US2007207149A1PendingUtilityA1
Cancer treatment using viruses and camptothecins
Est. expiryApr 27, 2024(expired)· nominal 20-yr term from priority
A61P 35/00A61K 39/39558C12N 2760/18132A61K 35/768A61K 31/4745A61K 45/06A61P 43/00A61K 39/12Y02A50/30
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Claims
Abstract
Mammalian subjects having a neoplasm are treated with a virus and a camptothecin compound, for example irinotecan or topotecan. The virus is selected from the group consisting of a Newcastle disease virus, a measles virus, a vesicular stomatitis virus, an influenza virus, a Sindbis virus, a picornavirus, and a myxoma virus. The treatment can also include administration of a monoclonal antibody against epidermal growth factor receptor, for example cetuximab.
Claims
exact text as granted — not AI-modified1 . A method of treating a mammalian subject having a neoplasm, comprising
administering to the subject a virus and a camptothecin compound in a combined amount effective to treat the subject; wherein the virus is selected from the group consisting of a Newcastle disease virus, a measles virus, a vesicular stomatitis virus, an influenza virus, a Sindbis virus, a picornavirus, and a myxoma virus.
2 . The method of claim 1 , further comprising administering to the subject a monoclonal antibody against epidermal growth factor receptor in an amount effective, in combination with the virus and the camptothecin compound, to treat the subject.
3 - 5 . (canceled)
6 . The method of claim 1 , wherein the virus is replication-competent.
7 . The method of claim 1 , wherein the virus is a Newcastle Disease virus.
8 . The method of claim 7 , wherein the virus is a mesogenic strain of Newcastle Disease virus.
9 . The method of claim 1 , wherein the virus is a picornavirus selected from the group consisting of a poliovirus, an echovirus, and a coxsackievirus.
10 . The method of claim 9 , wherein the virus is a coxsackievirus selected from type A21, A13, A15 and A18.
11 . The method of claim 9 , wherein the virus is an echovirus type 1.
12 . The method of claim 1 , wherein the virus is administered intravenously.
13 . The method of claim 1 wherein the camptothecin compound is selected from the group consisting of irinotecan, topotecan, 9-aminocamptothecin, exatecan, karenitecin, rubitecan, lurtotecan, and a homocamptothecin.
14 . The method of claim 13 , wherein the camptothecin compound is irinotecan.
15 . The method of claim 1 , wherein the camptothecin compound and the virus are administered to the subject within a single twenty-four hour period.
16 . The method of claim 1 , wherein the camptothecin compound is administered from twenty-four hours to one month before administration of the virus.
17 . The method of claim 16 , wherein the camptothecin compound is administered from twenty-four hours to one week before administration of the virus.
18 . The method of claim 1 , wherein the camptothecin compound is administered to the subject from twenty-four hours to one month after administration of the virus.
19 . The method of claim 18 , wherein the camptothecin compound is administered to the subject from twenty-four hours to one week after administration of the virus.
20 . The method of claim 2 , wherein the monoclonal antibody is cetuximab.Cited by (0)
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