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  1. pharmadog
  2. ›drugs
  3. ›Nurtec
drug · small molecule
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rimegepant sulfate ODT

Marketedupdated 5mo ago
by $PFE PFIZER INC🔗 ChEMBL
Approved
community read0 votes

🐶 often sniffed alongside

top 3
  • drugNURTEC ODT40 co-mentions · 10 sources
  • tagApproval40 co-mentions · 10 sources
  • tagSmall Molecule20 co-mentions · 10 sources

Small molecule drug with a maximum clinical stage of Approval, with an approval for migraine disorder.

targets

Calcitonin gene-related peptide type 1 receptor

all catalysts(10)

approval · 10
Feb 27, 2020
approval
$PFE27.80-1.14%
7y ago
NURTEC ODT (RIMEGEPANT SULFATE) — FDA approval
rimegepant sulfate ODT
→
Aug 18, 2020
approval
$PFE27.80-1.14%
6y ago
NURTEC ODT (RIMEGEPANT SULFATE) — FDA approval
rimegepant sulfate ODT
→
May 27, 2021
approval
$PFE27.80-1.14%
5y ago
NURTEC ODT (RIMEGEPANT SULFATE) — FDA approval
rimegepant sulfate ODT
→
Dec 8, 2021
approval
$PFE27.80-1.14%
5y ago
NURTEC ODT (RIMEGEPANT SULFATE) — FDA approval
rimegepant sulfate ODT
→
Mar 31, 2022
approval
$PFE27.80-1.14%
5y ago
NURTEC ODT (RIMEGEPANT SULFATE) — FDA approval
rimegepant sulfate ODT
→
Apr 11, 2022
approval
$PFE27.80-1.14%
4y ago
NURTEC ODT (RIMEGEPANT SULFATE) — FDA approval
rimegepant sulfate ODT
→
Dec 12, 2024
approval
$PFE27.80-1.14%
2y ago
NURTEC ODT (RIMEGEPANT SULFATE) — FDA approval
rimegepant sulfate ODT
→
Mar 21, 2025
approval
$PFE27.80-1.14%
2y ago
NURTEC ODT (RIMEGEPANT SULFATE) — FDA approval
rimegepant sulfate ODT
→
Aug 1, 2025
approval
$PFE27.80-1.14%
1y ago
NURTEC ODT (RIMEGEPANT SULFATE) — FDA approval
rimegepant sulfate ODT
→
Mar 16, 2026
approval
$PFE27.80-1.14%
7mo ago
NURTEC ODT (RIMEGEPANT SULFATE) — FDA approval
rimegepant sulfate ODT
→
view all 10 catalysts →

Trials studying rimegepant sulfate ODT

  • —A Study to Learn About the Study Medicine NURTEC® ODT 75 mg After it is Released Into the Markets in Koreanot yet recruitingn=3,000
  • phase2Comparison of Rimegepant and Placebo for Pain in IBScompletedn=24

Patent cliff

source: FDA Orange Book
first barrier falls
Feb 25, 2033
~6.4 years out

Earliest of all listed patents + FDA exclusivities. Generic / biosimilar entry typically only becomes possible AFTER both patent and exclusivity barriers expire.

patents (3)

  • Mar 25, 2039formulationUS 11083724
  • Feb 27, 2034compositionUS 8314117
  • Feb 25, 2033compositionUS 8759372

News(2)

  • New guidelines on migraine prevention reflect increasing options for patients
    “There has been a wealth of new treatment available” for migraine prevention, said a co-author of new guidelines released Monday.
    stat · 1mo ago
  • Biohaven trades cash for ‘upside’ with $795M epilepsy drug deal
    Faced with a dwindling bank account after a series of research setbacks, Biohaven is letting go of its most advanced experimental drug in a deal one analyst viewed as a “surprising” transaction.
    biopharma_dive · 1mo ago
brand
Nurtec
trade names
Nurtec odt, Vydura
generic
rimegepant sulfate
MOA
Calcitonin gene-related peptide type 1 receptor antagonist
indication
Rhinosinusitis
phase
marketed
Data sources
openFDA · ClinicalTrials.gov · OpenTargets
last refreshed 3h ago
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