IP Library Granted Patent US 12,414,934
Granted Patent B2
US 12,414,934 · App. 17/202,755 · Granted Sep 16, 2025

Combination therapies

Inventors: Daniel P. Gold (San Diego, CA); Miguel Quintela-Fandino (Madrid, ES)
Assignees: Aardvark Therapeutics, Inc.; The Spanish National Cancer Research Centre
A61K31/353A61K31/404A61K31/44A61K31/454A61K31/496A61K31/506A61K45/06C07K16/30A61K2300/00
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Quick Facts
Patent No.
US 12,414,934
App. No.
17/202,755
Granted
Sep 16, 2025
Kind
B2
Abstract

Provided herein are methods of treating and sensitizing cancer comprising administering a glycolytic inhibitor and an oxidative phosphorylation inhibitor.

Claims (17)

1. A method of treating a cancer that is prostate cancer, pancreatic cancer, leukemia, lymphoma, ovarian cancer, neuroblastoma, glioblastoma, kidney cancer, bladder cancer, gastrointestinal stromal tumors, liver cancer, head and neck cancer, lung cancer, melanoma, or a hematological malignancy, comprising administering to a subject in need thereof an effective amount of

(i) an angiogenesis inhibitor; and

(ii) 3-(4-hydroxyphenyl)-4-(4-hydroxyphenyl)-8-methylchroman-7-ol (compound 5).

2. The method of claim 1 , wherein the angiogenesis inhibitor is nintedanib, bevacizumab, sorafenib, sunitinib, thalidomide, dovitinib, regorafenib, or imatinib.

3. The method of claim 1 , wherein the angiogenesis inhibitor is nintedanib.

4. The method of claim 1 , wherein the angiogenesis inhibitor is bevacizumab.

5. The method of claim 1 , wherein the cancer is ovarian cancer, kidney cancer, liver cancer, or lung cancer.

6. The method of claim 1 , wherein the cancer is lung cancer.

7. The method of claim 1 , wherein the cancer is refractory, non-responsive, or resistant to chemotherapy and/or haploidentical stem cell transplantation.

8. The method of claim 7 , wherein the cancer is non-responsive or resistant to the angiogenesis inhibitor.

9. The method of claim 1 , wherein the angiogenesis inhibitor and 3-(4-hydroxyphenyl)-4-(4-hydroxyphenyl)-8-methylchroman-7-ol (compound 5) are administered simultaneously or sequentially.

10. A method of treating a chemoresistant cancer that is prostate cancer, pancreatic cancer, leukemia, lymphoma, ovarian cancer, neuroblastoma, glioblastoma, kidney cancer, bladder cancer, gastrointestinal stromal tumors, liver cancer, head and neck cancer, lung cancer, melanoma, or a hematological malignancy, comprising administering to a subject in need thereof an effective amount of

(i) an angiogenesis inhibitor; and

(ii) 3-(4-hydroxyphenyl)-4-(4-hydroxyphenyl)-8-methylchroman-7-ol (compound 5).

11. The method of claim 10 , wherein the chemoresistant cancer is ovarian cancer, kidney cancer, liver cancer, or lung cancer.

12. The method of claim 10 , wherein the chemoresistant cancer is resistant to the angiogenesis inhibitor.

13. The method of claim 10 , wherein the angiogenesis inhibitor is nintedanib.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 27, 2024
From: MEI PHARMA, INC
To: AARDVARK THERAPEUTICS, INC.
Reel/Frame 069422/0130 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 16, 2021
From: GOLD, DANIEL P.
To: MEI PHARMA, INC.
Reel/Frame 055605/0395 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 16, 2021
From: QUINTELA-FANDINO, MIGUEL
To: THE SPANISH NATIONAL CANCER RESEARCH CENTRE
Reel/Frame 055606/0214 →
Continuity (3)
Division 15546900
Provisional Application 62111030 · Feb 2, 2015
Related Publication 20210267936A1 · Sep 2, 2021
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Registration No. 4626-22-6, 4H-1-Benzopyran-4-one, 2,3-dihydro-7-hydroxy-3-(4-methoxyphenyl)-(9CI), Nov. 16, 1984. [cited by applicant]
Registration No. 67492-31-3, 4H-1-Benzopyran-4-one, 2,3-dihydro-7-hydroxy-3-(3-hydroxy-4-methoxyphenyl)-(9CI), Nov. 16, 1984. [cited by applicant]
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Registration No. 83206-83-1, 4H-1-Benzopyran-4-one, 3-(3,4-dimethoxyphenyl)-2,3-dihydro-7-hydroxy-(9CI), Nov. 16, 1984. [cited by applicant]
Registration No. 85915-64-6, 2H-1-Benzopyran-7-ol, 4-[5-(3,4-dihydro-7-hydroxy-2-H-1-benzopyran-3-yl)-4-hydroxy-2-methoxypheny1]-3,4-dihydro-3-(2-hydroxy-4-methoxypheny1)-,[3S-[3α-4β(R*)]]-(9CI), Nov. 16, 1984. [cited by applicant]
Registration No. 85915-66-8, 2H-1-Benzopyran, 4-[5-(3,4-dihydro-7-methoxy-2H-1-benzopyran-3-y1)-2,4-dimethoxypheny1]-3-(2,4-dimethoxypheny1)-3,4-dihydro-7-methoxy-, [3S-[3α4β(R*)]]-(9CI), Nov. 16, 1984. [cited by applicant]
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Registration No. 95457-39-9, 4H-1-Benzopyran-4-one-4-14C, 3-(3,4-dimethoxyphenyl)-7-hydroxy-(9CI), Mar. 23, 1985. [cited by applicant]
Registration No. 95541-42-7, 1,3-Benzenediol, 4-[3,4-dihydro-3-(2-hydroxy-4-methoxypheny1)-7-methoxy-2H-1-benzopyran-4-yl]-,(3R-trans)-(9CI), Mar. 30, 1985. [cited by applicant]
Registration No. 95541-43-8, 2H-Benzopyran, 3,4-bis(2,4-dimethoxyphenyl)-3,4-dihydro-7-methoxy-,(3R-trans)-(9CI), Mar. 30, 1985. [cited by applicant]
Registration No. 95541-44-9, 1,3,5-Benzenetrio1,2-[3,4-dihydro-3-(2-hydroxy-4-methoxypheny1)-7-methoxy-2H-1-benzopyran-4-yl)-,(3R-trans)-(9CI) (1984). [cited by applicant]
Registration No. 95541-45-0, 1,3,5-Benzenetrio1,2,4-bis[3,4-dihydro-3-(2-hydroxy-4-methoxypheny1)-7-methoxy-2H-1-benzopyran-4-yl]-,[3R-[3α,4β(3R*,4S″])-(9CI) (1984). [cited by applicant]
Registration No. 95541-46-1, 2H-1-Benzopyran,3-(2,4-dimethoxyphyeny1)-3,4-dihydro-7-methoxy-4(2,4,6-trimethoxyphenyl)-,(3R-trans)-(9CI) (1984). [cited by applicant]
Registration No. 95541-51-8, 2H-1-Benzopyran-7-ol,3-[3,4-dihydro-3-(2-hydroxy-4-methoxypheny1)-7-methoxy-2H-1-benzopyran-4-y1]-2-hydroxy-4-methoxypheny1]-3,4-dihydro-,[3R-3α,4β(S*)]-(9CI) (1984). [cited by applicant]
Registration No. 95541-53-0, 2H-1-Benzopyran,4-[5(3,4-dihyrdro-7-methoxy-2H-1-benzopyran-3-y1)-2,4-dimethoxypheny1]-3-(2,4-dimethoxypheny1)-3,4-dihydro-7-methoxy-,[3R-[3α,4β(S*)]]-(9CI) (1984). [cited by applicant]
Registration No. 95541-54-1, 2H-1-Benzopyran-7-ol,3-[-[4-dihydro-4-[4-hydroxy-5-(7-hydroxy-2H-1-benzopyran-3-y1)-2-methoxypheny1]-3-(2-hydroxy-4-methon/pheny1)-(3S-trans)-(9Cl) (1984). [cited by applicant]
Registration No. 95541-57-4, 2H-1-Benzopyran,4-[2,4-dimethoxy-5-(7-methoxy-2H-1-benzopyran-3-yl)phenyl]-3-(2,4-dimethoxyphenyl)-3,4-dihydro-7-methoxy-,(3S-trans)-(9CI) (1984). [cited by applicant]
Registration No. 95541-66-5, 2H-1-Benzopyran, 4-(2,4-dimethoxypheny1)-3,4-dihydro-7-methoxy-3-[4-methoxy-2-(methoxymethoxy)phenyl]-,(3R-trans)-(9Cl) (1984). [cited by applicant]
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