IP Library Patent Application 11795800
Patent Application
App. No. 11/795,800

Use of a Fatty Acid Composition Containing DHA for the Production of a Medical Product or a Food Stuff for the Treatment of Amyloidos-Related Diseases

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Patent No.
US None
App. No.
11/795,800
Abstract

A method for the treatment and/or prevention of amyloidos-related diseases, such as for example Alzheimer's disease and IgA nephropathy, comprising administering to a human or an animal a composition comprising at least (all-Z omega-3)-4,7,10,13,16,19-docosahexaenoic acid (DHA) is provided.

Claims (38)

1 - 36 . (canceled)

37 . A method for the treatment of amyloidos-related diseases, comprising administering to a human or an animal suffering from an amyloidos-related disease a fatty acid composition comprising (all-Z omega-3)-4,7,10,13,16,19-docosahexaenoic acid (DHA).

38 . A method according to claim 37 , wherein the fatty acid composition further comprises (all-Z omega-3)-5,8,11,14,17-eicosapentaenoic acid (EPA).

39 . A method according to claim 38 , wherein the weight ratio of EPA:DHA in the fatty acid composition is 1:X, where X is equal to or greater than 1.

40 . A method according to claim 38 , wherein the weight ratio of EPA:DHA in the fatty acid composition is from 1:1 to 1:8.

41 . A method according to claim 37 , wherein the fatty acids in the composition are presented in at least one of an esterified form, an ethyl ester form, a salt form, and a free acid form, or combination thereof.

42 . A method according to claim 37 , wherein at least DHA is obtained from at least one of a vegetable, a microbial, and an animal origin or a combination thereof.

43 . A method according to claim 38 , wherein at least one of DHA and EPA is obtained from at least one of a vegetable, a microbial, and an animal origin or a combination thereof.

44 . A method according to claim 38 , comprising EPA and/or DHA is obtained from a marine oil.

45 . A method according to claim 37 , wherein the fatty acid composition is obtained from a marine oil.

46 . A method according to claim 38 , wherein the fatty acid composition comprises EPA and DHA in a triglyceride form.

47 . A method according to claim 37 , wherein the fatty acid composition is administered orally to a human or an animal.

48 . A method according to claim 37 , wherein the fatty acid composition is administered in an amount providing a daily dosage of from 1 g to 15 g of said fatty acid composition.

49 . A method according to claim 37 , wherein the amyloidos-related disease is Alzheimer's disease.

50 . A method according to claim 37 , wherein the amyloidos-related disease is IgA nephropathy.

51 . A method according to claim 37 , wherein the amyloidos-related disease is type II diabetes mellitus.

52 . A method according to claim 37 , wherein the amyloidos-related disease is chosen from Parkinson's disease, kidney amyloidoses secondary to chronic inflammatory disease, or Creutzfeld-Jacob disease.

53 . A method according to claim 37 , wherein the administration to a human will prevent the formation of aggregates of protein fibrils or plaque and/or reduce deposed fibrils.

54 . A method for treatment of Alzheimer's disease, comprising administering to a human or an animal suffering from Alzheimer's disease a fatty acid composition comprising (all-Z omega-3)-5,8,11,14,17-eicosapentaenoic acid (EPA) and (all-Z omega-3)-4,7,10,13,16,19-docosahexaenoic acid (DHA).

55 . A method according to claim 54 , wherein the EPA and DHA are present in the composition in an EPA:DHA ratio from 1:2 to 2:1.55.

56 . A method according to claim 54 , wherein the weight ratio of EPA:DHA in the fatty acid composition is 1:X, where X is equal to or greater than 1.

57 . A method according to claim 56 , wherein the weight ratio of EPA:DHA in the fatty acid composition is from 1:1 to 1:8.

58 . A method according to claim 54 , wherein the fatty acids in the composition are present in at least one of an esterified form, an ethyl ester form, a salt form, and a free acid form, or combinations thereof.

59 . A method according to claim 54 , wherein at least one of DHA and EPA is obtained from at least one of a vegetable, a microbial, and an animal origins or a combinations thereof.

60 . A method according to claim 54 , comprising EPA and/or DHA is obtained from a marine oil.

61 . A method according to claim 54 , wherein the fatty acid composition is obtained from a marine oil.

62 . A method according to claim 54 , wherein the fatty acid composition comprises EPA and DHA in a triglyceride form.

63 . A method according to claim 54 , wherein the fatty acid composition is administered orally to a human or an animal.

64 . A method according to claim 54 , wherein the fatty acid composition is administered in an amount providing a daily dosage of from 1 g to 15 g of said fatty acid composition.

65 . A method according to claim 54 , wherein the administration to a human will prevent misfolding of protein fibrils or plaque and/or reduce deposed fibrils or plaque.

66 . A method for treatment of amyloidoses, comprising administering to a human or an animal suffering from amyloidoses a fatty acid composition comprising (all-Z omega-3)-4,7,10,13,16,19-docosahexaenoic acid (DHA).

67 . A method according to claim 66 , wherein the fatty acid composition further comprises (all-Z omega-3)-5,8,11,14,17-eicosapentaenoic acid (EPA).

68 . A method according to claim 66 , wherein the weight ratio of EPA:DHA in the fatty acid composition is 1:X, where X is equal to or greater than 1.

69 . A method according to claim 38 , wherein the weight ratio of EPA:DHA in the fatty acid composition is from 1:1 to 1:6.

70 . A method according to claim 44 , wherein the marine oil is a fish oil.

71 . A method according to claim 48 , wherein said fatty acid composition is administered in an amount providing a daily dosage of from 2 g to 6 g of said fatty acid composition.

72 . A method according to claim 57 , wherein the weight ratio of EPA:DHA in the fatty acid composition is from 1:1 to 1:6.

73 . A method according to claim 64 , wherein the fatty acid composition is administered in an amount providing a daily dosage of from 2 g to 6 g of said fatty acid composition.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 13, 2008
From: BRYHN, MORTEN; SLETTEN, KNUT; WESTERMARK, GUNILLA TORSTENSDOTTER; WESTERMARK, PER OLOF
To: PRONOVA BIOCARE AS
Reel/Frame 020967/0026 →
CHANGE OF NAME Recorded Sep 10, 2007
From: PRONOVA BIOCARE A/S
To: PRONOVA BIOPHARMA NORGE AS
Reel/Frame 019795/0594 →