IP Library Patent Application 13016135
Patent Application
App. No. 13/016,135

Method for Treating Liver Disorders with Receptor Associated Protein (RAP) Peptide-Fucosidase Inhibitor Conjugates

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Quick Facts
Patent No.
US None
App. No.
13/016,135
Abstract

The present invention relates, in general, to methods and compositions for the treatment of liver disorders and liver tumors, such as hepatocellular carcinoma, with a peptide of the receptor associated protein (RAP) molecule conjugated to a fucosidase inhibitor.

Claims (24)

1 . A peptide conjugate comprising a receptor associated protein (RAP) peptide linked to a fucosidase inhibitor, the RAP peptide comprising a polypeptide sequence at least 80% homologous to amino acids 210-319 of RAP of SEQ ID NO: 1.

2 . A peptide conjugate comprising a receptor associated protein (RAP) peptide linked to a fucosidase inhibitor, the RAP peptide comprising a polypeptide at least 80% homologous to the amino acid sequence set out in SEQ ID NO: 2.

3 . The peptide conjugate of claim 2 , wherein the RAP peptide comprises the amino acid sequence set out in SEQ ID NO: 2.

4 . The peptide conjugate of any one of claims 1 to 3 wherein the fucosidase inhibitor is selected from the group consisting of L-deoxyfuconojirimycin (DFJ), beta-1-C-methyl deoxymannojirimycin, beta-1-C-ethyl deoxymannojirimycin, beta-1-C-phenyl deoxymannojirimycin and (3R,4R,5S,6S)-1-butyl-4,5,6-trihydroxyazepane-3-carboxylic acid (Faz).

5 . The peptide conjugate of any one of claims 1 to 4 , wherein the fucosidase inhibitor is conjugated via a peptide linker.

6 . The peptide conjugate of claim 5 , wherein the peptide linker is a lysine dendrimer.

7 . The peptide conjugate of claim 6 , wherein the peptide linker is a K4K2K lysine dendrimer.

8 . The peptide conjugate of any one of claims 1 to 7 , wherein at least 4 fucosidase inhibitors are conjugated per RAP peptide molecule.

9 . The peptide conjugate of any one of claims 1 to 7 , wherein at least 8 fucosidase inhibitors are conjugated per RAP peptide molecule.

10 . A method for treating a liver tumor in a subject in need thereof comprising administering the peptide conjugate of any one of claims 1 to 9 in a therapeutically effective amount.

11 . The method of claim 10 , wherein the liver tumor is a result of hepatocellular carcinoma, hepatitis virus infection, cirrhosis, toxic liver damage, and hereditary hemochromatosis.

12 . The method of claim 11 , wherein the liver tumor is a result of hepatocellular carcinoma.

13 . The method of any one of claims 10 to 12 , wherein the treatment results in a decrease in liver tumor size in the subject.

14 . The method of any one of claims 10 to 13 , wherein the treatment results in a reduction of alpha-fetoprotein levels in blood of the subject compared to levels before treatment.

15 . The method of claim any one of claims 10 to 14 , wherein the peptide conjugate is administered intravenously.

16 . The method of claim 15 , wherein the peptide conjugate is administered via the hepatic artery.

17 . The method of any one of claims 10 to 14 , wherein the peptide conjugate is administered in combination with a second agent.

18 . The method of claim 17 , wherein the second agent is selected from the group consisting of a chemotherapeutic agent, a cytotoxic agent, a radioisotope, an anti-viral agent, an anti-fungal agent, an anti-inflammatory agent and an antibody.

19 . The method of claim 18 , wherein the chemotherapeutic agent is selected from the group consisting of doxorubicin and 5-fluorouracil.

20 . The method of claim 18 , wherein the second agent is a cytotoxic agent.

21 . The method of claim 20 , wherein the cytotoxic agent is selected from the group consisting of mechlorethamine hydrochloride, cyclophosphamide, ifosfamide, chlorambucil, melphalan, busulfan, thiotepa, carmustine, lomustine, dacarbazine and streptozocin.

22 . The method of claim 18 , wherein the second agent is a radioisotope.

23 . The method of claim 22 , wherein the radioisotope is selected from the group consisting of 131 I, 125 I, 111 In, 90 Y, 67 Cu, 127 Lu, 212 Bi, 213 Bi, 255 Fm, 149 Tb, 223 Rd, 213 Pb, 212 Pb, 211 At, 89 Sr, 153 Sm, 166 Ho, 225 Ac, 186 Re, 67 Ga, 68 Ga and 99m Tc.

24 . The method of claim 18 , wherein the liver tumor is associated with hepatitis virus infection, and the second agent is an antiviral agent.

Assignments (9)
RELEASE OF SECURITY INTEREST Recorded Oct 6, 2023
From: CITIBANK, N.A.
To: HORIZON THERAPEUTICS U.S. HOLDING LLC (FKA RAPTOR PHARMACEUTICALS INC.)
Reel/Frame 065178/0955 →
CHANGE OF NAME Recorded Dec 20, 2016
From: RAPTOR PHARMACEUTICALS INC.
To: HORIZON ORPHAN LLC
Reel/Frame 041034/0782 →
SECURITY AGREEMENT Recorded Oct 26, 2016
From: RAPTOR PHARMACEUTICALS INC.
To: CITIBANK, N.A., AS COLLATERAL AGENT
Reel/Frame 040479/0578 →
RELEASE OF SECURITY INTEREST Recorded Oct 25, 2016
From: HEALTHCARE ROYALTY GP II, LLC
To: RAPTOR PHARMACEUTICAL CORP.; RAPTOR DISCOVERIES INC.; RAPTOR PHARMACEUTICALS INC. (AS SUCCESSOR IN INTEREST TO RAPTOR THERAPEUTICS INC.)
Reel/Frame 040121/0801 →
MERGER Recorded Jan 28, 2013
From: RAPTOR DISCOVERIES INC.
To: RAPTOR PHARMACEUTICALS INC.
Reel/Frame 029701/0142 →
SECURITY AGREEMENT Recorded Dec 21, 2012
From: RAPTOR PHARMACEUTICAL CORP.; RAPTOR THERAPEUTICS INC.; RAPTOR DISCOVERIES INC.
To: HEALTHCARE ROYALTY PARTNERS II, L.P., AS LENDER
Reel/Frame 029531/0142 →
CHANGE OF NAME Recorded Jul 30, 2012
From: RAPTOR PHARMACEUTICAL INC.
To: RAPTOR DISCOVERIES INC.
Reel/Frame 028669/0320 →
CORRECTIVE ASSIGNMENT TO CORRECT THE NAME OF THE ASSIGNEE PREVIOUSLY RECORDED ON REEL 028187 FRAME 0104. ASSIGNOR(S) HEREBY CONFIRMS THE NAME OF THE ASSIGNEE SHOULD BE RAPTOR PHARMACEUTICAL INC.. Recorded Jul 27, 2012
From: ZANKEL, TODD C.
To: RAPTOR PHARMACEUTICAL INC.
Reel/Frame 028653/0797 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 10, 2012
From: ZANKEL, TODD C.
To: RAPTOR PHARMACEUTICALS INC.
Reel/Frame 028187/0104 →