Methods and compositions for cancer treatment
US-2024424094-A1 · Dec 26, 2024 · US
US2016136197A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2016136197-A1 |
| Application number | US-201414898000-A |
| Country | US |
| Kind code | A1 |
| Filing date | Jun 13, 2014 |
| Priority date | Jun 14, 2013 |
| Publication date | May 19, 2016 |
| Grant date | — |
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The present invention relates to pharmaceutical compositions comprising an immunostimulatory amount of at least two immunopotentiators, wherein a first immunopotentiator is a non-methylated cytidyl guanosyl oligodeoxynucleotide (CpG ODN) and a second immunopotentiator is 3′,5′-cyclic diguanylic acid (c-di-GMP), and a pharmaceutically acceptable carrier. The invention also relates to the use of such pharmaceutical compositions for the induction of an immune response against tumor-specific antigens. Also the invention relates to their use in in situ tumor-destruction therapy and to such pharmaceutical compositions for use in the treatment of a mammal suffering from cancer.
Opening claim text (preview).
1 - 15 . (canceled) 16 . A pharmaceutical composition comprising an immunostimulating amount of at least two immunopotentiators and a pharmaceutically acceptable carrier; wherein a first immunopotentiator is a non-methylated cytidyl guanosyl oligodeoxynucleotide (CpG ODN); and wherein a second immunopotentiator is 3′,5′-cyclic diguanylic acid (c-di-GMP). 17 . A method of inducing an immune response against tumor-specific antigens in a mammal comprising administering the pharmaceutical composition of claim 16 to the mammal. 18 . A method of performing in situ tumor-destruction therapy in a mammal comprising performing tumor destruction on a tumor in the mammal and administering the pharmaceutical composition of claim 16 to the mammal. 19 . The method of claim 18 wherein the step of performing tumor destruction on the tumor is performed prior to the step of administering the pharmaceutical composition. 20 . The method of claim 19 wherein the step of administrating the pharmaceutical composition follows within 24 hours after the step of tumor destruction. 21 . The method of claim 20 wherein the step of administrating the pharmaceutical composition follows within 12 hours after the step of tumor destruction. 22 . The method of claim 20 wherein the step of administrating the pharmaceutical composition follows within 6 hours after the step of tumor destruction. 23 . A method of performing in situ tumor-destruction therapy in a mammal comprising performing tumor destruction on a tumor in the mammal and administering the pharmaceutical composition of claim 16 peri-operatively to the mammal. 24 . The method of claim 17 , wherein the mode of administering the pharmaceutical composition is intravenous, subcutaneous in the draining area of the neoplastic mass, peri-tumoral or intra-tumoral. 25 . A method of treating a mammal suffering from cancer comprising administering the pharmaceutical composition of claim 16 to the mammal. 26 . A method of treating a mammal suffering from cancer, comprising performing tumor destruction on a tumor in the mammal and administering the pharmaceutical composition of claim 16 peri-operatively to the mammal. 27 . The method of claim 26 wherein the step of performing tumor destruction on the tumor is performed prior to the step of administering the pharmaceutical composition. 28 . The method of claim 26 wherein the step of performing tumor destruction on the tumor is performed after the step of administering the pharmaceutical composition.
Antineoplastic agents · CPC title
Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00 · CPC title
Immunostimulants · CPC title
Compounds having three or more nucleosides or nucleotides · CPC title
Compounds having two nucleosides or nucleotides, e.g. nicotinamide-adenine dinucleotide, flavine-adenine dinucleotide · CPC title
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