US2014186469A1PendingUtilityA1
Pyrrolidine-1,2-dicarboxamide derivatives
Est. expirySep 10, 2028(~2.2 yrs left)· nominal 20-yr term from priority
A61P 9/00A61P 7/00A61P 43/00A61P 37/04A61P 9/10A61P 7/02A61P 9/12A61P 7/06A61P 37/06A61P 5/00A61P 37/08A61P 27/02A61P 29/00A61P 33/00A61P 25/00A61P 27/06A61P 31/12A61P 35/02A61P 35/00A61P 25/28A61P 1/16A61P 13/12A61P 21/00A61P 17/06A61P 21/04A61P 17/14A61P 17/00A61P 11/00A61P 11/06A61P 19/02A61P 17/02A61P 11/08A61P 19/10C07D 417/14A61K 31/4439A61K 45/06A61P 1/00A61K 31/427
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Claims
Abstract
The present invention relates to a compound of formula (I) or a salt thereof, wherein the substituents are as defined in the description, to compositions and use of the compounds in the treatment of diseases ameloriated by inhibition of phosphatidylinositol 3-kinase.
Claims
exact text as granted — not AI-modified1 . A method of treatment of a cancer of the breast or a tumor of the head or neck comprising administering to a subject in need thereof a therapeutically effective amount of a compound (S)-pyrrolidine-1,2-dicarboxylic acid 2-amide 1-({4-methyl-5-[2-(2,2,2-trifluoro-1,1-dimethyl-ethyl)-pyridin-4-yl]-thiazol-2-yl}-amide) or a pharmaceutically acceptable salt thereof and a therapeutically effective amount of an anticancer agent selected from the group consisting of fulvestrant, paclitaxel, cisplatin, vinblastine, tamoxifen, oxaliplatin, or a pharmaceutically acceptable salt thereof.
2 . The method according to claim 1 , wherein the anticancer agent is fulvestrant or a pharmaceutically acceptable salt thereof.
3 . The method according to claim 1 , wherein the anticancer agent is paclitaxel or a pharmaceutically acceptable salt thereof.Cited by (0)
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