US2006229234A1PendingUtilityA1
Peptide factor
Individually held — no corporate assignee on recordPriority: Mar 28, 1998Filed: Jun 14, 2006Published: Oct 12, 2006
Est. expiryMar 28, 2018(expired)· nominal 20-yr term from priority
A61P 7/00A61P 43/00A61P 37/06A61P 9/14A61P 31/00A61P 29/00A61P 11/00A61P 17/00A61P 1/00A61P 19/04A61P 19/02C12N 15/67C07K 14/57581C12N 15/79A61K 38/00A61K 38/22Y02A50/30
52
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Claims
Abstract
The present invention relates to use of oxidised thymosin β 4 in therapy, more particularly in the treatment of diseases or conditions associated with an inflammatory response or septic shock. The present invention also provides pharmaceutical formulations comprising oxidised thymosin β 4 together with a suitable excipient.
Claims
exact text as granted — not AI-modified1 . A pharmaceutical formulation comprising as an active agent isolated oxidised thymosin β4, a variant having the physiological activity of oxidized thymosin β4 or salt thereof and a pharmaceutically acceptable carrier therefor.
2 . The pharmaceutical formulation claim 1 wherein the oxidised thymosin β4 is a form of thymosin β4 in which a methionine residue 6 amino acids from the N-terminus is oxidised to methionine sulphoxide.
3 . The pharmaceutical formulation of claim 1 wherein the oxidised thymosin β4 is a form of thymosin in which the sulphur of a methionine residue 6 amino acids from the N-terminus is complexed with a metal(s).
4 . The pharmaceutical formulation of claim 1 wherein the physiologically active variant is an oxidised peptide which is a truncated form of oxidised thymosin β4.
5 . The pharmaceutical formulation of claim 1 wherein the oxidised thymosin β4 is of mammalian origin.
6 . The pharmaceutical formulation of claim 1 wherein the oxidised thymosin β4 is synthetic.
7 . The pharmaceutical formulation of claim 1 wherein the oxidised thymosin β4, variant, or salt thereof accounts for at least 30% of any thymosin β4 present in the formulation.
8 . The pharmaceutical formulation of claim 1 wherein the oxidised thymosin β4, variant, or salt thereof comprises substantially no non-oxidised thymosin β4.
9 . The pharmaceutical formulation of claim 8 comprising a further pharmaceutical agent, wherein a side effect of the further pharmaceutical agent is inflammation.
10 . The pharmaceutical formulation of claim 7 suitable for oral, nasal, topical, rectal, vaginal or parenteral administration or for inhalation.
11 . The pharmaceutical formulation of claim 2 wherein the oxidized methionine is further oxidized to methionine sulphone.
12 . A compound which is an isolated oxidized form of synthetic or expressed thymosin β4 or a variant having oxidized thymosin β4 activity, or a pharmaceutically acceptable salt thereof.
13 . The compound of claim 12 , further comprising a pharmaceutically acceptable carrier.
14 . The compound of claim 12 , which is a variant of oxidized thymosin β4 that is a truncated or a deleted form thereof.
15 . The compound of claim 12 , wherein said variant differs from oxidized thymosin β4 in that an amino acid is replaced by a conservative amino acid residue.Join the waitlist — get patent alerts
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