IP Library › Granted Patent US 10,966,966
Granted Patent B2
US 10,966,966 · App. 17/028,640 · Granted Apr 6, 2021

Methods of treating gastrointestinal stromal tumors

Inventors: Rodrigo Ruiz Soto (Waltham, MA); Oliver Rosen (Waltham, MA); Jama Pitman (Waltham, MA)
Assignee: Deciphera Pharmaceuticals, LLC
A61K31/4375A61P35/00
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Quick Facts
Patent No.
US 10,966,966
App. No.
17/028,640
Granted
Apr 6, 2021
Kind
B2
Abstract

The present disclosure relates to methods of treating gastrointestinal stromal tumors to a subject in need thereof, comprising administering to the subject a therapeutically effective amount of ripretinib or a pharmaceutically acceptable salt thereof.

Claims (3)

1. A method of treating a patient suffering from an advanced gastrointestinal stromal tumor, comprising orally administering to the patient a 150 mg daily dose of ripretinib, wherein the patient's tumor has progressed from a first line administration of imatinib, a second line administration of sunitinib, and a third line administration of regorafenib, and wherein the patient achieves 6 months of progression free survival, as determined by mRECIST 1.1, after at least 28 days of the daily ripretinib administration.

2. The method of claim 1 , wherein if the patient suffers from a Grade 3 palmer-plantar erythrodysesthesia syndrome upon administration of the ripretinib, the method further comprises a) withholding administration of ripretinib for at least 7 days or until the patient has less than or equal to Grade 1 palmer-plantar erythrodysesthesia syndrome, then administering to the patient 100 mg daily ripretinib for at least 28 days.

3. The method of claim 1 , wherein if the patient suffers from a Grade 2 palmer-plantar erythrodysesthesia syndrome upon administration of the ripretinib, the method further comprises: a) withholding administration of ripretinib until the patient has less than or equal to Grade 1 palmer-plantar erythrodysesthesia syndrome or baseline; b) if the patient recovers from the palmer-plantar erythrodysesthesia syndrome within 7 days of withholding administration, then administering to the patient 150 mg daily ripretinib or c) if the patient has not recovered, then administering to the patient 100 mg daily ripretinib for at least 28 days.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 4, 2023
From: SOTO, RODRIGO RUIZ; ROSEN, OLIVER; PITMAN, JAMA
To: DECIPHERA PHARMACEUTICALS, LLC
Reel/Frame 062268/0955 →
Continuity (10)
Continuation PCTUS2020045876 · Aug 12, 2020
Provisional Application 63023921 · May 13, 2020
Provisional Application 63023936 · May 13, 2020
Provisional Application 62968927 · Jan 31, 2020
Provisional Application 62968945 · Jan 31, 2020
Provisional Application 62936018 · Nov 15, 2019
Provisional Application 62926281 · Oct 25, 2019
Provisional Application 62904198 · Sep 23, 2019
Provisional Application 62885797 · Aug 12, 2019
Related Publication 20210046059A1 · Feb 18, 2021
Cited By (12)
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