Relyvrio is owned by Amylyx.
Relyvrio contains Sodium Phenylbutyrate; Taurursodiol.
Relyvrio has a total of 5 drug patents out of which 0 drug patents have expired.
Relyvrio was authorised for market use on 29 September, 2022.
Relyvrio is available in for suspension;oral dosage forms.
Relyvrio can be used as treatment of amyotrophic lateral sclerosis (als) in adults.
Drug patent challenges can be filed against Relyvrio from 2026-09-29.
The generics of Relyvrio are possible to be released after 27 July, 2040.
Patent Number | Company | Patent Title | Patent Expiry | Activity Alert |
---|---|---|---|---|
These patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc). | ||||
US10857162 | AMYLYX | Compositions for improving cell viability and methods of use thereof |
Dec, 2033
(10 years from now) | |
US10251896 | AMYLYX | Compositions for improving cell viability and methods of use thereof |
Dec, 2033
(10 years from now) | |
US9872865 | AMYLYX | Compositions for improving cell viability and methods of use thereof |
Dec, 2033
(10 years from now) | |
US11071742 | AMYLYX | Compositions for improving cell viability and methods of use thereof |
Dec, 2033
(10 years from now) | |
US11583542 | AMYLYX | NA |
Jul, 2040
(17 years from now) |
Exclusivity | Exclusivity Expiration |
---|---|
New Chemical Entity Exclusivity (NCE) | Sep 29, 2027 |
Drugs and Companies using SODIUM PHENYLBUTYRATE; TAURURSODIOL ingredient
NCE-1 date: 2026-09-29
Market Authorisation Date: 29 September, 2022
Treatment: Treatment of amyotrophic lateral sclerosis (als) in adults
Dosage: FOR SUSPENSION;ORAL
9
United States
5
Korea, Republic of
4
Australia
4
Japan
3
China
2
European Union
1
Portugal
1
Slovenia
1
Croatia
1
ME
1
Hungary
1
Hong Kong
1
Poland
1
RS
1
Denmark
1
Canada
1
Lithuania
1
Spain
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