The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Nov. 05, 2024

Filed:

Aug. 18, 2022
Applicants:

Provectus Pharmatech, Inc., Knoxville, TN (US);

Uti Limited Partnership, Calgary, CA;

Inventors:

Eric A. Wachter, Oak Ridge, TN (US);

Dominic Rodrigues, Knoxville, TN (US);

Satbir Thakur, Calgary, CA;

Lucy Swift, Calgary, CA;

Chunfen Zhang, Calgary, CA;

Mohit Jain, Calgary, CA;

Aru Narendran, Calgary, CA;

Assignees:

Provectus Pharmatech, Inc., Knoxville, TN (US);

UTI Limited Partnership, Calgary, CA;

Attorney:
Primary Examiner:
Int. Cl.
CPC ...
A61K 31/352 (2006.01); A61K 9/00 (2006.01); A61K 31/21 (2006.01); A61P 35/00 (2006.01); C07K 16/28 (2006.01);
U.S. Cl.
CPC ...
A61K 31/352 (2013.01); A61K 9/0019 (2013.01); A61K 31/21 (2013.01); A61P 35/00 (2018.01); C07K 16/2818 (2013.01); C07K 16/2827 (2013.01); C07K 16/2875 (2013.01);
Abstract

A method of treating a mammalian subject having hematologic, non-tumorous cancer cells is disclosed. The method comprises the steps of: (A) administering to such a mammalian subject a therapeutically effective amount of a halogenated xanthene, a pharmaceutically acceptable salt or a C-Calkyl ester thereof as a first cancer cytotoxic agent dissolved or dispersed in a pharmaceutically acceptable aqueous medium. The mammalian subject is maintained for a period of time sufficient to induce death of hematologic, non-tumorous cancer cells. A contemplated administration is typically repeated. A contemplated treatment method can also be carried out in conjunction with administration to said mammalian subject of a second therapeutically effective amount of a second, differently-acting cancer cytotoxic agent dissolved or dispersed in a pharmaceutically acceptable medium. The second cancer cytotoxic agent can be a small molecule or an intact antibody or paratope-containing portion thereof.


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