US2018338979A1PendingUtilityA1

Method of Adjuvant Cancer Treatment

63
Assignee: NOVARTIS AGPriority: Sep 4, 2012Filed: Aug 7, 2018Published: Nov 29, 2018
Est. expirySep 4, 2032(~6.2 yrs left)· nominal 20-yr term from priority
A61P 35/00A61P 43/00A61P 17/00A61K 31/519A61K 31/506A61K 2300/00
63
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Claims

Abstract

The present invention provides a method of providing adjuvant treatment to a human patient which comprises administering to such a patient therapeutically effective doses of debrafenib and trametinib for a time period sufficient to increase relapse-free survival (RFS).

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A method of providing adjuvant treatment to a patient with a prior diagnosis of melanoma which has been resected, comprising the step of administering to such a patient therapeutically effective doses of dabrafenib and trametinib for a time period sufficient to increase relapse-free survival (RFS). 
     
     
         2 . The method of  claim 1 , wherein dabrafenib is administered at an amount of 150 mg twice a day. 
     
     
         3 . The method of  claim 1 , wherein trametinib is administered at an amount of 2 mg once daily. 
     
     
         4 . The method of  claim 1 , wherein the patient has a prior diagnosis of stage III melanoma which been resected. 
     
     
         5 . The method of  claim 1 , wherein the patient has a prior diagnosis of BRAF V600 mutation-positive melanoma which has been resected. 
     
     
         6 . A method of increasing relapse-free survival (RFS) of a patient after resection of melanoma, comprising the administration of a) dabrafenib and b) trametinib. 
     
     
         7 . The method of  claim 6 , wherein the melanoma is BRAF V600 mutation-positive. 
     
     
         8 . A composition comprising the combination of dabrafenib and trametinib for use in increasing relapse-free survival (RFS) in a patient after resection of melanoma.

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