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US 12,240,870 B2Granted
Sequencing method for CAR T cell therapy
AssigneesPurdue Research Foundation, Endocyte, Inc., Seattle Children's Hospital
InventorsRichard Messmann, Christopher Paul Leamon, Haiyan Chu, Yingjuan June Lu, Philip Stewart Low, Michael C. Jensen, James Matthaei, Navin Robert Charles Pinto, Julie Ruggieri Park
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Abstract
The present disclosure relates to methods of treating a patient with a cancer by administering to the patient a composition comprising CAR T cells and administering to the patient a small molecule linked to a targeting moiety by a linker. The disclosure also relates to compositions for use in such methods.
Claims14
A method of treating a patient for cancer, the method comprising
- i) administering to the patient at least one dose of a chimeric antigen receptor T cell (CAR T cell) composition comprising CAR T cells comprising a chimeric antigen receptor (CAR) directed to a targeting moiety;
- and
- ii) administering to the patient a compound, or a pharmaceutically acceptable salt thereof, wherein the compound comprises a small molecule ligand linked to the targeting moiety by a linker, wherein the small molecule ligand is folate and wherein the targeting moiety is fluorescein, or a pharmaceutically acceptable salt thereof, fluorescein isothiocyanate (FITC), or NHS-fluorescein, and wherein the compound, or the pharmaceutically acceptable salt thereof, is administered in at least a first dose escalation sequence and a second dose escalation sequence, wherein a full dose of the compound, or the pharmaceutically acceptable salt thereof, is 10 μg/kg to 50 μg/kg of the compound, or the pharmaceutically acceptable salt thereof;
- wherein the first dose escalation sequence for the compound, or the pharmaceutically acceptable salt thereof, comprises administering 3 separate escalating doses up to the full dose of the compound on three separate days in a first two-week cycle;
- and
- wherein the second dose escalation sequence for the compound, or the pharmaceutically acceptable salt thereof, comprises administering 3 separate escalating doses up to the full dose of the compound on three separate days in a second two-week cycle,
- whereupon the patient is treated for cancer, and wherein the patient is a human.
4 more elements
Dependencies are inferred from the claim text.