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.
- Mefloquine HydrochlorideExisting use: Malaria, Plasmodium falciparum malaria, Plasmodium vivax malaria81.8% AI-predicted activityagainst M. tuberculosisLab records exist8 registered studies
- KetoconazoleExisting use: Adrenal gland disease, Blastomycosis, Cushing syndrome and 3 more81.2% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
- LevoketoconazoleExisting use: Adrenal gland disease, Adrenal gland hyperfunction, Cushing syndrome81.2% AI-predicted activityagainst M. tuberculosis6 registered studies
- Fluphenazine DecanoateExisting use: Mental or behavioural disorder, Psychosis80.7% AI-predicted activityagainst M. tuberculosis4 registered studies
- Fluphenazine EnanthateExisting use: Mental or behavioural disorder, Psychosis80.7% AI-predicted activityagainst M. tuberculosisNo documented evidence found
- NifurtimoxExisting use: American trypanosomiasis, Chagas disease, Leishmaniasis and 1 more78.4% AI-predicted activityagainst M. tuberculosis19 registered studies
- Fluphenazine HydrochlorideExisting use: Mental or behavioural disorder, Psychosis77.8% AI-predicted activityagainst M. tuberculosis5 registered studies
- NitazoxanideExisting use: Amebiasis, Diarrhea77.8% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
- TopiramateExisting use: Epilepsy, Lennox-Gastaut syndrome, Migraine disorder and 1 more77.4% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
- TrabectedinExisting use: Cancer, Dedifferentiated liposarcoma, Leiomyosarcoma and 7 more76.8% AI-predicted activityagainst M. tuberculosis50+ registered studies
- Chlorpromazine HydrochlorideExisting use: Conduct disorder, Mental or behavioural disorder, Nausea and vomiting and 3 more75.0% AI-predicted activityagainst M. tuberculosis33 registered studies
- ProchlorperazineExisting use: Anxiety disorder, Nausea and vomiting, Psychosis and 1 more74.1% AI-predicted activityagainst M. tuberculosis50+ registered studies
Registered studies
A registration describes a study; it does not establish a positive result.
Open Label Safety Study in Acute Treatment of Migraine
NCT03266588 · start 2017-08-30
Registered record
- Registry ID
- NCT03266588
- Conditions
- Migraine, With or Without Aura
- Interventions
- Rimegepant
- Study type
- INTERVENTIONAL
- Phase
- Phase 2 / Phase 3
- Registry status
- Completed
- Start
- 2017-08-30
- Completion
- 2019-07-15
- Enrolment
- 3,019
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMigraine, With or Without AuraInterventionRimegepantPhasePhase 2 / Phase 3Registry statusCompletedSafety and Efficacy in Adult Subjects With Acute Migraines
NCT03237845 · start 2017-07-27
Registered record
- Registry ID
- NCT03237845
- Conditions
- Migraine, With or Without Aura
- Interventions
- Rimegepant; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2017-07-27
- Completion
- 2018-01-31
- Enrolment
- 1,499
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMigraine, With or Without AuraInterventionRimegepant; PlaceboPhasePhase 3Registry statusCompletedStudy to Evaluate the PK of BMS-927711 in Patient With Migraine During Acute Migraine and Non-migraine Condition
NCT01445067 · start 2011-11
Registered record
- Registry ID
- NCT01445067
- Conditions
- Migraine
- Interventions
- BMS-927711 (CGRP Antagonist); BMS-927711 (CGRP Antagonist)
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2011-11
- Completion
- 2012-09
- Enrolment
- 48
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMigraineInterventionBMS-927711 (CGRP Antagonist); BMS-927711 (CGRP Antagonist)PhasePhase 1Registry statusCompletedDose Ranging Study of Rimegepant (BMS-927711) for the Acute Treatment of Migraine
NCT01430442 · start 2011-10
Registered record
- Registry ID
- NCT01430442
- Conditions
- Migraine; Acute Treatment of Migraine
- Interventions
- Rimegepant; Placebo; Sumatriptan
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2011-10
- Completion
- 2012-05
- Enrolment
- 1,026
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMigraine; Acute Treatment of MigraineInterventionRimegepant; Placebo; SumatriptanPhasePhase 2Registry statusCompletedAn Open-label, Intermediate Size, Expanded Access Study of BHV-3000 in the Acute Treatment of Migraine
NCT03934086
Registered record
- Registry ID
- NCT03934086
- Conditions
- Migraine
- Interventions
- rimegepant
- Study type
- EXPANDED_ACCESS
- Phase
- Not recorded
- Registry status
- No longer available
- Start
- Not recorded
- Completion
- Not recorded
- Enrolment
- Not recorded
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMigraineInterventionrimegepantPhaseNot recordedRegistry statusNo longer available