Lasmiditan
As of the edition of 20 October 2026, Lasmiditan is a small molecule: marketed, first approved in 2020 (US); acts on HTR1F; US protection ends in 2037.
Sources: FDA Orange Book and Purple Book, other approval registers, ClinicalTrials.gov, ChEMBL.
The drug
- Status
- Marketed; latest approval 2022
- Kind
- Small molecule
- Brand name
- Reyvow
- First approved
- 31 January 2020 (US)
- Approvals on record
- 6 in 3 regions
- Holder of the most recent approval
- Eli Lilly; 2 holders in all
- Registered trials
- 33, 2 stopped early
- Disease areas
- Nervous system; Chemically induced; Mental health
US protection
US protection ends in 2037.
The last listed US drug-substance patent ends in 2037. The application that gives this date is held by Eli Lilly.
This is the US only, and it is not the date generics or biosimilars can enter.
The exact date and the listings behind it
In the product6 listings count towards this date. The exact date and each listing are in the product.
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Companies that need a new molecule because of this drug
1 company on route B because of this drug.
Companies on route B for this drug
In the product1 company is on route B because of Lasmiditan.
See the 1 company on route B for this drug, with the facts behind eachRequest access. Nothing is shown until you do.
Target
| Gene | Protein | UniProt |
|---|---|---|
| HTR1F | 5-hydroxytryptamine receptor 1F | P30939 |
Registered trials
| Phase | Trials | Completed | Active | Stopped early |
|---|---|---|---|---|
| Phase not stated | 1 | 1 | 0 | 0 |
| Phase 1 | 22 | 21 | 0 | 0 |
| Phase 2 | 3 | 3 | 0 | 0 |
| Phase 3 | 7 | 5 | 0 | 2 |
| All trials | 33 |
Who has held its approvals
| Company | Role | Years |
|---|---|---|
| Eli Lilly | Originator, Applicant and Lead sponsor of trials | 2006 to now |