US2014271735A1PendingUtilityA1
Use of calcitonin in osteoarthritis
Est. expiryJul 23, 2023(expired)· nominal 20-yr term from priority
A61P 19/10A61P 1/08A61P 19/08A61P 19/02A61P 19/00A61K 9/0043A61K 9/2054A61K 47/16A61K 47/56A61K 9/0031A61K 47/183A61K 38/23A61K 45/06A61K 9/2013A61K 47/48169
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Claims
Abstract
The present invention relates to a novel use of calcitonin in osteoarthritis, and to methods of treating and/or preventing osteoarthritis in mammals, particularly humans.
Claims
exact text as granted — not AI-modified1 . A method of preventing or/and treating osteoarthritis in a patient in need thereof comprising administering to said patient a therapeutically effective amount of a calcitonin in free or salt form.
2 . A method of inhibiting resorption and/or normalizing turnover of subchondral bone in a patient in need thereof comprising administering to said patient a therapeutically effective amount of a calcitonin in free or salt form.
3 . The method according to claim 2 , wherein the therapeutically effective amount of a calcitonin is delivered orally.
4 . The method according to claim 2 , wherein the therapeutically effective amount of a calcitonin is delivered orally in a composition comprising the calcitonin and a delivery agent for calcitonin.
5 . The method according to claim 2 , wherein the therapeutically effective amount of a calcitonin is delivered orally in a composition comprising the calcitonin which is conjugated to a polymer molecule.
6 . The method according to claim 2 , wherein the therapeutically effective amount of a calcitonin is delivered with an effective dosage of an oral pharmaceutical composition comprising calcitonin, at least one pharmaceutically acceptable pH-lowering agent, at least one absorption enhancer, and an enteric coating.
7 . The method according to claim 4 , wherein the calcitonin is a salmon calcitonin.
8 . The method of claim 4 , whereas said pharmaceutical composition comprises a delivery agent selected from the group of 5-CNAC, SNAD, and SNAC.
9 . The method according to claim 4 , whereas said pharmaceutical composition comprises a delivery agent selected from the group consisting of a disodium salt of 5-CNAC, a disodium salt of SNAD, and a disodium salt of SNAC.
10 . The method according to claim 4 , whereas said pharmaceutical composition comprises a delivery agent in micronized form.
11 . A pharmaceutical composition for use in the treatment or/and prevention of osteoarthritis in a patient in need thereof, comprising a calcitonin together with one or more pharmaceutically acceptable diluents or carriers therefore.
12 . A pharmaceutical combination for use in the treatment or/and prevention of osteoarthritis in a patient in need thereof, comprising:
a) a first agent which is a calcitonin, and b) a co-agent which is a bone resorption inhibitor, bone forming drug or pain reducing agent.
13 . The pharmaceutical composition of claim 12 comprising between 0.4 and 2.5 mg of a calcitonin.Cited by (0)
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