Composition for Treating Prostate Cancer

US2016375091A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2016375091-A1
Application numberUS-201415105289-A
CountryUS
Kind codeA1
Filing dateDec 17, 2014
Priority dateDec 17, 2013
Publication dateDec 29, 2016
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.

The present invention relates to a composition for treating prostate cancer and, more specifically, to a composition for treating prostate cancer, which contains a peptide derived from telomerase and is effective in inhibiting growth and metastasis of prostate cancer cells. In addition, the present invention provides a composition and method for treating prostate cancer, wherein, when prostate cancer is treated, docetaxel and the peptide derived from telomerase are co-administered, thereby having a synergetic therapeutic effect compared with administration alone. Particularly, the present invention provides a treatment method useful for patients who do not have a sufficient anticancer effect merely through administration of docetaxel alone and patients who have hormone resistance.

First claim

Opening claim text (preview).

1 - 15 . (canceled) 16 . A method of treating prostate cancer comprising administering to a subject in need thereof the isolated peptide of SEQ ID NO: 1. 17 . The method according to claim 16 , wherein the prostate cancer has hormone tolerance. 18 . The method according to claim 16 , wherein the peptide is co-administered with an anti-cancer drug. 19 . The method according to claim 18 , wherein the anti-cancer drug is doetaxel or leuprolide acetate. 20 . The method according to claim 16 , wherein the peptide is co-administered with an adjuvant. 21 . The method according to claim 20 , wherein the adjuvant is macrophage colony-stimulating factor (GM-CSF). 22 . The method according to claim 19 , wherein the cytokine adjuvant macrophage colony-stimulating factor (GM-CSF) is further co-administered. 23 . The method according to claim 16 , wherein the patient has at least one of eotaxin and MIP 1 a at a serum concentration of at least 10% as high as the average concentration of eotaxin and MIP 1 a in all patients including the patient. 24 . The method according to claim 16 , wherein the peptide is administered at a daily dose of 0.1 ng/kg to 10 mg/kg. 25 . A method of treating prostate cancer comprising administering to a subject in need thereof a composition comprising the isolated peptide of SEQ ID NO:1. 26 . The method according to claim 26 , wherein the prostate cancer has hormone tolerance. 27 . The method according to claim 26 , wherein the composition is co-administered with an anti-cancer drug. 28 . The method according to claim 27 , wherein the anti-cancer drug is doetaxel or leuprolide acetate. 29 . The method according to claim 26 , wherein the composition is co-administered with an adjuvant. 30 . The method according to claim 28 , wherein the adjuvant macrophage colony-stimulating factor (GM-CSF) is further co-administered. 31 . The method according to claim 25 , wherein the patient has at least one of eotaxin and MIP1α at a serum concentration of at least 10% as high as the average concentration of eotaxin and MIP1α in all patients including the patient. 32 . The method according to claim 25 , wherein the composition is administered through oral, rectal, transdermal, intravenous, intramuscular, intraperitoneal, in the bone marrow, epidural, or subcutaneous routes. 33 . The method of claim 25 , wherein the composition comprises 0.01 g/L to 1 kg/L of the isolated peptide. 34 . The method of claim 25 , wherein the peptide is administered at a daily dose of 0.1 ng/kg to 10 mg/kg. 35 . A composition for treating prostate cancer comprising the isolated peptide of SEQ ID NO: 1 and at least one selected from the group consisting of a chemotherapeutic agent and an adjuvant.

Assignees

Inventors

Classifications

  • Antineoplastic agents · CPC title

  • Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00 · CPC title

  • specific for metastasis · CPC title

  • A61K38/10Primary

    Peptides having 12 to 20 amino acids {(A61K38/043 - A61K38/046 take precedence)} · CPC title

  • having four-membered rings, e.g. taxol · CPC title

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What does patent US2016375091A1 cover?
The present invention relates to a composition for treating prostate cancer and, more specifically, to a composition for treating prostate cancer, which contains a peptide derived from telomerase and is effective in inhibiting growth and metastasis of prostate cancer cells. In addition, the present invention provides a composition and method for treating prostate cancer, wherein, when prostate …
Who is the assignee on this patent?
Kim Sang Jae, Gemvax & Kael Co Ltd
What technology area does this patent fall under?
Primary CPC classification A61K38/10. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Thu Dec 29 2016 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).