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Drug

Erenumab

Approved medicine
ClassCalcitonin gene-related peptide type 1 receptor antagonistResearchOngoing clinical research

Also known as Aimovig.

1
Active clinical trials
CALCRL
Primary target
1
Regulatory events
Latest activity
beta

Recent clinical, regulatory, research and industry developments relating to this drug.

Hypersensitivity to CGRP as a Predictive Biomarker of Migraine Prevention With Erenumab

Clinical trial2025-08-01Primary completion · ClinicalTrials.gov

Approval: Aimovig (EMA)

Regulatory2018-07-26EMA

Profile

Identifiers & mechanism

Canonical identifiers, marketed brand names and mechanism, resolved across RxNorm, ChEMBL and ATC.

Canonical name
Erenumab
Aliases & brands
Aimovig
RxNorm CUI
2045613
ChEMBL ID
CHEMBL3833329
ATC codes
N02CD01
UNII
I5I8VB78VT
Primary mechanism
Calcitonin gene-related peptide type 1 receptor antagonist
Regulatory jurisdictions
ema

Pharmacology & targets

1 target

Known molecular targets and mechanisms supported by curated pharmacology databases.

ANTAGONISTCalcitonin gene-related peptide type 1 receptor antagonist

Regulatory timeline

1 event

The complete regulatory record, grouped by authority — approvals, safety advisories and label changes. Each authority shows its most recent events; expand one to read its full history.

Earliest approval
2018-07-26
Latest approval
2018-07-26
Authorities
EMA
Total events
1
emaEuropean Medicines Agency· 1 event
2018-07-26Approval
Approval: Aimovig (EMA)

Indication: Aimovig is indicated for prophylaxis of migraine in adults who have at least 4 migraine days per month when initiating treatment with Aimovig.

Evidence ↗

Contains information from the European Medicines Agency (European Medicines Agency), © EMA, reused under CC BY 4.0.

Clinical trials

39 trials

The current development programme across all trial phases — status mix, phase distribution and the late-stage studies shaping the evidence base.

Development programme
CLINICALTRIALS.GOV · LIVE REGISTRY
39
registered trials across all phases
LATEST COMPLETION 2024
1
Active studies
1
Recruiting
22
Late-stage (III+)
28
Completed
10
Discontinued
PHASE DISTRIBUTIONn = 39
Phase 18Phase 29Phase 36Phase 415Phase N / A1

Late-stage studies

Phase III+ trials still open or recently active — where late-stage evidence is being generated.

Recent completions

Trials that read out recently, adding to the completed evidence base.

References & data sources
  • RxNorm (U.S. National Library of Medicine) — drug identity
  • ChEMBL (EMBL-EBI) & UniProt — pharmacology and targets
  • ClinicalTrials.gov — clinical trials
  • Regulatory event sources are credited in the Regulatory Timeline above.