US2013164330A1PendingUtilityA1
Methods and Compositions for Treatment of Hematologic Cancers
Est. expiryAug 20, 2024(expired)· nominal 20-yr term from priority
C12N 2770/32332C12N 2770/32032A61K 39/125A61K 35/768A61P 35/00A61K 45/06A61P 35/02C12N 2770/32321A61P 35/04C12N 7/00Y02A50/30
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Claims
Abstract
The present invention relates to oncolytic Picornaviruses and methods and compositions for treating subjects having hematologic cancers. These include methods and compositions for treatment of myeloma, using disclosed Picornavirus such as Coxsackievirus, in methods of direct or indirect administration to subjects and ex vivo purging of malignant cells within auto grafts prior to transplantation.
Claims
exact text as granted — not AI-modified1 . A method for treating and/or preventing hematologic cancer in a subject, the method comprising administering a therapeutically effective amount of an intercellular adhesion molecule-1 (CAM-1) binding Picornavirus or a modified form thereof such that at least some cells of the cancer undergo viral oncolysis.
2 . The method according to claim 1 , wherein the Picornavirus is selected from the group consisting of prototype and clinically isolated strains of enteroviruses.
3 - 22 . (canceled)
23 . The method according to claim 2 , wherein the enterovirus is selected from the group consisting of Coxsackievirus, Echovirus, Poliovirus, unclassified enteroviruses, Rhinovirus, Paraechovirus, Hepatovirus, and Cardiovirus.
24 . The method according to claim 1 , wherein the Picornavirus is a Coxsackie A group virus selected from the group consisting of CVA13, CVA15, CVA18, CVA20, CVA21, modified forms thereof, and combinations thereof.
25 . The method according to claim 1 , wherein the Picornavirus is administered intravenously, intratumorally, intraperitoneally, intramuscularly, ex vivo purging of malignant cells within auto grafts prior to autologous stem cell transplantation, or by ex vivo purging of malignant cells within auto grafts prior to transplantation.
26 . The method according to claim 25 , wherein the auto grafts comprise hematopoietic stem cells.
27 . The method according to claim 1 , wherein the range of viral dose is between about 0.01 to about 1000 infectious viral units per cell.
28 . The method according to claim 1 , wherein the virus is administered to a subject in combination with an effective amount of a chemotherapeutic agent.
29 . The method according to claim 1 , wherein the virus is administered to a subject in combination with an effective amount of a probiotic agent.
30 . The method according to claim 1 , wherein the hematologic cancer is a cancer selected from the group consisting of multiple myeloma, leukemia, lymphoma, Hodgkin's disease, non-Hodgkin's disease and myelodysplasia.
31 . The method according to claim 1 , wherein the hematologic cancer is B cell lymphoma.
32 . The method according to claim 1 , wherein the hematologic cancer is a leukemia selected from the group consisting of chronic myelogenous leukemia, acute lymphocytic leukemia (ALL), chronic lymphocytic leukemia (CLL), B prolymphocytic leukemia and monocytic leukemia.
33 . The method according to claim 1 , wherein cells of the hematologic cancer over-express the virus-cell entry receptor molecules intercellular adhesion molecule-1 (ICAM-1) and/or decay-accelerating factor (DAF).
34 . The method according to claim 1 , wherein the subject is a human.
35 . A method for treating and/or preventing hematologic cancer in a subject, the method comprising administering a therapeutically effective amount of a nucleic acid molecule derived from an ICAM-1 binding Picornavirus or a modified form thereof such that at least some cells of the cancer are killed by the virus.
36 . The method according to claim 35 , wherein the Picornavirus is a Coxsackie A group virus selected from the group consisting of CVA13, CVA15, CVA18, CVA20, CVA21.
37 . The method according to claim 35 , wherein the subject is a human.
38 . A method for inducing an immune response in a subject against hematologic tumor or cancer cells, the method comprising infecting said cells of the subject with a therapeutically effective amount of an ICAM-1 binding Picornavirus or a modified form thereof such that at least some cells of the cancer undergo viral oncolysis.Join the waitlist — get patent alerts
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