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Qinlock patents expiration

Can you believe QINLOCK received compensation for the extended wait time during the regulatory approval process?
Drug Patent Number Company Drug Patent Title Drug Patent Expiry Activity Alert
These drug patents protects the active chemical substance. Only drug patent owner can launch products that use this active substance.
US8188113 DECIPHERA PHARMS Dihydropyridopyrimidinyl, dihydronaphthyidinyl and related compounds useful as kinase inhibitors for the treatment of proliferative diseases
Jul, 2030

(6 years from now)

US8461179 DECIPHERA PHARMS Dihydronaphthyridines and related compounds useful as kinase inhibitors for the treatment of proliferative diseases
Jun, 2032

(8 years from now)

These drug patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc).
USRE48731 DECIPHERA PHARMS Dihydronaphthyridines and related compounds useful as kinase inhibitors for the treatment of proliferative diseases
Jun, 2032

(8 years from now)

US11576904 DECIPHERA PHARMS NA
Aug, 2040

(16 years from now)

US11266635 DECIPHERA PHARMS Methods of treating gastrointestinal stromal tumors
Aug, 2040

(16 years from now)

US10966966 DECIPHERA PHARMS Methods of treating gastrointestinal stromal tumors
Aug, 2040

(16 years from now)

US11426390 DECIPHERA PHARMS Methods of treating gastrointestinal stromal tumors
Aug, 2040

(16 years from now)

US11344536 DECIPHERA PHARMS Methods of treating gastrointestinal stromal tumors
Aug, 2040

(16 years from now)

US11529336 DECIPHERA PHARMS Methods of treating gastrointestinal stromal tumors
Aug, 2040

(16 years from now)

US11534432 DECIPHERA PHARMS Methods of treating gastrointestinal stromal tumors
Aug, 2040

(16 years from now)

US11433056 DECIPHERA PHARMS Methods of treating gastrointestinal stromal tumors
Aug, 2040

(16 years from now)

US11185535 DECIPHERA PHARMS Amorphous kinase inhibitor formulations and methods of use thereof
Dec, 2040

(17 years from now)

US11612591 DECIPHERA PHARMS NA
Dec, 2040

(17 years from now)

US11395818 DECIPHERA PHARMS Compositions of 1-(4-bromo-5-(1-ethyl-7-(methylamino)-2-oxo-1,2-dihydro-1,6-naphthyridin-3-yl)-2-fluorophenyl)-3-phenylurea
Dec, 2040

(17 years from now)

US11576903 DECIPHERA PHARMS NA
Dec, 2040

(17 years from now)

Qinlock is owned by Deciphera Pharms.

Qinlock contains Ripretinib.

Qinlock has a total of 15 drug patents out of which 0 drug patents have expired.

Qinlock was authorised for market use on 15 May, 2020.

Qinlock is available in tablet;oral dosage forms.

Qinlock can be used as treatment of advanced gastrointestinal stromal tumor in patients previously administered at least three tyrosine kinase inhibitors, where one of the kinase inhibitors is imatinib, treatment of gastrointestinal stromal tumors in patients suffering from a grade 3 adverse reaction while being administered ripretinib daily, method of treating gastrointestinal stromal tumors in patients suffering from grade 2 or grade 3 myalgia while being administered ripretinib daily, treatment of advanced gastrointestinal stromal tumor in patients having progressed from a first line administration of imatinib, a second line administration of sunitinib, and a third line administration of regorafenib, treatment of gastrointestinal stromal tumors in patients being treated concurrently with a cyp3a4 inhibitor, treatment of gastrointestinal stromal tumor, treatment of gastrointestinal stromal tumors in patients suffering from hypertension, treatment of gastrointestinal stromal tumors in patients suffering from palmer-planter erythrodysesthesia syndrome, treatment of gastrointestinal stromal tumors in patients suffering from grade 2 or grade 3 arthralgia while being administered ripretinib daily.

Drug patent challenges can be filed against Qinlock from 2024-05-15.

The generics of Qinlock are possible to be released after 30 December, 2040.

Drug Exclusivity Drug Exclusivity Expiration
New Chemical Entity Exclusivity (NCE) May 15, 2025
Orphan Drug Exclusivity (ODE) May 15, 2027

Drugs and Companies using RIPRETINIB ingredient

NCE-1 date: 2024-05-15

Market Authorisation Date: 15 May, 2020

Treatment: Treatment of gastrointestinal stromal tumor; Treatment of gastrointestinal stromal tumors in patients suffering from grade 2 or grade 3 arthralgia while being administered ripretinib daily; Treatment ...

Dosage: TABLET;ORAL

More Information on Dosage

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