Cuvrior is owned by Orphalan.
Cuvrior contains Trientine Tetrahydrochloride.
Cuvrior has a total of 2 drug patents out of which 0 drug patents have expired.
Cuvrior was authorised for market use on 28 April, 2022.
Cuvrior is available in tablet;oral dosage forms.
Cuvrior can be used as a method for the treatment of adult patients with stable wilson’s disease who are de-coppered and tolerant to penicillamine.
The generics of Cuvrior are possible to be released after 03 May, 2039.
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. | ||||
US10988436 | ORPHALAN | Crystalline form of triethylenetetramine tetrahydrochloride and its pharmaceutical use |
May, 2039
(16 years from now) | |
These patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc). | ||||
US11072577 | ORPHALAN | Crystalline form of triethylenetetramine tetrahydrochloride and its pharmaceutical use |
May, 2039
(16 years from now) |
Exclusivity | Exclusivity Expiration |
---|---|
New Product (NP) | Apr 28, 2025 |
Orphan Drug Exclusivity (ODE) | Apr 28, 2029 |
Drugs and Companies using TRIENTINE TETRAHYDROCHLORIDE ingredient
Market Authorisation Date: 28 April, 2022
Treatment: A method for the treatment of adult patients with stable wilson’s disease who are de-coppered and tolerant to penicillamine
Dosage: TABLET;ORAL
4
United States
3
European Union
2
China
1
Germany
1
Singapore
1
Brazil
1
Japan
1
Argentina
1
Colombia
1
Morocco
1
EA
1
Canada
1
Spain
1
Australia
1
Korea, Republic of
1
Taiwan, Province of China
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