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Rimegepant 75 MG (rimegepant-75-mg)
Rimegepant 75 MG (generic name: rimegepant-75-mg) is a CGRP receptor antagonist (gepant) drug developed by Pfizer Inc.. It is currently in preclinical development.
Rimegepant selectively antagonizes the calcitonin gene-related peptide (CGRP) receptor to block migraine pain signaling.
Rimegepant 75 MG is a small molecule that acts as an antagonist to the calcitonin gene-related peptide type 1 receptor. It is used to treat various types of migraines, including episodic migraine, menstrual migraine, migraine with aura, and migraine without aura.
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Baseline preclinical → approval rate
+5.0pp
Industry-wide preclinical drugs reach approval ~5% of the time (BIO/Informa 2023 industry benchmark across all therapeutic areas). -
CNS / neurology attrition
-3.0pp
CNS drugs have historically high Phase 3 failure rates (notably in Alzheimer disease + major depression). -
Big-pharma sponsor
+3.0pp
Pfizer Inc. is a top-20 pharma sponsor — historical approval rates run ~3pp above average due to scale, regulatory experience, and trial-design quality.
| Regulator | Country | Likely year | Lag vs FDA |
|---|---|---|---|
| FDA | US | 2036–2040 | — |
| EMA | EU | 2037–2041 | +0.7 yr |
| MHRA | GB | 2037–2041 | +0.7 yr |
| Health Canada | CA | 2037–2042 | +0.9 yr |
| TGA | AU | 2037–2042 | +1.2 yr |
| PMDA | JP | 2037–2042 | +1.5 yr |
| NMPA | CN | 2038–2043 | +2.3 yr |
| MFDS | KR | 2037–2042 | +1.4 yr |
| CDSCO | IN | 2037–2043 | +1.8 yr |
| ANVISA | BR | 2038–2043 | +2.3 yr |
Hover any row for the lag rationale. Lag estimates are reduced when the drug has FDA Breakthrough or EMA PRIME designation (sponsors file globally in parallel).
Estimate based on the BIO/Informa industry phase transition rates plus per-drug modifiers for therapeutic area, sponsor type, FDA designations, mechanism, and trial design. Per-jurisdiction lags from Tufts CSDD international approval studies. Not investment, clinical or regulatory advice. Methodology: /methodology#likelihood.
At a glance
| Generic name | rimegepant-75-mg |
|---|---|
| Sponsor | Pfizer Inc. |
| Drug class | CGRP receptor antagonist (gepant) |
| Target | Calcitonin gene-related peptide (CGRP) receptor |
| Therapeutic area | Neuroscience |
| Phase | preclinical |
Mechanism of action
Rimegepant works by blocking the CGRP receptor, a G-protein coupled receptor found on trigeminal sensory neurons and other pain-processing tissues. CGRP is a neuropeptide released during migraine attacks that triggers vasodilation, neuroinflammation, and pain signal amplification. By antagonizing this receptor, rimegepant interrupts the cascade of events that leads to migraine headache, photophobia, phonophobia, and associated symptoms. The drug crosses the blood-brain barrier as a small molecule, allowing it to act on both central and peripheral CGRP receptors. This mechanism differs from monoclonal antibody CGRP antagonists (like erenumab) by offering rapid oral absorption and faster symptom relief, making it suitable for acute migraine treatment rather than prevention alone.
Approved indications
Pipeline indications
- Acute treatment of migraine with or without aura — Phase 3
- Preventive treatment of episodic migraine — Phase 4
- Preventive treatment of menstrual migraine — Phase 3
- Acute treatment of migraine in pediatric subjects — Phase 3
- Acute treatment of chronic rhinosinusitis with and without nasal polyps — Phase 3
Common side effects
Competitive intelligence
For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape:
- Rimegepant 75 MG CI brief — competitive landscape report
- Rimegepant 75 MG updates RSS · CI watch RSS
- Pfizer Inc. portfolio CI
Frequently asked questions about Rimegepant 75 MG
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Related
- Drug class: All CGRP receptor antagonist (gepant) drugs
- Target: All drugs targeting Calcitonin gene-related peptide (CGRP) receptor
- Manufacturer: Pfizer Inc. — full pipeline
- Therapeutic area: All drugs in Neuroscience
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing