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Drug ReportsRimegepant
Nurtec odt, Vydura(rimegepant)
Nurtec, Vydura (rimegepant) is a small molecule pharmaceutical. Rimegepant was first approved as Nurtec odt on 2020-02-27. It is used to treat migraine disorders, migraine with aura, and migraine without aura in the USA. It has been approved in Europe to treat migraine disorders.
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FDA Novel Drug Approvals 2020
Events Timeline
Commercial
Clinical
Drug
Target
Variants
Financial
Trends
Safety
Events Timeline
5D
1M
3M
6M
YTD
1Y
2Y
5Y
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Events
FDA approval date
EMA approval date
Patent expiration date
Study first post date
Last update post date
Start date
Primary completion date
Completion date
Results first post date
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Commercial
Therapeutic Areas
Therapeutic Area
MeSH
nervous system diseasesD009422
Trade Name
FDA
EMA
Nurtec
Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
Rimegepant sulfate
Tradename
Company
Number
Date
Products
NURTEC ODTPfizerN-212728 RX2020-02-27
1 products, RLD, RS
Labels
FDA
EMA
Brand Name
Status
Last Update
nurtec odtNew Drug Application2024-04-12
Agency Specific
FDA
EMA
Expiration
Code
RIMEGEPANT SULFATE, NURTEC ODT, PFIZER
2025-02-27NCE
2024-05-27I-865
Patent Expiration
Patent
Expires
Flag
FDA Information
Rimegepant Sulfate, Nurtec Odt, Pfizer
110837242039-03-25DPU-2718, U-3142
87593722033-02-25DS, DP
83141172030-03-09DS, DPU-2718, U-3142
ATC Codes
N: Nervous system drugs
— N02: Analgesics
— N02C: Antimigraine preparations
— N02CD: Calcitonin gene-related peptide (cgrp) antagonists
— N02CD06: Rimegepant
HCPCS
No data
Clinical
Clinical Trials
45 clinical trials
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Indications Phases 4
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Migraine disordersD008881EFO_0003821G43131571438
HeadacheD006261HP_0002315R51—1—2—3
Migraine without auraD020326EFO_0005296G43.0———123
Migraine with auraD020325EFO_0005295G43.1———123
PainD010146EFO_0003843R52———1—1
PhotophobiaD020795HP_0000613H53.14———1—1
HyperacusisD012001—H93.23———1—1
Indications Phases 3
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
SinusitisD012852EFO_0007486J32——1——1
Nasal polypsD009298HP_0100582J33——1——1
PolypsD011127EFO_0000662———1——1
RhinosinusitisD000096825————1——1
Temporomandibular joint disordersD013705—M26.6——1——1
Temporomandibular joint dysfunction syndromeD013706————1——1
Premenstrual syndromeD011293—N94.3——1——1
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
PsoriasisD011565EFO_0000676L40—1———1
NeuralgiaD009437EFO_0009430——1———1
Trigeminal neuralgiaD014277EFO_1001219G50.0—1———1
Cluster headacheD003027HP_0012199G44.00—1———1
Irritable bowel syndromeD043183EFO_0000555K58—1———1
Indications Phases 1
No data
Indications Without Phase
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Overactive urinary bladderD053201EFO_1000781N32.81————11
Interstitial cystitisD018856EFO_1000869N30.1————11
SyndromeD013577——————11
CystitisD003556EFO_1000025N30————11
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameRimegepant
INNrimegepant
Description
Rimegepant, sold under the brand name Nurtec ODT among others, is a medication used for the acute treatment of migraine with or without aura in adults and the prophylactic/ preventive treatment of episodic migraine in adults. It is taken by mouth to dissolve on or under the tongue. It works by blocking CGRP receptors.
Classification
Small molecule
Drug classcalcitonin gene-related peptide receptor antagonists
Image (chem structure or protein)Loading
Structure (InChI/SMILES or Protein Sequence)
N[C@@H]1c2cccnc2[C@H](OC(=O)N2CCC(n3c(=O)[nH]c4ncccc43)CC2)CC[C@H]1c1cccc(F)c1F
Identifiers
PDB—
CAS-ID1289023-67-1
RxCUI—
ChEMBL IDCHEMBL2178422
ChEBI ID—
PubChem CID51049968
DrugBankDB12457
UNII ID997WVV895X (ChemIDplus, GSRS)
Target
No data
Variants
No data
Financial
Revenue by drug
$
€
£
â‚£
Vydura – Pfizer
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Estimated US medical usage
No data
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 455 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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7,294 adverse events reported
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