WO2002049639A1 - Use of isovaleryl l-carnitine for the preparation of a medicament for the prevention and cure of osteoporosis - Google Patents

Use of isovaleryl l-carnitine for the preparation of a medicament for the prevention and cure of osteoporosis Download PDF

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Publication number
WO2002049639A1
WO2002049639A1 PCT/IT2001/000614 IT0100614W WO0249639A1 WO 2002049639 A1 WO2002049639 A1 WO 2002049639A1 IT 0100614 W IT0100614 W IT 0100614W WO 0249639 A1 WO0249639 A1 WO 0249639A1
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WO
WIPO (PCT)
Prior art keywords
carnitine
acid
osteoporosis
fumarate
isovaleryl
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Ceased
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PCT/IT2001/000614
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French (fr)
Inventor
Aleardo Koverech
Alberta Zallone
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Sigma Tau Industrie Farmaceutiche Riunite SpA
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Sigma Tau Industrie Farmaceutiche Riunite SpA
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Priority to AT01271219T priority Critical patent/ATE301998T1/en
Priority to AU2002217431A priority patent/AU2002217431A1/en
Priority to MXPA03006332A priority patent/MXPA03006332A/en
Priority to US10/470,158 priority patent/US6906102B2/en
Priority to DK01271219T priority patent/DK1351676T3/en
Priority to DE60112802T priority patent/DE60112802T2/en
Priority to EP01271219A priority patent/EP1351676B1/en
Priority to SK891-2003A priority patent/SK287306B6/en
Application filed by Sigma Tau Industrie Farmaceutiche Riunite SpA filed Critical Sigma Tau Industrie Farmaceutiche Riunite SpA
Priority to CA2434962A priority patent/CA2434962C/en
Priority to HU0400735A priority patent/HU227342B1/en
Publication of WO2002049639A1 publication Critical patent/WO2002049639A1/en
Anticipated expiration legal-status Critical
Priority to US11/032,019 priority patent/US7084174B2/en
Ceased legal-status Critical Current

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    • 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
    • A61K31/21—Esters, e.g. nitroglycerine, selenocyanates
    • A61K31/215—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
    • A61K31/22—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin
    • A61K31/221—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin with compounds having an amino group, e.g. acetylcholine, acetylcarnitine
    • 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
    • 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
    • A61P19/04—Drugs for skeletal disorders for non-specific disorders of the connective tissue
    • 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

Definitions

  • isovaleryl L-carnitine for the preparation of a medicament for the prevention and cure of osteoporosis.
  • the present invention relates to the use of isovaleryl L- carnitine for the preparation of a medicament for the prevention and cure of osteoporosis, for the prevention and cure of fractures occurring during post-menopause osteoporosis or during ageing.
  • Aged people or people which are in post-menopause are subjected to fractures due to the fragility of the bone caused by osteoporosis.
  • the hospitalisation period of patients with bone fractures which may last some day or some months, depends from the type of fracture, the age, and from the general conditions of the patients.
  • the convalescence period depends on the gravity of the pathology. At the end of this period patients come back to the hospital for the radiographic controls of the bony callus formation.
  • WO 98/46233 describes a pharmaceutical compositions comprising an alkanoyl L-carnitine in combination with the dehydroepiandrosterone (DHEA) or the dehydroepiandrosterone sulphate (DHEA-S) capable to stimulate the multiplication and growth of the osteoblast.
  • DHEA dehydroepiandrosterone
  • DHEA-S dehydroepiandrosterone sulphate
  • WO 99/66913 describes compositions useful for the treatment of the osteoporosis and menopausal syndromes which comprise propionyl L-carnitine in combination with 4'-5,7-trihydroxiflavone.
  • the patent FR 2765804 describes compositions useful for the treatment of osteoporosis containing calcium pidolate, calcium carbonate, and carnitine.
  • WO 98/01128 describes the use of acetyl L-carnitine, isovaleryl L-carnitine and propionyl L-carnitine for increasing the IGF- 1 levels for the treatment and prevention of cytological disorders and pathologies related to IGF 1.
  • WO 95/05168 describes an oral medicament at controlled release comprising carnitine, which does not causes gastrointestinal irritation, for the treatment of the osteoporosis.
  • mice treated with L-carnitine increase the production of osteocalcine (index of better calcification), while in the same animals the treatment with acetyl L-carnitine reduces the production of this marker during the formation of the bone matrix.
  • isovaleryl L-carnitine shows to be more active than L-carnitine, or as active as, but a doses less than 10 or 20 times, respect to L- carnitine. Is therefore object of the present invention the use of isovaleryl
  • Non-limiting examples of suitable salts include the chloride, bromide, orotate, acid aspartate, acid citrate, magnesium citrate, acid phosphate, fumarate, acid fumarate, magnesium fumarate, lactate, maleate, acid maleate, mucate, acid oxalate, pamoate, acid pamoate, acid sulphate, glucose phosphate, tartrate, acid tartrate, magnesium tartrate, 2-amino etanesulfonate, magnesium 2-amino etariesulfonate, coline tartrate and trichloroacetate.
  • the compound according to the present invention can be administered to patients in need, either alone or in concomitance with vitamins, mineral salts and/ or other known drugs useful for the treatment of osteoporosis and fractures during osteoporosis.
  • vitamins, mineral salts and/ or other known drugs useful for the treatment of osteoporosis and fractures during osteoporosis can be administered to patients in need, either alone or in concomitance with vitamins, mineral salts and/ or other known drugs useful for the treatment of osteoporosis and fractures during osteoporosis.
  • the following example illustrate the invention. EXAMPLE Preparation of the human osteoblasts
  • the differentiated human osteoblasts were prepared starting from bone fragments obtained during surgical operation following the procedure described in Calcif. Tissue Int. 62: 362-365, 1998; and in Calcif. Tissue Int. 37: 453-460, 1985.
  • bone fragments were undertaken to enzymatic digestion with collagenase (1 mg/ml) diluted in phosphate buffer in order to remove fibroblasts, haematic endothelial cells or bone marrow cells, if any.
  • the fragments so cleaned were maintained in culture in presence of a medium containing 20% of foetal calf serum (FCS) to obtain osteoblasts population for explant.
  • FCS foetal calf serum
  • the cells so obtained were characterised to verify their osteoblastic phenotype then used for the experiments.
  • the cellular proliferation test was done growing the cells in 96 well plates, in medium without FCS, and with bovine serum albumin (BSA).
  • BSA bovine serum albumin
  • the cells were exposed to increasing doses of L-carnitine fumarate and isovaleryl L-carnitine fumarate.
  • the positive control group was constituted by cells growing in presence of FCS (15%).
  • samples from plates in culture were fixed with a solution of paraformaldehyde at 3%, the cells were stained with crystal- violet at 0,5%, washed to eliminate the excess of stain and a solution of sodium citrate 0, 1 M in ethanol was added.
  • the number of the cells contained in the wells was evaluated by colorimetric test at 540 nm.
  • Figure 2 (L-carnitine fumarate) shown that isovaleryl L-carnitine fumarate induces cells proliferation (Figure 1) in a more potent way, if compared with the cells proliferation induced by L-carnitine fumarate ( Figure 2).
  • the collagen production represents a method for the evaluation of the osteoblast activity.
  • isovaleryl L-carnitine shows to be more active in some experiments, and as active as, at doses at least 10 times lower, also respect to the reference compound (L-carnitine).
  • the statistical analysis of all the results was made using the Student "t" test.
  • the amount of the drug to be administered to patients in need will be decided by the physician on the base of the age, weight and general conditions of the patient.
  • the unitary dosage to be administered will be about 0,5-3 g/day, preferably 1-2 g/day, in solid form, powder, granular or liposomic in pills, capsules, granulates, powder, vials for oral, parenteral, rectal or topic use.
  • These administration forms may further contain vitamins, mineral salts, and/or other known drugs useful for the treatment of the osteoporosis and fractures during osteoporosis.

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Chemical & Material Sciences (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Engineering & Computer Science (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Epidemiology (AREA)
  • Emergency Medicine (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Rheumatology (AREA)
  • Biomedical Technology (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Coloring Foods And Improving Nutritive Qualities (AREA)

Abstract

The use of isovaleryl L-carnitine for the preparation of a medicament for the prevention and cure of osteoporosis and for the prevention and cure of fractures occurring during osteoporosis post-menopause or during the ageing, is described.

Description

Use of isovaleryl L-carnitine for the preparation of a medicament for the prevention and cure of osteoporosis.
The present invention relates to the use of isovaleryl L- carnitine for the preparation of a medicament for the prevention and cure of osteoporosis, for the prevention and cure of fractures occurring during post-menopause osteoporosis or during ageing.
Aged people or people which are in post-menopause are subjected to fractures due to the fragility of the bone caused by osteoporosis. The hospitalisation period of patients with bone fractures, which may last some day or some months, depends from the type of fracture, the age, and from the general conditions of the patients.
The convalescence period depends on the gravity of the pathology. At the end of this period patients come back to the hospital for the radiographic controls of the bony callus formation.
Unfortunately not all patients present the same degree of recovery, in fact some of them present a minor, some time a complete lack of bony callus formation. Because of these events patients are obliged to remain inactive for a further period of time, with a loss of working day and an increases of the hospital expenses.
To date exist few specific therapeutical compounds which act directly on the bone cells, the osteoblasts, favouring in a specific way their propagation with formation of bony callus and wound healing.
In the orthopaedic section of the hospital, as adjuvant therapy of the fractures are used calcitonine or alendronates, drugs specific for the prevention of the post-menopausal osteoporosis, eventually in combination with vitamins, particularly with vitamin D and mineral salts, which act limiting the osteoclastic activity.
Therefor, the discovery of new drugs which exert their action directly on the osteoblasts and are capable both to support their multiplication and the bony callus formation, and to decrease the recovering period, would have a beneficial effect on the patients.
Considering the relevant number of patients involved, it is evident both the socio-economics benefit obtainable, reducing the hospital expenses, increasing the working day during the year, and particularly improving the quality life' of the patients.
Is therefore the scope of the present invention to furnish a drug, which overcoming the drawbacks and the unsatisfactory efficacy of the therapeutical compounds used to date, is capable to limits the osteoclastic activity accelerating the formation of bony matrix (stimulating the osteoblastic activity) and is an useful agent for the prevention and treatment of osteoporosis.
Compounds useful for the cure of fractures and osteoporosis are already known. WO 98/46233 describes a pharmaceutical compositions comprising an alkanoyl L-carnitine in combination with the dehydroepiandrosterone (DHEA) or the dehydroepiandrosterone sulphate (DHEA-S) capable to stimulate the multiplication and growth of the osteoblast. WO 99/66913 describes compositions useful for the treatment of the osteoporosis and menopausal syndromes which comprise propionyl L-carnitine in combination with 4'-5,7-trihydroxiflavone.
The patent FR 2765804 describes compositions useful for the treatment of osteoporosis containing calcium pidolate, calcium carbonate, and carnitine.
WO 98/01128 describes the use of acetyl L-carnitine, isovaleryl L-carnitine and propionyl L-carnitine for increasing the IGF- 1 levels for the treatment and prevention of cytological disorders and pathologies related to IGF 1.
WO 95/05168 describes an oral medicament at controlled release comprising carnitine, which does not causes gastrointestinal irritation, for the treatment of the osteoporosis.
In Journal of Pharmaceutical Sciences Vol. 84; N° 4; April 1995 is described the use of long chain acyl carnitine ester in racemic form (palmitoyl-carnitine, miristoyl-carnitine and lauroyl-carnitine), as useful agent for the prevention of the osteoporosis.
In "Comptes rendus des seances de la Societe de Biologie. Seance du 27 Juin 1964.- Tome CLVIII, n 6, 1964, p. 1410" is reported that in rat the use of D, L-carnitine increases the bone calcium.
In The Journal of Rheumatology 1999, 26; 2229-32 is described the use of carnitine, in subject adult, for the treatment of the hip fracture. In Revue Agressologie 1963 - IV., 4, is described the use of carnitine during the growth or following fractures.
In Gerontologist, (9), 32-33, 1992 is reported that in mice treated with L-carnitine increase the production of osteocalcine (index of better calcification), while in the same animals the treatment with acetyl L-carnitine reduces the production of this marker during the formation of the bone matrix.
None of the above cited publications teach or suggest the use of isovaleryl L-carnitine for the preparation of a medicament for the treatment of osteoporosis.
Moreover, the cited publication on Gerontologist gives a severe technical prejudice on the use of a short chain alkanoyl L-carnitines for promoting the production of bone matrix, in fact it is reported that acetyl L-carnitine to reduces the production of osteocalcine. It has surprisingly been found that isovaleryl L-carnitine promotes the formation and proliferation of osteoblasts and is a therapeutic agent useful for the prevention and treatment of osteoporosis and for the prevention and treatment of fractures during post-menopausal osteoporosis or secondary to elderly. The experimental data, in the following reported, show that the compound according to the invention promotes cells proliferation and collagen production in human osteoblastic cells in vitro. In fact, isovaleryl L-carnitine shows to be more active than L-carnitine, or as active as, but a doses less than 10 or 20 times, respect to L- carnitine. Is therefore object of the present invention the use of isovaleryl
L-carnitine or a pharmacological acceptable salt thereof, for preparing a medicament useful for increasing the healing of fractures and useful for the prevention and treatment of osteoporosis.
For pharmaceutically acceptable salt of isovaleryl L-carnitine is intended any salts of this with an acid which does not give rise to undesirable toxic or side effects.
This acids are well known to the experts in pharmacy and pharmaceutical technology.
Non-limiting examples of suitable salts include the chloride, bromide, orotate, acid aspartate, acid citrate, magnesium citrate, acid phosphate, fumarate, acid fumarate, magnesium fumarate, lactate, maleate, acid maleate, mucate, acid oxalate, pamoate, acid pamoate, acid sulphate, glucose phosphate, tartrate, acid tartrate, magnesium tartrate, 2-amino etanesulfonate, magnesium 2-amino etariesulfonate, coline tartrate and trichloroacetate.
Preferred is isovaleryl L-carnitine fumarate.
The compound according to the present invention can be administered to patients in need, either alone or in concomitance with vitamins, mineral salts and/ or other known drugs useful for the treatment of osteoporosis and fractures during osteoporosis. The following example illustrate the invention. EXAMPLE Preparation of the human osteoblasts
The differentiated human osteoblasts were prepared starting from bone fragments obtained during surgical operation following the procedure described in Calcif. Tissue Int. 62: 362-365, 1998; and in Calcif. Tissue Int. 37: 453-460, 1985.
In short, bone fragments were undertaken to enzymatic digestion with collagenase (1 mg/ml) diluted in phosphate buffer in order to remove fibroblasts, haematic endothelial cells or bone marrow cells, if any.
The fragments so cleaned were maintained in culture in presence of a medium containing 20% of foetal calf serum (FCS) to obtain osteoblasts population for explant. The cells so obtained were characterised to verify their osteoblastic phenotype then used for the experiments. Cellular proliferation test
The cellular proliferation test was done growing the cells in 96 well plates, in medium without FCS, and with bovine serum albumin (BSA).
The cells were exposed to increasing doses of L-carnitine fumarate and isovaleryl L-carnitine fumarate. The positive control group was constituted by cells growing in presence of FCS (15%).
Every 24 ore, for 5 days, samples from plates in culture were fixed with a solution of paraformaldehyde at 3%, the cells were stained with crystal- violet at 0,5%, washed to eliminate the excess of stain and a solution of sodium citrate 0, 1 M in ethanol was added.
The number of the cells contained in the wells was evaluated by colorimetric test at 540 nm. The results obtained, reported in Figure 1, shows that isovaleryl L-carnitine fumarate promotes cells proliferation.
Moreover, the results obtained reported in Figure 1 (isovaleryl
L-carnitine fumarate) in comparison with the results reported in
Figure 2 (L-carnitine fumarate) shown that isovaleryl L-carnitine fumarate induces cells proliferation (Figure 1) in a more potent way, if compared with the cells proliferation induced by L-carnitine fumarate (Figure 2).
In fact, it is worthy of note that in Figure 1 isovaleryl L- carnitine fumarate at a dose (10 3 M) 10 times lower than that of L- carnitine fumarate (10~2 M) has the same cellular proliferation activity compared to the activity of L-carnitine fumarate (Figure 2).
The statistical analysis of the results was made using the Student "t" test.
Production of collagen by incorporation of 3H-proline The collagen production represents a method for the evaluation of the osteoblast activity.
This production was evaluated on semiconfluent cells grown on
24 wells plates, in medium without serum (FCS) containing 1 μCi/well of 3H-proline, both in the wells of the control and in the wells where were present the tested compounds. After 4 hours of incubation in presence of the tracer the cells were lysed and undertaken to an extraction procedure (Journal of Bone and Mineral Research, 2000; Vol. 15(2); 188-97). The cells were washed with phosphate buffer (PBS) dissolved in 0,5 ml/ well of sodium dodecyl sulphate at 10% and undergone to precipitation for 30 minutes at 4°C by the addition of sulphate trichloroacetic acid at 3%. The radioactivity of the cells, as index of the cells collagen synthesis, was evaluated with a beta-counter.
The results obtained reported in Figure 3 shown that isovaleryl L-carnitine fumarate increases the production of collagen in an higher way respect to the control sample, in which the tested compound was absent.
Moreover, the results obtained reported in Figure 3 shown that isovaleryl L-carnitine fumarate has a favouring activity for the production of collagen in a significant way respect to the same doses of L-carnitine fumarate. The statistical analysis of the results was made using the Student "t" test.
As above mentioned, the results obtained shown that the compound according to the present invention promotes in a statistical significant way the proliferation and the collagen production in human osteoblastic cells in vitro respect to the control samples, in which said compounds was absent. Moreover, isovaleryl L-carnitine shows to be more active in some experiments, and as active as, at doses at least 10 times lower, also respect to the reference compound (L-carnitine). The statistical analysis of all the results was made using the Student "t" test.
The amount of the drug to be administered to patients in need will be decided by the physician on the base of the age, weight and general conditions of the patient.
However, the unitary dosage to be administered will be about 0,5-3 g/day, preferably 1-2 g/day, in solid form, powder, granular or liposomic in pills, capsules, granulates, powder, vials for oral, parenteral, rectal or topic use. These administration forms may further contain vitamins, mineral salts, and/or other known drugs useful for the treatment of the osteoporosis and fractures during osteoporosis.

Claims

1. Use of isovaleryl L-carnitine or a pharmaceutical acceptable salt thereof for preparing a medicament for the prevention and treatment of osteoporosis.
2. Use according to claim 1, for the prevention and treatment of fractures during osteoporosis.
3. Use according to claim 1, or 2, in which the pharmaceutical acceptable salt is selected from the group consisting of: chloride, bromide, orotate, acid aspartate, acid citrate, magnesium citrate, acid phosphate, fumarate, acid fumarate, magnesium fumarate, lactate, maleate, acid maleate, mucate, acid oxalate, pamoate, acid pamoate, acid sulphate, glucose phosphate, tartrate, acid tartrate, magnesium tartrate, 2-amino etanesulfonate, magnesium 2-amino etanesulfonate, coline tartrate and trichloroacetate.
4. Use according to claims 1-3, in which the saltTis fumarate.
5. Use according to any preceding claims further comprising vitamins, mineral salts and/ or other known drugs useful for the treatment of osteoporosis and fractures during osteoporosis.
PCT/IT2001/000614 2000-12-21 2001-12-04 Use of isovaleryl l-carnitine for the preparation of a medicament for the prevention and cure of osteoporosis Ceased WO2002049639A1 (en)

Priority Applications (11)

Application Number Priority Date Filing Date Title
EP01271219A EP1351676B1 (en) 2000-12-21 2001-12-04 Use of isovaleryl l-carnitine for the preparation of a medicament for the prevention and cure of osteoporosis
MXPA03006332A MXPA03006332A (en) 2000-12-21 2001-12-04 Use of isovaleryl l-carnitine for the preparation of a medicament for the prevention and cure of osteoporosis.
US10/470,158 US6906102B2 (en) 2000-12-21 2001-12-04 Use of isovaleryl L-carnitine to increase healing of bone fractures
DK01271219T DK1351676T3 (en) 2000-12-21 2001-12-04 Use of isovaleryl-L-carnitine in the manufacture of a drug for the prevention and treatment of fractures
DE60112802T DE60112802T2 (en) 2000-12-21 2001-12-04 USE OF ISOVALERYL-L-CARNITINE FOR THE MANUFACTURE OF A MEDICAMENT FOR PREVENTING AND THERAPY OF OSTEOPOROSIS
AT01271219T ATE301998T1 (en) 2000-12-21 2001-12-04 USE OF ISOVALERYL-L-CARNITINE FOR THE PRODUCTION OF A MEDICINAL PRODUCT FOR THE PREVENTION AND TREATMENT OF OSTEOPOROSIS
HU0400735A HU227342B1 (en) 2000-12-21 2001-12-04 Use of isovaleryl l-carnitine for the preparation of a medicament for the prevention and cure of osteoporosis
SK891-2003A SK287306B6 (en) 2000-12-21 2001-12-04 Use of isovaleryl L-carnitine for the preparation of a medicament for the prevention and treatment of fractures
CA2434962A CA2434962C (en) 2000-12-21 2001-12-04 Use of isovaleryl l-carnitine for the treatment of fractures
AU2002217431A AU2002217431A1 (en) 2000-12-21 2001-12-04 Use of isovaleryl l-carnitine for the preparation of a medicament for the prevention and cure of osteoporosis
US11/032,019 US7084174B2 (en) 2000-12-21 2005-01-11 Administration of isovaleryl L-carnitine to stimulate osteoblastic activity

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
ITRM2000A000688 2000-12-21
IT2000RM000688A IT1317079B1 (en) 2000-12-21 2000-12-21 USE OF ISOVALERIL L-CARNITINE FOR THE PREPARATION OF A MEDICATION FOR THE PREVENTION AND TREATMENT OF OSTEOPOROSIS.

Related Child Applications (2)

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US10470158 A-371-Of-International 2001-12-04
US11/032,019 Division US7084174B2 (en) 2000-12-21 2005-01-11 Administration of isovaleryl L-carnitine to stimulate osteoblastic activity

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US (2) US6906102B2 (en)
EP (1) EP1351676B1 (en)
AT (1) ATE301998T1 (en)
AU (1) AU2002217431A1 (en)
CA (1) CA2434962C (en)
CZ (1) CZ304356B6 (en)
DE (1) DE60112802T2 (en)
DK (1) DK1351676T3 (en)
ES (1) ES2247005T3 (en)
HU (1) HU227342B1 (en)
IT (1) IT1317079B1 (en)
MX (1) MXPA03006332A (en)
PL (1) PL207879B1 (en)
SK (1) SK287306B6 (en)
WO (1) WO2002049639A1 (en)

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1998001128A1 (en) * 1996-07-05 1998-01-15 Mendes S.R.L. Use of l-acetylcarnitine, l-isovalerylcarnitine, l-propionylcarnitine for increasing the levels of igf-1
WO1999066913A2 (en) * 1998-06-23 1999-12-29 Sigma-Tau Healthscience S.P.A. Composition for the prevention and/or treatment of osteoporosis and alterations due to menopause syndrome, comprising propionyl-l-carnitine and genistein

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IT1291141B1 (en) * 1997-04-16 1998-12-29 Sigma Tau Ind Farmaceuti PHARMACEUTICAL COMPOSITION INCLUDING AN ALCANOYL L-CARNITINE, SUITABLE TO STIMULATE THE MULTIPLICATION AND GROWTH OF OSTEOBLASTS

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1998001128A1 (en) * 1996-07-05 1998-01-15 Mendes S.R.L. Use of l-acetylcarnitine, l-isovalerylcarnitine, l-propionylcarnitine for increasing the levels of igf-1
WO1999066913A2 (en) * 1998-06-23 1999-12-29 Sigma-Tau Healthscience S.P.A. Composition for the prevention and/or treatment of osteoporosis and alterations due to menopause syndrome, comprising propionyl-l-carnitine and genistein

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IT1317079B1 (en) 2003-05-26
SK8912003A3 (en) 2003-11-04
PL207879B1 (en) 2011-02-28
ITRM20000688A0 (en) 2000-12-21
ES2247005T3 (en) 2006-03-01
EP1351676B1 (en) 2005-08-17
DK1351676T3 (en) 2005-12-19
HU227342B1 (en) 2011-04-28
SK287306B6 (en) 2010-06-07
EP1351676A1 (en) 2003-10-15
CA2434962C (en) 2010-02-09
CA2434962A1 (en) 2002-06-27
MXPA03006332A (en) 2004-04-21
US20040077718A1 (en) 2004-04-22
US20050143458A1 (en) 2005-06-30
HUP0400735A3 (en) 2009-01-28
CZ304356B6 (en) 2014-03-26
DE60112802T2 (en) 2006-03-16
ITRM20000688A1 (en) 2002-06-21
HUP0400735A2 (en) 2004-07-28
DE60112802D1 (en) 2005-09-22
US6906102B2 (en) 2005-06-14
CZ20031890A3 (en) 2004-04-14
US7084174B2 (en) 2006-08-01
PL367293A1 (en) 2005-02-21
ATE301998T1 (en) 2005-09-15
AU2002217431A1 (en) 2002-07-01

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