IP Library Patent Application 11765189
Patent Application
App. No. 11/765,189

TREATMENT OF NON-NEURONAL CANCER USING HSV-1 VARIANTS

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Quick Facts
Patent No.
US None
App. No.
11/765,189
Abstract

A mutant herpes simplex virus which has been modified in the γ34.5 gene such that the gene is non-functional is used to treat a non-neuronal cancer such as a mesothelioma, ovarian carcinoma, bladder cancer or melanoma. Typically, the mutant herpes simplex virus has been modified within the BamHI restriction fragment of the long terminal repeat of the viral genome.

Claims (12)

1 . A method of treating a non-neuronal cancer which does not occur in the central nervous system, and comprises a non-neuronal tumor cell, in a mammal, wherein the cancer is a mesothelioma, said method comprising the step of administering to the mammal an effective amount of a mutant herpes simplex virus type 1 (HSV-1) said HSV-1 consisting of an HSV-1 genome which is modified in respect of the wild-type by modification to the HSV-1 genome wherein said modification consists of mutation in the γ34.5 gene so as to become a non-functional γ34.5 gene, wherein the HSV-1 infects, replicates within, and lyses said non-neuronal tumor cell in said mammal, thereby treating the non-neuronal cancer.

2 . The method according to claim 1 wherein the mammal is a human.

3 . The method according to claim 1 wherein the cancer is a primary tumor.

4 . The method according to claim 1 wherein the cancer is a metastatic tumor.

5 . (canceled)

6 . The method according to claim 1 wherein the mutant herpes simplex virus is modified within the Bam HI s restriction fragment of the long repeat region (R L ) of the viral genome.

7 . The method according to claim 1 wherein the mutant herpes simplex virus is modified within the Bam HI s restriction fragment of the long repeat region (R L ) of the viral genome, wherein the modification is a deletion of from 0.1 to 3 Kb.

8 . The method according to claim 1 wherein the mutant herpes simplex virus is modified within the Bam HI s restriction fragment of the long repeat region (R L ) of the viral genome, wherein the modification is a deletion of from 0.7 to 0.8 Kb.

9 . The method according to claim 1 wherein the modification is a 759 bp deletion in the γ34.5 gene.

10 . The method according to claim 1 wherein the mutant herpes simplex virus is a mutant of strain 17.

11 . The method according to claim 1 wherein the mutant herpes simplex virus is HSV1716.

12 .- 13 . (canceled)

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 3, 2007
From: THE UNIVERSITY COURT OF THE UNIVERSITY OF GLASGOW
To: CRUSADE LABORATORIES LIMITED
Reel/Frame 019512/0670 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 2, 2007
From: KUCHARCZUK, JOHN; RANDAZZO, BRUCE; ALBELDA, STEVEN; KAISER, LARRY
To: THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA
Reel/Frame 019508/0570 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 2, 2007
From: BROWN, SUSANNE MOIRA; MACLEAN, ALASDAIR RODERICK
To: THE UNIVERSITY COURT OF THE UNIVERSITY OF GLASGOW
Reel/Frame 019508/0619 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 2, 2007
From: FRASER, NIGEL WILLIAM
To: THE WISTAR INSTITUTE
Reel/Frame 019508/0626 →