IP Library Patent Application 13090983
Patent Application
App. No. 13/090,983

Treatment of Non-Neuronal Cancer using HSV-1 Variants

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Quick Facts
Patent No.
US None
App. No.
13/090,983
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 (10)

1 . A method of treating a malignant mesothelioma in a human, said method comprising administering to a human having a malignant mesothelioma an effective amount of a mutant herpes simplex virus type 1 (HSV-1), said HSV-1 having an HSV-1 genome having a modification in respect of the wild-type genome which consists of mutation in the γ34.5 genes such that the γ34.5 genes are non-functional, wherein the HSV-1 infects, replicates within, and lyses malignant mesothelioma cells in said human, thereby treating the malignant mesothelioma, and wherein said HSV-1 infection, replication and lysis is restricted to the malignant mesothelioma cells.

2 . The method according to claim 1 wherein the malignant mesothelioma is in the peritoneum.

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

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

5 . 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 (RL) of the viral genome.

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 (RL) of the viral genome, wherein the modification is a deletion from 0.1 to 3 Kb.

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 (RL) of the viral genome, wherein the modification is a deletion of from 0.7 to 0.9 Kb.

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

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

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

Assignments (5)
CHANGE OF NAME Recorded Oct 11, 2012
From: CRUSADE LABORATORIES LIMITED
To: VIRTTU BIOLOGICS LIMITED
Reel/Frame 029111/0390 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 29, 2011
From: BROWN, SUSANNE MOIRA; MACLEAN, ALASDAIR RODERICK
To: THE UNIVERSITY COURT OF THE UNIVERSITY OF GLASGOW
Reel/Frame 026675/0774 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 29, 2011
From: THE UNIVERSITY COURT OF THE UNIVERSITY OF GLASGOW
To: CRUSADE LABORATORIES LIMITED
Reel/Frame 026675/0788 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 29, 2011
From: RANDAZZO, BRUCE P.; ALBELDA, STEVEN; KAISER, LARRY; KUCHARCZUK, JOHN
To: THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA
Reel/Frame 026675/0810 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 29, 2011
From: FRASER, NIGEL W.
To: WISTAR INSTITUTE
Reel/Frame 026675/0841 →