Rimegepant Sulfate
FDA-approved product (tablet, orally disintegrating, oral), marketed as Nurtec Odt.
- Registered studies
- 50+
- Lab records
- 0
- Pathogens at ≥40%
- 4 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Migraine disorder
Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗
- WHO therapeutic group
- Calcitonin gene-related peptide (cgrp) antagonists
- Anti-infective classification
- Not classified as an anti-infective.
Repurposing investigation
This medicine is being investigated here for AI-predicted antimicrobial activity against M. tuberculosis, MRSA, E. coli and K. pneumoniae. It was surfaced computationally for further investigation; it is not an established treatment for these infections.
AI-predicted activity
AI prediction · nothing measured- MRSA64.7% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- E. coli61.6% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- K. pneumoniae40.9% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- M. tuberculosis60.6% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
A model’s estimate of laboratory activity against each pathogen species. It is not clinical effectiveness.
Evidence
Clinical and experimental
Documented evidenceClinical
50+registered studies name this medicine, for any condition. The registry search keeps the first 50, so there may be more. See them below.
Experimental
No evidence found
No laboratory measurement against the four pathogens in the ChEMBL records loaded here.
Docking
Computational · nothing measuredDihydrofolate reductase ↗ (E. coli)
Not yet docked: queued in the docking rundetails
KPC-2 carbapenemase ↗ (K. pneumoniae)
Not yet docked: queued in the docking rundetails
Enoyl-ACP reductase (InhA) ↗ (M. tuberculosis)
Not yet docked: queued in the docking rundetails
Dihydrofolate reductase ↗ (MRSA)
Not yet docked: queued in the docking rundetails
AutoDock Vina, one experimentally solved protein per pathogen. This project’s screening target is -7.0 kcal/mol, its own mark rather than a universal cutoff. A docking score is a structural hypothesis, not proof of binding, and requires experimental validation.
Other medicines to investigate
AI prediction · nothing measuredOther repurposing candidates: approved medicines besides Rimegepant Sulfate with AI-predicted activity ≥40% against the chosen pathogen, leaving out existing antimicrobials. They are computational candidates for further investigation, not alternatives and not recommendations.
Sorted by AI-predicted activity, high to low. The order is not a ranking of which medicine is better.
- FurazolidoneExisting use: Other antiinfectives and antiseptics91.4% AI-predicted activityagainst M. tuberculosisLab records exist49 registered studies
- TriflupromazineExisting use: Psychosis90.6% AI-predicted activityagainst M. tuberculosisNo documented evidence found
- ValdecoxibExisting use: Dysmenorrhea, Osteoarthritis, Rheumatic disease and 1 more88.6% AI-predicted activityagainst M. tuberculosisLab records exist31 registered studies
- CelecoxibExisting use: Ankylosing spondylitis, Cancer, Colorectal neoplasm and 15 more87.6% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
- Dorzolamide HydrochlorideExisting use: Glaucoma, Ocular hypertension, Open-angle glaucoma86.8% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
- MethazolamideExisting use: Glaucoma, Open-angle glaucoma85.6% AI-predicted activityagainst M. tuberculosisLab records exist11 registered studies
- AcetazolamideExisting use: Altitude sickness, Angle-closure glaucoma, Congestive heart failure and 5 more85.2% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
- Trifluoperazine HydrochlorideExisting use: Anxiety disorder, Mental or behavioural disorder, Psychosis and 1 more84.6% AI-predicted activityagainst M. tuberculosis1 registered study
- TriclosanExisting use: Phenol and derivatives, Medicated dressings with antiinfectives84.2% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
- NitrofurazoneExisting use: Eye infection, Leishmaniasis, Trypanosomiasis84.0% AI-predicted activityagainst M. tuberculosis8 registered studies
- BrinzolamideExisting use: Glaucoma, Ocular hypertension, Open-angle glaucoma83.8% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
- ZonisamideExisting use: Epilepsy, Focal-onset seizure, Partial epilepsy and 1 more82.8% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
Registered studies
A registration describes a study; it does not establish a positive result.
Comparison of Patient-reported Outcomes for Rimegepant and Triptans in the 2023 US National Health and Wellness Survey
NCT06680206 · start 2024-10-10
Registered record
- Registry ID
- NCT06680206
- Conditions
- Migraine
- Interventions
- Rimegepant; Triptans
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2024-10-10
- Completion
- 2024-11-20
- Enrolment
- 1,395
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMigraineInterventionRimegepant; TriptansPhaseNot recordedRegistry statusCompletedA Comparison of Nurtec ODT to Maxalt MLT-ODT in Adult ED Patients With Migraine Headache
NCT06473597 · start 2024-09-01
Registered record
- Registry ID
- NCT06473597
- Conditions
- Migraine
- Interventions
- Rimegepant; Rizatriptan Benzoate
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Recruiting
- Start
- 2024-09-01
- Completion
- 2026-12-31
- Enrolment
- 80
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMigraineInterventionRimegepant; Rizatriptan BenzoatePhasePhase 4Registry statusRecruitingARISE-A Chinese Real-world Study of Rimegepant for the Acute Treatment of Migraine
NCT06439628 · start 2024-08-27
Registered record
- Registry ID
- NCT06439628
- Conditions
- Migraine
- Interventions
- Rimegepant
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Active not recruiting
- Start
- 2024-08-27
- Completion
- 2027-06-28
- Enrolment
- 3,000
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMigraineInterventionRimegepantPhaseNot recordedRegistry statusActive not recruitingComparison of Rimegepant and Placebo for Pain in IBS
NCT06221111 · start 2024-06-06
Registered record
- Registry ID
- NCT06221111
- Conditions
- Irritable Bowel Syndrome
- Interventions
- Rimegepant 75 MG [Nurtec]
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2024-06-06
- Completion
- 2025-06-03
- Enrolment
- 39
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionIrritable Bowel SyndromeInterventionRimegepant 75 MG [Nurtec]PhasePhase 2Registry statusCompletedMigraine Medication Effects on Urinary Symptoms
NCT06212661 · start 2024-04-05
Registered record
- Registry ID
- NCT06212661
- Conditions
- Overactive Bladder; Bladder Pain Syndrome; Migraine Disorders; Overactive Bladder Syndrome; Overactive Detrusor; Migraine; Interstitial Cystitis
- Interventions
- Ubrogepant; Rimegepant; Atogepant; Eptinezumab; Fremanezumab; Galcanezumab; Erenumab; Botulinum toxin A
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Enrolling by invitation
- Start
- 2024-04-05
- Completion
- 2026-12
- Enrolment
- 200
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionOveractive Bladder; Bladder Pain Syndrome; Migraine Disorders; Overactive Bladder Syndrome +3 moreInterventionUbrogepant; Rimegepant; Atogepant; Eptinezumab +4 morePhaseNot recordedRegistry statusEnrolling by invitationRimegepAnt effectIvenesS and tolErability as Migraine Preventive Treatment
NCT06409832 · start 2024-03-26
Registered record
- Registry ID
- NCT06409832
- Conditions
- Migraine; Migraine With Aura; Migraine Without Aura
- Interventions
- Rimegepant 75 mg
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Recruiting
- Start
- 2024-03-26
- Completion
- 2027-09
- Enrolment
- 100
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMigraine; Migraine With Aura; Migraine Without AuraInterventionRimegepant 75 mgPhaseNot recordedRegistry statusRecruitingA Registry Study on Rimegepant for the Treatment of Migraine Participants in Guangdong-Hong Kong-Macao Greater Bay Area
NCT06221267 · start 2024-01-26
Registered record
- Registry ID
- NCT06221267
- Conditions
- Migraine
- Interventions
- Rimegepant
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2024-01-26
- Completion
- 2024-06-30
- Enrolment
- 120
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMigraineInterventionRimegepantPhaseNot recordedRegistry statusCompletedA Study to Learn About the Safety and Effects of Rimegepant to Prevent Migraine in Chinese Subjects.
NCT05810038 · start 2023-05-15
Registered record
- Registry ID
- NCT05810038
- Conditions
- Migraine
- Interventions
- Rimegepant; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2023-05-15
- Completion
- 2025-12-10
- Enrolment
- 787
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMigraineInterventionRimegepant; PlaceboPhasePhase 3Registry statusCompletedA Prospective Real World Study of Rimegepant in the Treatment of Migraine
NCT05709106 · start 2023-01-11
Registered record
- Registry ID
- NCT05709106
- Conditions
- Migraine
- Interventions
- Rimegepant 75 MG
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2023-01-11
- Completion
- 2025-04-09
- Enrolment
- 173
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMigraineInterventionRimegepant 75 MGPhaseNot recordedRegistry statusCompletedEfficacy and Tolerability of Rimegepant for the Prevention of Migraine in Adults With History of Inadequate Response to Oral Preventive Medications
NCT05518123 · start 2022-11-07
Registered record
- Registry ID
- NCT05518123
- Conditions
- Migraine
- Interventions
- Rimegepant; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2022-11-07
- Completion
- 2025-07-08
- Enrolment
- 962
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMigraineInterventionRimegepant; PlaceboPhasePhase 4Registry statusCompletedEfficacy and Tolerability of Rimegepant for the Acute Treatment of Migraine in Adults Unsuitable for Triptan Use
NCT05509400 · start 2022-10-18
Registered record
- Registry ID
- NCT05509400
- Conditions
- Migraine
- Interventions
- Rimegepant; Placebo; Rimegepant
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2022-10-18
- Completion
- 2025-06-10
- Enrolment
- 813
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMigraineInterventionRimegepant; Placebo; RimegepantPhasePhase 4Registry statusCompletedEfficacy and Safety Study of Rimegepant for the Acute Treatment of Migraine in Japanese Subjects (Japan Only)
NCT05399459 · start 2022-08-09
Registered record
- Registry ID
- NCT05399459
- Conditions
- Migraine
- Interventions
- Rimegepant 25 MG; Rimegepant 75 MG; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2022-08-09
- Completion
- 2024-01-19
- Enrolment
- 897
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMigraineInterventionRimegepant 25 MG; Rimegepant 75 MG; PlaceboPhasePhase 3Registry statusCompletedEfficacy and Safety Study of Rimegepant for Migraine Prevention in Japanese Subjects (Japan Only)
NCT05399485 · start 2022-08-09
Registered record
- Registry ID
- NCT05399485
- Conditions
- Migraine
- Interventions
- Rimegepant; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2022-08-09
- Completion
- 2024-11-07
- Enrolment
- 496
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMigraineInterventionRimegepant; PlaceboPhasePhase 3Registry statusCompletedA Study to Learn About the Long-term Safety of Rimegepant for the Acute Treatment of Migraine in Chinese Participants
NCT05371652 · start 2022-05-19
Registered record
- Registry ID
- NCT05371652
- Conditions
- Acute Migraine
- Interventions
- Rimegepant 75mg Orally Disintegrating Tablets (ODT)
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2022-05-19
- Completion
- 2024-02-06
- Enrolment
- 241
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAcute MigraineInterventionRimegepant 75mg Orally Disintegrating Tablets (ODT)PhasePhase 3Registry statusCompletedEvaluation of the Efficacy of Diclofenac Potassium and Rimegepant for the Acute Treatment of Migraine
NCT05211154 · start 2022-05-05
Registered record
- Registry ID
- NCT05211154
- Conditions
- Migraine With Aura; Migraine Without Aura
- Interventions
- Diclofenac Potassium 50Mg/Pkt Oral Pwdr; Rimegepant 75 MG
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Terminated
- Start
- 2022-05-05
- Completion
- 2025-04-30
- Enrolment
- 300
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMigraine With Aura; Migraine Without AuraInterventionDiclofenac Potassium 50Mg/Pkt Oral Pwdr; Rimegepant 75 MGPhasePhase 4Registry statusTerminated