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topiramate, propranolol
Topiramate is an anticonvulsant that blocks voltage-dependent sodium channels and enhances the activity of GABA at the GABA_A receptor.
Topiramate is an anticonvulsant that blocks voltage-dependent sodium channels and enhances the activity of GABA at the GABA_A receptor. Used for Seizure prevention in patients with epilepsy, Migraine prevention.
At a glance
| Generic name | topiramate, propranolol |
|---|---|
| Sponsor | Johnson & Johnson Pharmaceutical Research & Development, L.L.C. |
| Drug class | Anticonvulsant |
| Target | Voltage-dependent sodium channels, GABA_A receptor |
| Modality | Small molecule |
| Therapeutic area | Neurology |
| Phase | Phase 3 |
Mechanism of action
Topiramate's mechanism of action is complex and multifaceted, involving the blockade of voltage-dependent sodium channels, which reduces the frequency of action potentials in neurons. Additionally, topiramate enhances the activity of GABA at the GABA_A receptor, which is the primary inhibitory neurotransmitter in the brain. This dual mechanism of action contributes to its anticonvulsant and neuroprotective effects.
Approved indications
- Seizure prevention in patients with epilepsy
- Migraine prevention
Common side effects
- Dizziness
- Headache
- Fatigue
- Nausea
- Drowsiness
Key clinical trials
- Comparative Effectiveness of Migraine Preventive Medications: The APT Comparison Study (PHASE4)
- ACT Therapy for HF Migraine (NA)
- Chinese Real-world Study of Treatment of Vestibular Migraine
- Quality Improvement and Practice Based Research in Neurology Using the EMR (PHASE4)
- Study of Human Non-Shivering Thermogenesis and Basal Metabolic Rate (PHASE2)
- Comparison of the Effectiveness of First-line Preventive Treatment of Migraine in Primary Care (PHASE4)
- Cognitive Side Effects of Commonly Prescribed Medications in Pediatric Migraine (NA)
- An Efficacy and Tolerability Study of Topiramate in Participants With Migraine (PHASE4)
Primary sources
Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.
| Source | Used for |
|---|---|
| ClinicalTrials.gov | Trial enrolment, design, endpoints, results |