US2023398121A1PendingUtilityA1

Combination therapy for the treatment of cancer

Assignee: NOVARTIS AGPriority: Aug 14, 2013Filed: Aug 16, 2023Published: Dec 14, 2023
Est. expiryAug 14, 2033(~7.1 yrs left)· nominal 20-yr term from priority
A61K 31/4196A61K 45/06A61K 31/56A61K 31/551A61K 31/519A61K 31/506A61K 31/495A61K 31/436A61K 31/427A61P 35/00A61K 31/4439A61K 31/5377A61K 31/5513A61K 31/138A61K 31/565A61K 31/5685A61P 35/02A61P 43/00A61P 5/00A61P 5/32A61K 2300/00
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Claims

Abstract

The present disclosure relates to a pharmaceutical combination comprising (1) a first agent which is a CDK inhibitor or a pharmaceutically acceptable salt thereof and (2) a second agent which is an anti-hormonal agent or a pharmaceutically acceptable salt thereof. The present disclosure also relates to a pharmaceutical combination comprising (1) a first agent which is a CDK inhibitor or a pharmaceutically acceptable salt thereof, (2) a second agent which is an anti-hormonal agent or a pharmaceutically acceptable salt thereof, and (3) a third agent which is an agent that regulates the PI3K/Akt/mTOR pathway or a pharmaceutically acceptable salt thereof.

Claims

exact text as granted — not AI-modified
1 .- 42 . (canceled) 
     
     
         43 . A method of treating HR+ breast cancer in a human, comprising administering to the human Compound A1, or a pharmaceutically acceptable salt thereof: 
       
         
           
           
               
               
           
         
       
       and fulvestrant.

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