CPC A61K 39/0011 (2013.01) [A61K 9/0019 (2013.01); A61K 35/12 (2013.01); A61K 35/17 (2013.01); A61K 39/39558 (2013.01); A61K 47/551 (2017.08); A61K 47/555 (2017.08); A61K 48/005 (2013.01); A61P 35/00 (2018.01); C07K 14/7051 (2013.01); C07K 14/70517 (2013.01); C07K 16/44 (2013.01); C12N 15/86 (2013.01); A61K 2039/505 (2013.01); A61K 2039/5156 (2013.01); C07K 2317/622 (2013.01); C07K 2317/73 (2013.01); C07K 2317/92 (2013.01); C07K 2319/02 (2013.01); C07K 2319/03 (2013.01); C07K 2319/33 (2013.01); C12N 2740/15043 (2013.01); C12N 2740/16043 (2013.01)] | 14 Claims |
1. A method of treating a patient for cancer, the method comprising:
administering to the patient a chimeric antigen receptor T cell (CAR T cell) composition, wherein the CAR T cell comprises a chimeric antigen receptor (CAR) directed to fluorescein isothiocyanate (FITC), and
administering to the patient an effective amount of a first conjugate, or a pharmaceutically acceptable salt thereof, wherein the first conjugate comprises an NK-1 receptor-binding ligand (NK1RL) and FITC,
wherein the NK1RL is a small molecule comprising
![]() wherein the CAR T cell comprises a nucleic acid comprising SEQ ID NO: 1 or SEQ ID NO: 3,
wherein the cancer is an NK-1 receptor-expressing cancer, and
wherein the patient is treated for cancer.
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