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 E. coli, MRSA, K. pneumoniae and M. tuberculosis. 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.
- Trimetrexate GlucuronateExisting use: Other agents against amoebiasis and other protozoal diseases88.6% AI-predicted activityagainst E. coliLab records exist17 registered studies
- Folic AcidExisting use: Acne, Anemia, Anemia (phenotype) and 8 more87.0% AI-predicted activityagainst E. coliLab records exist50+ registered studies
- MethotrexateExisting use: Acute lymphoblastic leukemia, Adenoma, Arthritis and 21 more86.8% AI-predicted activityagainst E. coliLab records exist50+ registered studies
- PralatrexateExisting use: Cancer, Mature T-cell and NK-cell non-Hodgkin lymphoma, Neoplasm and 2 more82.2% AI-predicted activityagainst E. coli44 registered studies
- TriclosanExisting use: Phenol and derivatives, Medicated dressings with antiinfectives81.0% AI-predicted activityagainst E. coliLab records exist50+ registered studies
- Leucovorin CalciumExisting use: Osteosarcoma67.6% AI-predicted activityagainst E. coli50+ registered studies
- LevoleucovorinExisting use: Anemia, Colorectal adenocarcinoma, Colorectal cancer and 3 more67.6% AI-predicted activityagainst E. coli50+ registered studies
- PyrimethamineExisting use: Malaria, Toxoplasmosis64.6% AI-predicted activityagainst E. coliLab records exist50+ registered studies
- Copanlisib DihydrochlorideExisting use: Follicular lymphoma, Neoplasm, Neoplasm of mature B-cells63.5% AI-predicted activityagainst E. coli10 registered studies
- AfamelanotideExisting use: Erythropoietic protoporphyria62.6% AI-predicted activityagainst E. coli23 registered studies
- Histrelin AcetateExisting use: Neoplasm, Prostate adenocarcinoma, Prostate cancer61.6% AI-predicted activityagainst E. coli13 registered studies
- Pafolacianine SodiumExisting use: Other diagnostic agents61.4% AI-predicted activityagainst E. coli1 registered study
Registered studies
A registration describes a study; it does not establish a positive result.
Safety and Efficacy of BHV-3000 (Rimegepant) Orally Disintegrating Tablet for Acute Treatment of Temporomandibular Disorders
NCT05262517 · start 2022-05-05
Registered record
- Registry ID
- NCT05262517
- Conditions
- Temporomandibular Disorders (TMD)
- Interventions
- Rimegepant; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Terminated
- Start
- 2022-05-05
- Completion
- 2023-05-18
- Enrolment
- 126
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionTemporomandibular Disorders (TMD)InterventionRimegepant; PlaceboPhasePhase 3Registry statusTerminatedSafety and Tolerability Study of Daily Dosing Rimegepant in Episodic Migraine Prevention
NCT05207865 · start 2022-03-15
Registered record
- Registry ID
- NCT05207865
- Conditions
- Migraine; Episodic Migraine; Phonophobia; Photophobia
- Interventions
- Rimegepant
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2022-03-15
- Completion
- 2024-07-02
- Enrolment
- 441
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMigraine; Episodic Migraine; Phonophobia; PhotophobiaInterventionRimegepantPhasePhase 4Registry statusCompletedEfficacy and Safety Study of Rimegepant in Episodic Migraine Prevention With Multiple Dosing Regimens
NCT05217927 · start 2022-03-04
Registered record
- Registry ID
- NCT05217927
- Conditions
- Migraine
- Interventions
- Rimegepant 75mg daily dosing; Rimegepant 75mg every other day dosing; Placebo comparator dosing
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2022-03-04
- Completion
- 2024-12-11
- Enrolment
- 1,415
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMigraineInterventionRimegepant 75mg daily dosing; Rimegepant 75mg every other day dosing; Placebo comparator dosingPhasePhase 4Registry statusCompletedEfficacy and Safety Study of Rimegepant for the Preventative Treatment of Migraine in Pediatric Subjects
NCT05156398 · start 2022-02-28
Registered record
- Registry ID
- NCT05156398
- Conditions
- Migraine
- Interventions
- Rimegepant; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Recruiting
- Start
- 2022-02-28
- Completion
- 2032-11-27
- Enrolment
- 640
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMigraineInterventionRimegepant; PlaceboPhasePhase 3Registry statusRecruitingSafety and Efficacy of BHV-3000 (Rimegepant) Orally Disintegrating Tablet for the Acute Treatment of Chronic Rhinosinusitis
NCT05248997 · start 2022-02-17
Registered record
- Registry ID
- NCT05248997
- Conditions
- Chronic Rhinosinusitis (CRS) With and Without Nasal Polyps
- Interventions
- rimegepant 75 mg ODT; Matching placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2022-02-17
- Completion
- 2024-04-02
- Enrolment
- 261
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionChronic Rhinosinusitis (CRS) With and Without Nasal PolypsInterventionrimegepant 75 mg ODT; Matching placeboPhasePhase 3Registry statusCompletedStudy of Pregnancy Outcomes in Women Exposed to Rimegepant During Pregnancy
NCT05198245 · start 2021-12-15
Registered record
- Registry ID
- NCT05198245
- Conditions
- Migraine
- Interventions
- Rimegepant; Various; No intervention
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Active not recruiting
- Start
- 2021-12-15
- Completion
- 2028-04-30
- Enrolment
- 1
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMigraineInterventionRimegepant; Various; No interventionPhaseNot recordedRegistry statusActive not recruitingA Study of Galcanezumab (LY2951742) in Adult Participants With Episodic Migraine
NCT05127486 · start 2021-12-06
Registered record
- Registry ID
- NCT05127486
- Conditions
- Migraine; Episodic Migraine
- Interventions
- Galcanezumab; Rimegepant; Placebo; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2021-12-06
- Completion
- 2023-05-23
- Enrolment
- 580
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMigraine; Episodic MigraineInterventionGalcanezumab; Rimegepant; Placebo; PlaceboPhasePhase 4Registry statusCompletedObservational Study to Assess Maternal, Fetal and Infant Outcomes Following Exposure to Rimegepant
NCT05046613 · start 2021-09-23
Registered record
- Registry ID
- NCT05046613
- Conditions
- Migraine
- Interventions
- Rimegepant; Not taking Rimegepant
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Recruiting
- Start
- 2021-09-23
- Completion
- 2034-04-30
- Enrolment
- 780
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMigraineInterventionRimegepant; Not taking RimegepantPhaseNot recordedRegistry statusRecruitingAn Efficacy and Safety of Proprietary Formulations of Oral Ketamine + Aspirin in Treatment of Acute Headache
NCT04860713 · start 2021-04-22
Registered record
- Registry ID
- NCT04860713
- Conditions
- Pain
- Interventions
- aspirin and ketamine; Nurtec (Rimegepant)
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2021-04-22
- Completion
- 2022-11-17
- Enrolment
- 5
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPainInterventionaspirin and ketamine; Nurtec (Rimegepant)PhasePhase 4Registry statusCompletedRimegepant in Moderate Plaque-type Psoriasis
NCT04629950 · start 2021-01-19
Registered record
- Registry ID
- NCT04629950
- Conditions
- Psoriasis
- Interventions
- Rimegepant; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2021-01-19
- Completion
- 2024-11-18
- Enrolment
- 41
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPsoriasisInterventionRimegepant; PlaceboPhasePhase 2Registry statusCompletedRandomized Study in Children and Adolescents With Migraine: Acute Treatment
NCT04649242 · start 2021-01-15
Registered record
- Registry ID
- NCT04649242
- Conditions
- Pediatric Migraine
- Interventions
- Rimegepant/BHV3000; Matching placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Recruiting
- Start
- 2021-01-15
- Completion
- 2029-01-09
- Enrolment
- 2,100
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPediatric MigraineInterventionRimegepant/BHV3000; Matching placeboPhasePhase 3Registry statusRecruitingSafety and Efficacy Trial of BHV3000 (Rimegepant) 75 mg for the Acute Treatment of Migraine
NCT04574362 · start 2020-10-22
Registered record
- Registry ID
- NCT04574362
- Conditions
- Acute Migraine
- Interventions
- Rimegepant; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2020-10-22
- Completion
- 2021-12-16
- Enrolment
- 1,648
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAcute MigraineInterventionRimegepant; PlaceboPhasePhase 3Registry statusCompletedTrial for Treatment Refractory Trigeminal Neuralgia
NCT03941834 · start 2019-06-25
Registered record
- Registry ID
- NCT03941834
- Conditions
- Trigeminal Neuralgia
- Interventions
- Rimegepant; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Terminated
- Start
- 2019-06-25
- Completion
- 2023-05-11
- Enrolment
- 65
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionTrigeminal NeuralgiaInterventionRimegepant; PlaceboPhasePhase 2Registry statusTerminatedEfficacy and Safety Trial of Rimegepant for Migraine Prevention in Adults
NCT03732638 · start 2018-11-14
Registered record
- Registry ID
- NCT03732638
- Conditions
- Migraine
- Interventions
- Rimegepant; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 2 / Phase 3
- Registry status
- Completed
- Start
- 2018-11-14
- Completion
- 2021-02-02
- Enrolment
- 1,590
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMigraineInterventionRimegepant; PlaceboPhasePhase 2 / Phase 3Registry statusCompletedTrial in Adult Subjects With Acute Migraines
NCT03461757 · start 2018-02-27
Registered record
- Registry ID
- NCT03461757
- Conditions
- Migraine, With or Without Aura
- Interventions
- Rimegepant; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2018-02-27
- Completion
- 2018-10-15
- Enrolment
- 1,811
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMigraine, With or Without AuraInterventionRimegepant; PlaceboPhasePhase 3Registry statusCompleted