US2012316217A1PendingUtilityA1
combination for the treatment of osteoarthritis
Est. expiryDec 21, 2029(~3.4 yrs left)· nominal 20-yr term from priority
Inventors:Franco ContiEdoardo ContiGiovanni Federico Maria ContiArborio Mella IsabellaFrancesco Saverio Dioguardi
A61P 43/00A61P 19/02A61P 19/00A61K 31/717A61L 2300/40A61K 31/728A61L 27/54A61K 31/401A61K 31/79A61K 9/0019A61K 45/06A61K 47/36A61K 31/198
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Claims
Abstract
The present invention relates to the use of a combination of glycine, proline, and optionally a natural or synthetic viscosity-controlling polymer, and/or lysine and/or leucine, to prepare a composition for the treatment of osteoarthritis.
Claims
exact text as granted — not AI-modified1 . An intra-articular formulation for the treatment of osteoarthritis comprising:
a) glycine, b) proline, and optionally c) a natural or synthetic viscosity-controlling polymer, and/or d) lysine, and/or e) leucine.
2 . The formulation as claimed in claim 1 , wherein osteoarthritis is patellofemoral or femorotibial knee osteoarthritis, hip osteoarthritis and shoulder osteoarthritis.
3 . The formulation as claimed in claim 1 , wherein the natural or synthetic viscosity-controlling polymer is selected from hyaluronic acid or a salt thereof, polyvinylpyrrolidone and cellulose derivatives.
4 . The formulation as claimed in claim 3 , wherein the natural or synthetic viscosity-controlling polymer is hyaluronic acid or a salt thereof.
5 . The formulation as claimed in claim 1 , wherein the amino acids are in L form.
6 . The formulation as claimed in claim 1 , wherein the various components of the combination are present in the following ranges by weight:
a) 25 to 500 mg of glycine, b) 40 to 300 mg of proline, and optionally c) 5 to 50 mg of hyaluronic acid or a salt thereof, and/or d) 5 to 100 mg of lysine, and/or e) 5 to 50 mg of leucine.
7 . The formulation as claimed in claim 1 , in the form of powders for reconstitution or viscous solutions in biocompatible solvents.Cited by (0)
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