IP Library Granted Patent US 8,057,787
Granted Patent B2
US 8,057,787 · App. 12/082,389 · Granted Nov 15, 2011

Protease resistant modified interferon-beta polypeptides

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Quick Facts
Patent No.
US 8,057,787
App. No.
12/082,389
Granted
Nov 15, 2011
Kind
B2
Abstract

Protease resistant modified interferon-beta polypeptides, pharmaceutical compositions and methods of treatment administering the compositions are provided. The modified interferon-beta polypeptides are orally available; hence pharmaceutical compositions formulated for oral administration also are provided.

Claims (19)

1. A modified interferon beta (IFN beta) cytokine, wherein said modified IFN beta cytokine differs from an unmodified IFN beta cytokine by two amino acid substitutions,

wherein said unmodified IFN beta cytokine comprises the amino acid sequence of SEQ ID NO: 196,

said two amino acid substitutions being either:

(a) substitution of the 5th and 47th positions in SEQ ID NO: 196, with aspartic acid and isoleucine, respectively; or

(b) substitution of the 5th and 47th positions in SEQ ID NO: 196, with asparagine and isoleucine, respectively; or

(c) substitution of the 6th and 47th positions in SEQ ID NO: 196, with glutamine and isoleucine, respectively,

and wherein said two amino acid substitutions confer increased resistance to proteolysis over the unmodified IFN beta cytokine.

2. The modified IFN beta cytokine of claim 1 , wherein only the primary amino acid sequence of said unmodified IFN beta cytokine is modified.

3. A pharmaceutical composition comprising the modified IFN beta cytokine of claim 1 .

4. The pharmaceutical composition of claim 3 , further comprising a pharmaceutically acceptable carrier or excipient.

5. The pharmaceutical composition of claim 4 , wherein the pharmaceutically acceptable carrier or excipient is selected from the group consisting of a binding agent, a filler, a lubricant, a disintegrant, and a wetting agent.

6. The pharmaceutical composition of claim 3 , further comprising a pharmaceutically acceptable additive.

7. The pharmaceutical composition of claim 6 , wherein the pharmaceutically acceptable additive is selected from the group consisting of a suspending agent, an emulsifying agent, a non-aqueous vehicle, and a preservative.

8. The pharmaceutical composition of claim 3 , wherein the composition is in the form of a liquid, a solution, a suspension, an aerosol, a tablet, a lozenge or a capsule.

9. The pharmaceutical composition of claim 8 , wherein the composition is in the form of a tablet or a capsule.

10. The pharmaceutical composition of claim 3 , wherein said composition is formulated for oral, parenteral, intravenous, intradermal, subcutaneous, buccal, inhalation, intramuscular, rectal or topical administration.

11. The pharmaceutical composition of claim 10 , wherein said composition is formulated for oral administration.

12. The pharmaceutical composition of claim 11 , wherein the pharmaceutical composition is formulated for oral administration to the mouth or gastrointestinal tract.

13. The pharmaceutical composition of claim 3 , wherein the pharmaceutical composition is formulated for controlled-release of the modified IFN beta cytokine.

Assignments (4)
CHANGE OF NAME Recorded May 17, 2010
From: HANALL PHARMACEUTICAL CO., LTD.
To: HANALL BIOPHARMA CO., LTD.
Reel/Frame 024393/0954 →
CORRECTIVE ASSIGNMENT TO CORRECT THE ASSIGNEE'S COUNTRY PREVIOUSLY RECORDED ON REEL 023045 FRAME 0184. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNEE'S COUNTRY IS: THE REPUBLIC OF KOREA (SOUTH KOREA). Recorded Nov 4, 2009
From: NAUTILUS BIOTECH S.A.
To: HANALL PHARMACEUTICAL CO., LTD.
Reel/Frame 023470/0613 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 3, 2009
From: NAUTILUS BIOTECH S.A.
To: HANALL PHARMACEUTICAL CO., LTD.
Reel/Frame 023045/0184 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 5, 2008
From: GANTIER, RENE; VEGA, MANUEL; DRITTANTI, LILA; GUYON, THIERRY
To: NAUTILUS BIOTECH, S.A.
Reel/Frame 020901/0586 →