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Disease

Migraine, familial hemiplegic, 3

Late-stage therapeutic development

Also known as SCN1A familial or sporadic hemiplegic migraine, familial or sporadic hemiplegic migraine caused by mutation in SCN1A, migraine, familial hemiplegic, type 3, FHM3.

24
Clinical trials
1
Associated genes
1
Related proteins

What's happening now

An analyst briefing on current research, clinical, regulatory and industry activity surrounding this disease.

Clinical Milestones14View all 14
+6 more in the activity timeline below
Activity timeline14

Clinical trials

11 sponsors · 0 new · 5 completed in the last 12 months (net -2)

The current development programme across all trial phases.

Clinical programme
24
All trials
6
Active
18
Late-stage
6
Completed
Late-stage studies
Recruiting
Recently completed

Evidence coverage

8 treatments

How much of this condition's readable clinical evidence the confidence engine has incorporated, across its most-studied treatments. This measures coverage of the evidence base — not whether any treatment works.

High evidence coverage
88% · 29/33 eligible items incorporated

Largest gap: no meaningful change (2, trial-readability).

Associated genes

1 match

Genes associated with this disease in the canonical knowledge graph (Open Targets evidence). Number shows the association score.

Disease biology

1 match

Proteins whose encoding gene is associated with this disease, reached through the canonical gene→disease graph. Number shows the gene's association score.

Reference

Authoritative identity, definition & identifiers.

Synonyms

SCN1A familial or sporadic hemiplegic migraine, familial or sporadic hemiplegic migraine caused by mutation in SCN1A, migraine, familial hemiplegic, type 3, FHM3

References & data sources
  • Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
  • Clinical trials — ClinicalTrials.gov (U.S. National Library of Medicine)
  • Related entities are derived from literature co-mention (studied together) — associative, not causal.