Turalio is owned by Daiichi Sankyo Inc.
Turalio contains Pexidartinib Hydrochloride.
Turalio has a total of 12 drug patents out of which 0 drug patents have expired.
Turalio was authorised for market use on 02 August, 2019.
Turalio is available in capsule;oral dosage forms.
Turalio can be used as treatment of adult patients with symptomatic tenosynovial giant cell tumor (tgct) associated with severe morbidity or functional limitations and not amenable to improvement with surgery.
Drug patent challenges can be filed against Turalio from 2023-08-03.
The generics of Turalio are possible to be released after 24 July, 2038.
Patent Number | Company | Patent Title | Patent Expiry | Activity Alert |
---|---|---|---|---|
These patents protects the active chemical substance. Only patent owner can launch products that use this active substance. | ||||
US9169250 | DAIICHI SANKYO INC | Compounds modulating c-fms and/or c-kit activity and uses therefor |
Nov, 2027
(4 years from now) | |
US8722702 | DAIICHI SANKYO INC | Compounds modulating c-fms and/or c-kit activity and uses therefor |
Nov, 2027
(4 years from now) | |
US8404700 | DAIICHI SANKYO INC | Compounds modulating c-fms and/or c-kit activity and uses therefor |
Nov, 2027
(4 years from now) | |
US7893075 | DAIICHI SANKYO INC | Compounds modulating c-fms and/or c-kit activity and uses therefor |
May, 2033
(10 years from now) | |
US10730876 | DAIICHI SANKYO INC | Synthesis of a compound that modulates kinases |
May, 2036
(13 years from now) | |
US9802932 | DAIICHI SANKYO INC | Solid forms of a compound modulating kinases |
May, 2036
(13 years from now) | |
These patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc). | ||||
US8461169 | DAIICHI SANKYO INC | Compounds modulating c-fms and/or c-kit activity |
Apr, 2028
(5 years from now) | |
US9358235 | DAIICHI SANKYO INC | Kinase modulation, and indications therefor |
Jun, 2033
(10 years from now) | |
US10189833 | DAIICHI SANKYO INC | Solid forms of a compound modulating kinases |
May, 2036
(13 years from now) | |
US10435404 | DAIICHI SANKYO INC | Formulations of a compound modulating kinases |
Jul, 2038
(15 years from now) | |
US10961240 | DAIICHI SANKYO INC | Formulations of a compound modulating kinases |
Jul, 2038
(15 years from now) | |
US10941142 | DAIICHI SANKYO INC | Formulations of a compound modulating kinases |
Jul, 2038
(15 years from now) |
Exclusivity | Exclusivity Expiration |
---|---|
New Chemical Entity Exclusivity (NCE) | Aug 2, 2024 |
ODE* (ODE*) | Aug 2, 2026 |
Orphan Drug Exclusivity (ODE) | Aug 2, 2026 |
Drugs and Companies using PEXIDARTINIB HYDROCHLORIDE ingredient
NCE-1 date: 2023-08-03
Market Authorisation Date: 02 August, 2019
Treatment: Treatment of adult patients with symptomatic tenosynovial giant cell tumor (tgct) associated with severe morbidity or functional limitations and not amenable to improvement with surgery
Dosage: CAPSULE;ORAL
39
United States
10
Japan
7
China
7
European Union
6
Korea, Republic of
5
Australia
5
Brazil
5
Canada
4
Singapore
4
Spain
4
Taiwan, Province of China
3
Israel
3
South Africa
3
Hong Kong
2
Denmark
2
Mexico
2
Slovenia
2
Russia
2
Hungary
2
Colombia
2
Portugal
2
Malaysia
2
New Zealand
1
El Salvador
1
Lithuania
1
Philippines
1
Uruguay
1
Norway
1
Costa Rica
1
Croatia
1
Argentina
1
Guatemala
1
Cyprus
1
Peru
1
Poland
1
Chile
1
Ecuador
1
RS
1
Nicaragua
1
Ukraine
1
EA
900+ leading pharmaceutical companies are staying up-to-date with drug patents through Pharsight
Join them to stay ahead in capturing the next drug going generic