Modified docetaxel liposome formulations and uses thereof
AssigneeMallinckrodt Inc.
InventorsWILLIAM McGHEE, JAMES BLACKLEDGE, MARGARET GRAPPERHAUS, LOUISE ROCHON, KRISHNA DEVARAKONDA
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AssigneeMallinckrodt Inc.
InventorsWILLIAM McGHEE, JAMES BLACKLEDGE, MARGARET GRAPPERHAUS, LOUISE ROCHON, KRISHNA DEVARAKONDA
Estimating the term…
The present invention provides compositions for the treatment of cancer. The compositions include liposomes containing a phosphatidylcholine lipid, a sterol, a PEG-lipid, and a taxane. The PEG-lipid constitutes from about 2 to about 8 mol % of the lipids in the liposome. The taxane is docetaxel esterified at the 2′-O position with a heterocyclyl-(C2-5 alkanoic acid). The present invention also provides liposomal compositions for the treatment of cancer comprising administering to a patient in need thereof a liposome, wherein the liposome comprises: a phosphatidylcholine lipid; a sterol; a PEG-lipid; and a taxane or a pharmaceutically acceptable salt thereof; wherein the taxane is docetaxel esterified at the 2′-O-position with a heterocyclyl-(C2-5alkanoic acid); and wherein upon administration of the liposomal composition to the patient, the plasma concentration of docetaxel remain above an efficacy threshold of 0.2 μM for at least 5 hours.
A pharmaceutical composition for the treatment of cancer comprising a liposomal formulation, wherein the liposomal formulation comprises:
A method of treating a cancer comprising administering to a patient in need thereof a pharmaceutical composition comprising a liposomal formulation, wherein the liposomal formulation comprises:
Dependencies are inferred from the claim text.