IP Library Granted Patent US 7,585,896
Granted Patent B2
US 7,585,896 · App. 10/667,482 · Granted Sep 8, 2009

Composition for the prevention and treatment of kidney dysfunctions and diseases

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Quick Facts
Patent No.
US 7,585,896
App. No.
10/667,482
Granted
Sep 8, 2009
Kind
B2
Abstract

A composition is disclosed which is suitable for the prevention and treatment of kidney dysfunctions and diseases and which can therefore take the form of a food supplement or of an actual medicinal drug comprising a combination of acetyl L-carnitine and propionyl L-carnitine or their pharmacologically acceptable salts.

Claims (9)

1. A method for providing kidney protection from a kidney dysfunction caused by lithium which comprises administering to an individual in need thereof a therapeutically effective amount of acetyl L-carnitine and propionyl L-carnitine or a pharmacologically acceptable salt thereof, in which the weight-ratio of acetyl L-carnitine to propionyl L-carnitine is 1:1.

2. A method for providing protection from a kidney dysfunction caused by lithium which comprises administering to an individual in need thereof a combination composition of a therapeutically effective amount of acetyl L-carnitine and propionyl L-carnitine or a pharmacologically acceptable salt thereof, in which the weight-ratio of acetyl L-carnitine to propionyl L-carnitine is 1:1.

3. A method for providing protection from nephropathy caused by lithium which comprises administering to an individual in need thereof a combination composition of a therapeutically effective amount of acetyl L-carnitine and propionyl L-carnitine or a pharmacologically acceptable salt thereof, in which the weight-ratio of acetyl L-carnitine to propionyl L-carnitine is 1:1.

4. A method for providing protection from tubular necrosis caused by lithium which comprises administering to an individual in need thereof a therapeutically effective amount of a combination composition of a therapeutically effective amount of acetyl L-carnitine and propionyl L-carnitine or a pharmacologically acceptable salt thereof, in which the weight-ratio of acetyl L-carnitine to propionyl L-carnitine is 1:1.

5. A method for providing protection from tubular necrosis caused by lithium which comprises administering to an individual in need thereof a therapeutically effective amount of acetyl L-carnitine and propionyl L-carnitine or a pharmacologically acceptable salt thereof, in which the weight-ratio of acetyl L-carnitine to propionyl L-carnitine is 1:1.

6. A method for providing protection from tubular necrosis caused by lithium which comprises administering to an individual in need thereof 2-5 mg/kg body weight/day of acetyl L-carnitine and 2-5 mg/kg body weight/day of propionyl L-carnitine or an equimolar amount of a pharmacologically acceptable salt thereof, in which the weight-ratio of acetyl L-carnitine to propionyl L-carnitine is 1:1.

7. A method for providing protection from a kidney dysfunction caused by lithium which comprises administering to an individual in need thereof a combination composition of 2-5 mg/kg body weight/day of acetyl L-carnitine and 2-5 mg/kg body weight/day of propionyl L-carnitine or an equimolar amount of a pharmacologically acceptable salt thereof, in which the weight-ratio of acetyl L-carnitine to propionyl L-carnitine is 1:1.

8. A method for providing protection from nephropathy caused by lithium which comprises administering to an individual in need thereof a combination composition of 2-5 mg/kg body weight/day of acetyl L-carnitine and 2-5 mg/kg body weight/day of propionyl L-carnitine or an equimolar amount of a pharmacologically acceptable salt thereof, in which the weight-ratio of acetyl L-carnitine to propionyl L-carnitine is 1:1.

9. A method for providing protection from tubular necrosis caused by lithium which comprises administering to an individual in need thereof a therapeutically effective amount of a combination composition of 2-5 mg/kg body weight/day of acetyl L-carnitine and 2-5 mg/kg body weight/day of propionyl L-carnitine or an equimolar amount of a pharmacologically acceptable salt thereof, in which the weight-ratio of acetyl L-carnitine to propionyl L-carnitine is 1:1.