NDANASALSPRAY
Approved
Jan 2019
Lifecycle
Peak
Competitive Pressure
0/100
Clinical Trials
20
Data completeness
6/8 — Strong
TOSYMRA (sumatriptan) by GSK is serotonin 1b receptor agonists [moa]. First approved in 2019.
Drug data last refreshed 4h ago · AI intelligence enriched 1w ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
TOSYMRA is a nasal spray formulation of sumatriptan, a serotonin 1b/1d receptor agonist approved by the FDA in January 2019 for the acute treatment of migraine headaches. The drug works by constricting blood vessels around the brain and reducing substances in the body that cause headache, nausea, sensitivity to light and sound, and other migraine symptoms. It is designed for rapid intranasal delivery to patients experiencing migraine attacks.
$0.492MPart D
Peak5.1 years to LOEProduct is in peak commercial lifecycle with modest Medicare Part D penetration; commercial teams should expect stable but limited expansion opportunities given the mature nasal triptan market.
Mechanism of Action
Serotonin 1b Receptor Agonists
Pharmacologic Class:
Serotonin-1b and Serotonin-1d Receptor Agonist
Indications
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Clinical Trials (20)
A STUDY TO EVALUATE THE EFFECT OF PF-06651600 ON PHARMACOKINETICS OF SINGLE DOSE SUMATRIPTAN IN HEALTHY PARTICIPANTS.
Started Jun 2020
10 enrolled
Healthy Volunteers
Sofusa System With Sumatriptan (KC5010) Phase 1 Dose Escalation Safety and PK Study (KCC-SMT-002)
Started Jan 2018
19 enrolled
Migraine Disorders
A Study of Lasmiditan When Given With Sumatriptan in Healthy Participants
Started Oct 2017
40 enrolled
Healthy
Low-Dose Naltrexone and Acetaminophen Combination and Sumatriptan in the Acute Treatment of Migraine With Nausea
Started Jun 2017
36 enrolled
Migraine With and Without Aura
Effect of Single Oral Doses of Lasmiditan When Coadministered With Single Oral Doses of Sumatriptan in Healthy Participants
Started Mar 2017
42 enrolled
Migraine
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Data Sources
- Drug label: DailyMed / FDA
- Clinical trials: ClinicalTrials.gov
- Patent data: FDA Orange Book
- Spending data: CMS Medicare
The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.