Tukysa is owned by Seagen.
Tukysa contains Tucatinib.
Tukysa has a total of 6 drug patents out of which 0 drug patents have expired.
Tukysa was authorised for market use on 17 April, 2020.
Tukysa is available in tablet;oral dosage forms.
Tukysa can be used as combination treatment of colorectal cancer including ras wild-type her2 (erbb2)-positive or -overexpressing unresectable or metastatic colorectal cancer, treatment of breast cancer including her2 (erbb2)-positive or -overexpressing breast cancer.
Drug patent challenges can be filed against Tukysa from 2024-04-17.
The generics of Tukysa are possible to be released after 27 April, 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. | ||||
US7452895 | SEAGEN | Quinazoline analogs as receptor tyrosine kinase inhibitors |
Nov, 2024
(1 year, 7 months from now) | |
US8648087 | SEAGEN | N4-phenyl-quinazoline-4-amine derivatives and related compounds as ErbB type I receptor tyrosine kinase inhibitors for the treatment of hyperproliferative diseases |
Apr, 2031
(8 years from now) | |
These patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc). | ||||
US9693989 | SEAGEN | N4-phenyl-quinazoline-4-amine derivatives and related compounds as ErbB type I receptor tyrosine kinase inhibitors for the treatment of hyperproliferative diseases |
May, 2027
(4 years from now) | |
US9457093 | SEAGEN | Solid dispersions of a ERB2 (HER2) inhibitor |
Oct, 2032
(9 years from now) | |
US11504370 | SEAGEN | NA |
Mar, 2033
(10 years from now) | |
US11207324 | SEAGEN | Treatment of HER2 positive cancers |
Apr, 2038
(15 years from now) |
Exclusivity | Exclusivity Expiration |
---|---|
Orphan Drug Exclusivity (ODE) | Apr 17, 2027 |
New Chemical Entity Exclusivity (NCE) | Apr 17, 2025 |
New Indication (I) | Jan 19, 2026 |
Drugs and Companies using TUCATINIB ingredient
NCE-1 date: 2024-04-17
Market Authorisation Date: 17 April, 2020
Treatment: Treatment of breast cancer including her2 (erbb2)-positive or -overexpressing breast cancer; Combination treatment of colorectal cancer including ras wild-type her2 (erbb2)-positive or -overexpressing unresectable or metastatic colorectal cancer
Dosage: TABLET;ORAL
33
United States
11
China
10
Japan
10
Australia
8
European Union
7
Russia
7
Korea, Republic of
7
Israel
6
Portugal
6
Spain
6
New Zealand
6
Canada
6
Slovenia
6
Poland
6
Denmark
5
Brazil
5
Cyprus
4
Taiwan, Province of China
4
Hong Kong
4
Hungary
4
Ukraine
3
Singapore
3
Norway
3
Mexico
3
South Africa
3
Lithuania
3
Chile
2
Germany
2
Malaysia
2
Croatia
2
Colombia
2
Austria
2
RS
1
Turkey
1
Costa Rica
1
Philippines
1
Argentina
1
Luxembourg
1
Iceland
1
ME
1
Netherlands
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