tooth loss by the administration of alendronate or its salts |
US5965547A (en) * | 1994-05-04 | 1999-10-12 | Novartis Corporation | Use of certain methanebishosphonic acid derivatives to prevent prosthesis loosening and prosthesis migration |
WO2000033849A1 (en) * | 1998-12-04 | 2000-06-15 | Roche Diagnostics Gmbh | Use of ibandronate for promoting osseointegration of endoprostheses |
WO2001013922A1 (en) * | 1999-08-19 | 2001-03-01 | The Royal Alexandra Hospital For Children | Drug for treating fractures |
EP1383509A1 (en) * | 2001-04-03 | 2004-01-28 | The Royal Alexandra Hospital for Children | A drug for use in bone grafting |
WO2005074944A1 (en) * | 2004-02-10 | 2005-08-18 | Abiogen Pharma S.P.A. | Use of sodium neridronate to promote new bone formation |
WO2005094784A2 (en) * | 2004-03-31 | 2005-10-13 | Tb Tecnology S.R.L. | Bifunctional bioadhesive compositions for oral implantology |
US7862552B2 (en) | 2005-05-09 | 2011-01-04 | Boston Scientific Scimed, Inc. | Medical devices for treating urological and uterine conditions |
US8882740B2 (en) | 2009-12-23 | 2014-11-11 | Stryker Trauma Gmbh | Method of delivering a biphosphonate and/or strontium ranelate below the surface of a bone |
US9867838B2 (en) | 2009-09-01 | 2018-01-16 | Duke University | Methods for treating heart failure using bisphosphonate compositions |
US9949992B2 (en) | 2011-11-16 | 2018-04-24 | Duke University | Bisphosphonate compositions and methods for treating and\or reducing cardiac dysfunction |
Families Citing this family (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2703590B1 (en) * | 1993-04-05 | 1995-06-30 | Sanofi Elf | USE OF BISPHOSPHONIC ACID DERIVATIVES FOR THE PREPARATION OF MEDICINES FOR PROMOTING BONE REPAIR. |
FI92465C (en) * | 1993-04-14 | 1994-11-25 | Risto Tapani Lehtinen | A method for handling endo-osteal materials |
CA2245793A1 (en) * | 1996-02-14 | 1997-08-21 | Itzhak Binderman | Topical bisphosphonates for prevention of bone resorption |
US6117856A (en) * | 1996-02-14 | 2000-09-12 | Binderman; Itzhak | Topical bisphosphonates for prevention of bone resorption |
US6376476B1 (en) | 1996-12-13 | 2002-04-23 | Zymogenetics Corporation | Isoprenoid pathway inhibitors for stimulating bone growth |
US6555529B1 (en) * | 1997-12-25 | 2003-04-29 | Toray Industries, Inc. | Remedies for intramedullary diseases |
JP2002525323A (en) * | 1998-09-25 | 2002-08-13 | スノル・モレキュラー・コーポレーション | Pharmaceutical active compounds and methods of using the same |
US5998390A (en) * | 1998-09-28 | 1999-12-07 | The Research Foundation Of State University Of New York | Combination of bisphosphonate and tetracycline |
US6794536B1 (en) | 1998-12-10 | 2004-09-21 | Aesqen, Inc. | Method for preparation of disodium pamidronate |
US6160165A (en) * | 1998-12-10 | 2000-12-12 | Aesgen, Inc. | Method for preparation of disodium pamidronate |
ATE301129T1 (en) | 1999-05-04 | 2005-08-15 | Strakan Int Ltd | ANDROGEN GLYCOSIDES AND THE ANDROGENIC ACTIVITY THEREOF |
CA2308532C (en) * | 1999-05-12 | 2005-11-29 | Gador S.A. | Use of bisphosphonates for the treatment of osteogenesis imperfecta |
EP1267888A4 (en) * | 2000-01-04 | 2005-12-28 | Univ California | Use of low dosage bisphosphonates to inhibit cardiac and arterial calcification |
WO2001051497A1 (en) * | 2000-01-14 | 2001-07-19 | Strakan Limited | Novel bisphosphonates and uses thereof |
US7425549B2 (en) * | 2001-02-06 | 2008-09-16 | The Royal Alexandra Hospital For Children | Drug for the treatment of osteonecrosis and for the management of patients at risk of developing osteonecrosis |
CA2372450A1 (en) * | 2001-05-10 | 2001-09-19 | Pharmaceutical Partners Of Canada Inc. | Liquid injectable formulation of disodium pamidronate |
US7041309B2 (en) * | 2002-06-13 | 2006-05-09 | Neuropro Technologies, Inc. | Spinal fusion using an HMG-CoA reductase inhibitor |
US8071574B2 (en) * | 2005-02-22 | 2011-12-06 | John Dennis Bobyn | Implant improving local bone formation |
US7914810B2 (en) * | 2005-05-06 | 2011-03-29 | Synthes Usa, Llc | Methods for the in situ treatment of bone cancer |
DE102005053512A1 (en) * | 2005-11-09 | 2007-06-28 | Omnimedic Gbr | Use of clodronic acid for the treatment of podotrochlosis |
US20100144679A1 (en) * | 2007-03-21 | 2010-06-10 | Duke University | Medication kits and formulations for preventing, treating or reducing secondary fractures after previous fracture |
Citations (1)
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US4753652A (en) * | 1984-05-04 | 1988-06-28 | Children's Medical Center Corporation | Biomaterial implants which resist calcification |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
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US4067971A (en) * | 1976-05-13 | 1978-01-10 | The Procter & Gamble Company | Therapeutic composition |
DE2813121A1 (en) * | 1977-03-29 | 1978-10-12 | Procter & Gamble | Di:chloromethane di:phosphonate compsns. - for stimulating collagen formation and treating of healing wounds and rheumatic and allied disorders |
US5227506A (en) * | 1989-09-06 | 1993-07-13 | Merck & Co., Inc. | Acyloxymethyl esters of bisphosphonic acids as bone resorption inhibitors |
US5270365A (en) * | 1991-12-17 | 1993-12-14 | Merck & Co., Inc. | Prevention and treatment of periodontal disease with alendronate |
-
1993
- 1993-03-24 US US08/036,140 patent/US5403829A/en not_active Expired - Lifetime
-
1994
- 1994-03-14 WO PCT/FI1994/000091 patent/WO1994021266A1/en active IP Right Grant
- 1994-03-14 RO RO95-01658A patent/RO117416B1/en unknown
- 1994-03-14 DE DE0689443T patent/DE689443T1/en active Pending
- 1994-03-14 JP JP6520683A patent/JPH08510996A/en not_active Ceased
- 1994-03-14 DE DE69427345T patent/DE69427345T2/en not_active Expired - Lifetime
- 1994-03-14 AU AU62093/94A patent/AU6209394A/en not_active Abandoned
- 1994-03-14 EP EP94909140A patent/EP0689443B1/en not_active Expired - Lifetime
-
1998
- 1998-12-09 HK HK98113017A patent/HK1011926A1/en not_active IP Right Cessation
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Also Published As
Publication number | Publication date |
---|---|
AU6209394A (en) | 1994-10-11 |
DE69427345T2 (en) | 2002-05-02 |
JPH08510996A (en) | 1996-11-19 |
DE69427345D1 (en) | 2001-07-05 |
HK1011926A1 (en) | 1999-07-23 |
EP0689443B1 (en) | 2001-05-30 |
EP0689443A1 (en) | 1996-01-03 |
US5403829A (en) | 1995-04-04 |
RO117416B1 (en) | 2002-03-29 |
DE689443T1 (en) | 1996-10-24 |
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