Biomarkers predictive of cancer cell response to ML329 or a derivative thereof

US12560609B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-12560609-B2
Application numberUS-201917294475-A
CountryUS
Kind codeB2
Filing dateNov 25, 2019
Priority dateNov 26, 2018
Publication dateFeb 24, 2026
Grant dateFeb 24, 2026

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

The present invention is based in part on the identification of biomarkers, including NQO1, NRF2 and KEAP1, predictive of cancer cell responsiveness to treatment with ML 329 or a derivative thereof.

First claim

Opening claim text (preview).

What is claimed is: 1 . A method of treating a cancer in a subject likely to be responsive to 4-[(1,4-dioxo-1,4-dihydronapthalen-2-yl)amino]benzenesulfonamide (ML329) or an ML329 derivative selected from: the method comprising: i) selecting the subject likely to be responsive to ML329 or the ML329 derivative, the subject having been identified by determining the presence of a KEAP1 loss-of-function mutation in cancer cells from the subject wherein the presence of the kelch-like ECH-associated protein 1 (KEAP1) loss-of-function mutation identifies the subject as likely to be responsive to ML329 or the ML329 derivative; and ii) administering ML329 or the ML329 derivative to the selected subject. 2 . The method of claim 1 , wherein the subject's cancer cells have KEAP1 loss-of-function. 3 . The method of claim 1 , wherein the KEAP1 loss-of-function mutation is a coding region mutation. 4 . The method of claim 1 , wherein the cancer is selected from the group consisting of melanoma, lung cancer, head and neck squamous cell carcinomas, kidney cancer, pancreas cancer, prostate cancer, bladder cancer, uterine cancer, head and neck cancer, and esophagus cancer. 5 . The method of claim 1 , wherein the subject is likely to be responsive to ML329 and the method comprises administering ML329 to the selected subject. 6 . The method of claim 1 , wherein the subject is likely to be responsive to the ML329 derivative, SCAP105461, and the method comprises administering SCAP105461 to the selected subject. 7 . The method of claim 1 , wherein the subject is likely to be responsive to the ML329 derivative, SCAP105463, and the method comprises administering SCAP105463 to the selected subject. 8 . The method of claim 1 , wherein the subject is a) an animal model of cancer; b) a mammal; c) a mouse; or d) a human. 9 . The method of claim 1 , wherein the cancer is a lung cancer. 10 . The method of claim 5 , wherein the cancer is a lung cancer. 11 . The method of claim 6 , wherein the cancer is a lung cancer. 12 . The method of claim 7 , wherein the cancer is a lung cancer.

Assignees

Inventors

Classifications

  • acting on NADH or NADPH (1.6), e.g. those with a heme protein as acceptor (1.6.2) (general), Cytochrome-b5 reductase (1.6.2.2) or NADPH-cytochrome P450 reductase (1.6.2.4) · CPC title

  • Nucleoproteins · CPC title

  • Sulfonamides (compounds containing a para-N-benzene-sulfonyl-N- group A61K31/63) · CPC title

  • G01N33/575Primary

    for cancer · CPC title

  • for testing toxicity · CPC title

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Frequently asked questions

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What does patent US12560609B2 cover?
The present invention is based in part on the identification of biomarkers, including NQO1, NRF2 and KEAP1, predictive of cancer cell responsiveness to treatment with ML 329 or a derivative thereof.
Who is the assignee on this patent?
Dana Farber Cancer Inst Inc, Massachusetts Gen Hospital, Univ Kansas
What technology area does this patent fall under?
Primary CPC classification G01N33/575. Mapped technology areas include Physics.
When was this patent published?
Publication date Tue Feb 24 2026 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 2 related publications on this page (citations in our corpus or others sharing the same primary CPC).