Methods for treating pancreatic cancer using combination therapies comprising liposomal irinotecan
US-9492442-B2 · Nov 15, 2016 · US
US2016338956A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2016338956-A1 |
| Application number | US-201615227631-A |
| Country | US |
| Kind code | A1 |
| Filing date | Aug 3, 2016 |
| Priority date | May 3, 2004 |
| Publication date | Nov 24, 2016 |
| Grant date | — |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
The present invention provides liposome compositions containing substituted ammonium and/or polyanion, and optionally with a desired therapeutic or imaging entity. The present invention also provide methods of making the liposome compositions provided by the present invention.
Opening claim text (preview).
What is claimed is: 1 . A pharmaceutical composition comprising irinotecan sucrose octasulfate precipitated in a matrix comprising one or more phospholipids, wherein the matrix has a size of approximately 110 nm and comprises a total of 500-550 mg irinotecan base per mmol of total phospholipids. 2 . The liposome composition of claim 1 , wherein the matrix comprises DSPC and cholesterol. 3 . The liposome composition of claim 2 , wherein the matrix comprises DSPC, cholesterol, and PEG-DSPE in a molar ratio of 3:2:0.015. 4 . The liposome composition of claim 1 , wherein the matrix comprises a total of 500 mg irinotecan base per mmol of total DSPC and PEG-DSPE. 5 . The liposome composition of claim 4 , wherein the matrix comprises DSPC, cholesterol, and PEG-DSPE in a molar ratio of 3:2:0.015. 6 . The liposome composition of claim 1 , wherein the matrix comprises a PEGylated lipid. 7 . A pharmaceutical composition comprising irinotecan sucrose octasulfate within a matrix comprising one or more phospholipids and having a size of approximately 110 nm, wherein the composition comprises a total of 500-550 mg irinotecan base per mmol of total phospholipids in the matrix, wherein at least 90% of the irinotecan in the pharmaceutical composition is in the irinotecan sucrose octasulfate within the matrix. 8 . The liposome composition of claim 7 , wherein the matrix comprises a PEGylated lipid. 9 . The composition of claim 8 , wherein the irinotecan sucrose octasulfate is precipitated within the matrix from irinotecan hydrochloride and sucrose octasulfate triethylammonium. 10 . The composition of claim 9 , wherein the irinotecan sucrose octasulfate is precipitated within the matrix. 11 . The liposome composition of claim 10 , wherein the matrix comprises DSPC and cholesterol. 12 . The liposome composition of claim 11 , wherein the matrix comprises DSPC, cholesterol, and PEG-DSPE in a molar ratio of 3:2:0.015. 13 . The liposome composition of claim 11 , wherein the matrix comprises a total of 500 mg irinotecan base per mmol of total DSPC and PEG-DSPE. 14 . The liposome composition of claim 8 , wherein the PEGylated lipid is PEG-DSPE. 15 . The liposome composition of claim 7 , wherein the composition comprises a total of 500 mg irinotecan base per mmol of total DSPC and PEG-DSPE. 16 . A pharmaceutical composition comprising irinotecan sucrose octasulfate salt precipitated within a lipid matrix comprising DSPC, cholesterol, and PEG2000-DSPE and having a size of approximately 110-120 nm, wherein the composition comprises a total of 500 mg irinotecan base per mmol of total DSPC and PEG2000-DSPE in the matrix, and wherein at least 90% of the irinotecan in the pharmaceutical composition is in the irinotecan sucrose octasulfate within the matrix. 17 . The composition of claim 16 , wherein the matrix consists of DSPC, cholesterol, and PEG2000-DSPE in a molar ratio of 3:2:0.015. 18 . The composition of claim 16 , wherein the irinotecan sucrose octasulfate is precipitated as a salt in the matrix. 19 . The composition of claim 16 , wherein the irinotecan sucrose octasulfate is formed in the matrix from irinotecan hydrochloride and sucrose octasulfate triethylammonium. 20 . The composition of claim 17 , wherein the irinotecan sucrose octasulfate is precipitated within the matrix.
Antineoplastic agents · CPC title
Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00 · CPC title
Antibacterial agents · CPC title
Antivirals · CPC title
Synthetic bilayered vehicles, e.g. liposomes or liposomes with cholesterol as the only non-phosphatidyl surfactant · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.