| CPC A61K 31/05 (2013.01) [A61K 9/0019 (2013.01); A61K 9/1075 (2013.01); A61K 31/282 (2013.01); A61K 31/4184 (2013.01); A61K 31/437 (2013.01); A61K 31/4523 (2013.01); A61K 31/506 (2013.01); A61K 31/519 (2013.01); A61K 31/655 (2013.01); A61K 31/704 (2013.01); A61K 35/17 (2013.01); A61K 39/0011 (2013.01); A61K 39/3955 (2013.01); A61K 47/06 (2013.01); A61K 47/10 (2013.01); A61K 47/26 (2013.01); A61K 47/44 (2013.01); A61P 35/00 (2018.01); A61K 2039/505 (2013.01); A61K 2039/545 (2013.01)] | 20 Claims |
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1. A method for inhibiting progression of lung cancer, colorectal cancer, or melanoma in a subject in need thereof, the method comprising administering to the subject a pharmaceutical composition that is a nanoemulsion comprising:
i) a single cannabinoid isolate that is a cannabidiol isolate, wherein the cannabidiol isolate is present at a concentration of at least 2% to about 12% w/v;
ii) at least 2% w/v olive oil;
iii) water;
iv) at least 0.05% w/v of polysorbate 80; and
v) terpenes consisting of about 0.25% w/v of each of limonene, myrcene, pinene, and linalool,
wherein the subject is being treated with chemotherapy or is recovering from chemotherapy, and the chemotherapy is a platinum-based agent or dacarbazine.
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