Reyvow is owned by Eli Lilly And Co.
Reyvow contains Lasmiditan Succinate.
Reyvow has a total of 3 drug patents out of which 0 drug patents have expired.
Reyvow was authorised for market use on 31 January, 2020.
Reyvow is available in tablet;oral dosage forms.
Reyvow can be used as acute treatment of migraine.
Drug patent challenges can be filed against Reyvow from February, 2024.
The generics of Reyvow are possible to be released after 05 December, 2037.
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. | ||||
US7423050 | ELI LILLY AND CO | Pyridinoylpiperidines as 5-HT1F agonists |
Apr, 2025
(2 years from now) | |
US11053214 | ELI LILLY AND CO | Compositions and methods related to pyridinoylpiperidine 5-HT1F agonists |
Dec, 2037
(14 years from now) | |
These patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc). | ||||
US8748459 | ELI LILLY AND CO | Pyridinoylpiperidines as 5-HT1F agonists |
Mar, 2023
(a month from now) |
Exclusivity | Exclusivity Expiration |
---|---|
New Chemical Entity Exclusivity (NCE) | Jan 31, 2025 |
Drugs and Companies using LASMIDITAN SUCCINATE ingredient
NCE-1 date: February, 2024
Market Authorisation Date: 31 January, 2020
Treatment: Acute treatment of migraine
Dosage: TABLET;ORAL
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