US2003153620A1PendingUtilityA1
Treating eczema and/or psoriasis
Priority: May 12, 2000Filed: May 11, 2001Published: Aug 14, 2003
Est. expiryMay 12, 2020(expired)· nominal 20-yr term from priority
A61K 31/23A61P 17/04A61K 31/22
44
PatentIndex Score
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Claims
Abstract
The treatment of humans or other mammals for eczema and/or psoriasis using dosage forms or compositions that include cetyl myristate alone or (in admixture or serially) both cetyl myristate and cetyl palmitate.
Claims
exact text as granted — not AI-modified1 . A method of treatment and/or prophylaxis of a mammal for eczema and/or psoriasis which comprises or includes administering or having self administered to such mammal an effective amount of either
(a) cetyl myristate, or (b) cetyl myristate and cetyl palmitate.
2 . A method as claimed in claim 1 wherein said administration is orally of (b) whether as a mixture of both cetyl myristate and cetyl palmitate, or serially.
3 . A method of claim 1 or 2 where the effective amount is of (b).
4 . A method as claimed in claim 1 or 2 wherein said administration is with a mixture of cetyl myristate in conjunction with cetyl palmitate where the cetyl myristate comprises from 50 to 98% w/w of the mixture.
5 . A method of any one of the preceding claims wherein said effective amount of (a) or (b) is by means of one or more capsules.
6 . A method of any one of the preceding claims where said mammal is a human being suffering from eczema and the administration is for treatment purposes.
7 . A method of any one of claims 1 to 5 wherein said mammal is a human being suffering from psoriasis and the administration is for treatment purposes.
8 . A method of any one of the preceding claims where both cetyl myristate and cetyl palmitate in admixture are administered, the ratio by weight to weight being 95:5 respectively.
9 . A method of treatment of a human being for eczema which comprises or includes having administered to that human an effective amount of cetyl myristate.
10 . A method of treatment of a human being for psoriasis which comprises or includes having administered to that human an effective amount of cetyl myristate.
11 . An oral pharmaceutical composition for treating eczema which comprises or includes both cetyl myristate and cetyl palmitate.
12 . An oral pharmaceutical composition for treating psoriasis which comprises or includes both cetyl myristate and cetyl palmitate.
13 . A composition of claim 11 or claim 12 wherein said cetyl myristate comprises at least 50% by weight of the composition.
14 . A composition of any one of claims 11 to 13 which also includes at least one pharmaceutically acceptable excipient and/or diluent.
15 . An oral dosage unit effective in the treatment of eczema and/or psoriasis, said dosage unit having either
(a) cetyl myristate, or (b) a mixture of cetyl myristate and cetyl palmitate.
16 . A dosage unit as claimed in claim 15 wherein said dosage unit has (b) and said cetyl myristate in any such mixture comprises from 50 to 98% w/w of the mixture.
17 . A dosage unit as claimed in claim 15 wherein the dosage unit has (a) only and there is between 5 to 400 mg of cetyl myristate.
18 . A dosage unit of claim 16 wherein there is from 5 to 400 mg of the mixture of cetyl myristate and cetyl palmitate.
19 . A dosage unit of any one of claims 15 to 18 wherein (a) or (b) is in a capsule.
20 . A dosage unit as claimed in claim 18 wherein said capsule also includes a pharmaceutically acceptable excipient and/or diluent.
21 . A dosage unit of claim 20 which includes silicon dioxide.
22 . A dosage unit of any one of claims 15 to 21 which also contains calcium phosphate and/or magnesium oxide.
23 . A dosage unit of any one of claims 15 to 21 which also includes additionally at one trace element.
24 . A liquid composition being also a composition of any one of claims 12 to 14 or a dosage unit of any one of claims 15 to 18 .
25 . The use, in the manufacture of oral dosage units for the treatment or prophylaxis of eczema and/or psoriasis in a mammal, of
(a) cetyl myristate, or (b) a mixture of cetyl myristate and cetyl palmitate, or (c) cetyl palmitate.
26 . The use, in the manufacture of oral dosage units for the treatment or prophylaxis of eczema and/or psoriasis in a mammal, of
(i) cetyl myristate and (ii) cetyl palmitate.
27 . The use of claim 24 wherein (b) is used.
28 . The use of claim 26 or 27 wherein the ratio by weight of cetyl myristate to cetyl palmitate is 95:5.
29 . A method of any one of claims 1 to 10 substantially as hereinbefore described with reference to the examples.
30 . A dosage unit of any one of claims 15 to 23 substantially as hereinbefore described.
31 . A composition of any one of claims 11 to 14 and 24 substantially as hereinbefore described.
32 . The use of any one of claims 25 to 27 substantially as hereinbefore described.Join the waitlist — get patent alerts
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