Transient protection of normal cells during chemotherapy

US2023381189A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2023381189-A1
Application numberUS-202318231091-A
CountryUS
Kind codeA1
Filing dateAug 7, 2023
Priority dateMar 15, 2013
Publication dateNov 30, 2023
Grant date

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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.

This invention is in the area of improved compounds, compositions and methods of transiently protecting healthy cells, and in particular hematopoietic stem and progenitor cells (HSPC) as well as renal cells, from damage associated with DNA damaging chemotherapeutic agents. In one aspect, improved protection of healthy cells is disclosed using disclosed compounds that act as highly selective and short, transiently-acting cyclin-dependent kinase 4/6 (CDK 4/6) inhibitors when administered to subjects undergoing DNA damaging chemotherapeutic regimens for the treatment of proliferative disorders.

First claim

Opening claim text (preview).

What is claimed is: 1 . A method of treating a human with triple negative breast cancer (TNBC) in need thereof comprising: administering to the human an effective amount of a selective CDK4/6 inhibitor of structure: or a pharmaceutically acceptable salt thereof; and, administering to the human an effective amount of a chemotherapeutic agent selected from the group consisting of carboplatin, cisplatin, gemcitabine, paclitaxel, doxorubicin, cyclophosphamide, and a combination thereof, wherein the CDK4/6 inhibitor is administered 4 hours or less prior to administration of the chemotherapeutic agent. 2 . The method of claim 1 , wherein the chemotherapeutic agent is carboplatin. 3 . The method of claim 1 , wherein the chemotherapeutic agent is cisplatin. 4 . The method of claim 1 , wherein the chemotherapeutic agent is paclitaxel. 5 . The method of claim 1 , wherein the chemotherapeutic agent is doxorubicin. 6 . The method of claim 1 , wherein the chemotherapeutic agent is cyclophosphamide. 7 . The method of claim 1 , wherein the chemotherapeutic agent is gemcitabine. 8 . A method of reducing chemotherapy-induced myelosuppression in a human receiving chemotherapy for the treatment of bladder cancer comprising administering to the human an effective amount of at least one DNA damaging chemotherapeutic agent and an effective amount of a CDK4/6 inhibitor of structure: or a pharmaceutically acceptable salt thereof; wherein the CDK4/6 inhibitor is administered 4 hours or less prior to administration of the DNA damaging chemotherapeutic agent. 9 . The method of claim 8 , wherein the CDK4/6 inhibitor is administered 1/2 hour or less prior to administration of the DNA damaging chemotherapeutic agent. 10 . The method of claim 8 , wherein the chemotherapeutic agent is administered to the human on day 1 every 21 days. 11 . The method of claim 8 , wherein the DNA damaging chemotherapeutic agent is administered to the human on days 1 and 8 every 21 days. 12 . The method of claim 8 , wherein the DNA damaging chemotherapeutic agent is selected from the group consisting of cisplatin, carboplatin, campothecin, doxorubicin, gemcitabine, and etoposide. 13 . The method of claim 12 , wherein the DNA damaging chemotherapeutic agent is cisplatin. 14 . The method of claim 12 , wherein the DNA damaging chemotherapeutic agent is carboplatin. 15 . The method of claim 12 , wherein the DNA damaging chemotherapeutic agent is campothecin. 16 . The method of claim 12 , wherein the chemotherapeutic agent is doxorubicin. 17 . The method of claim 12 , wherein the chemotherapeutic agent is gemcitabine. 18 . The method of claim 12 , wherein the chemotherapeutic agent is etoposide.

Assignees

Inventors

Classifications

  • Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner (non-active ingredients are additionally classified in A61K47/00) · CPC title

  • A61K31/527Primary

    spiro-condensed · CPC title

  • C07D487/14Primary

    Ortho-condensed systems · CPC title

  • Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca · CPC title

  • ortho- or peri-condensed with heterocyclic rings · CPC title

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What does patent US2023381189A1 cover?
This invention is in the area of improved compounds, compositions and methods of transiently protecting healthy cells, and in particular hematopoietic stem and progenitor cells (HSPC) as well as renal cells, from damage associated with DNA damaging chemotherapeutic agents. In one aspect, improved protection of healthy cells is disclosed using disclosed compounds that act as highly selective and…
Who is the assignee on this patent?
G1 Therapeutics Inc
What technology area does this patent fall under?
Primary CPC classification A61K31/527. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Thu Nov 30 2023 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).