Gemcitabine prodrugs
AssigneeNuCana plc
InventorsHugh Griffith, Christopher McGuigan, Magdalena Slusarczyk, Michaela Serpi, Valentina Ferrari
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Abstract
This invention relates to a prodrug of the monophosphate nucleotide of the well-known oncology drug gemcitabine. Specifically, it relates to gemcitabine-[phenyl-benzoxy-L-alaninyl)]-phosphate when present as a single phosphate diastereoisomer and, in particular, it relates to the (S)-phosphate diastereoisomer which offers a remarkable and unexpected increase in solubility relative to the (R)-diastereoisomer. The (S)-phosphate epimer is also preferentially taken up into cyclodextrin solutions over the (R)-diastereoisomer.
Claims10
A method of treating cancer, comprising administering to a subject in need thereof a therapeutically effective amount of gemcitabine-[phenyl-(benzoxy-L-alaninyl)]-(S)-phosphate 3:
- or a pharmaceutically acceptable salt thereof, having a diastereoisomeric purity greater than 90%, wherein the cancer is selected from pancreatic cancer, ovarian cancer, lung cancer, bladder cancer, cholangiocarcinoma, renal cancer, cervical cancer, and thymic cancer.
Dependencies are inferred from the claim text.