Botulinum Toxin Type E

DB19082ApprovedProtein Based Therapies

Botulinum Toxin Type E is a botulinum neurotoxin serotype E indicated for temporary improvement of moderate to severe glabellar lines in adults, producing rapid-onset, short-duration chemical denervation through SNAP-25 cleavage. It blocks neuromuscular transmission by cleaving SNAP-25, producing partial chemical denervation and a localized reduction in muscle activity.

Mechanism
Curator reviewed · 5 references
Primary indication
TrenibotulinumtoxinE is indicated for the temporary improvement in the appearance of moderate to severe lines between the eyebrows seen at maximum frown (glabellar lines), when these have an important psychological impact, in adult patients.Curator reviewed · 1 structured indication
First approval
Canada, 2026
Also known as
BONTOXILYSIN-E · Botulinum neurotoxin serotype E · BOTULINUM NEUROTOXIN SEROTYPE E (BONT/E) (EB-001) · BOTULINUM NEUROTOXIN TYPE E
Code names
EB-001

Resolves to

Clinical / RWD

What you can answer from here — as of September 14, 2026

1Protein targetEach mapped to UniProt, with action and pharmacological action
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235Drug interactionsStructured to mechanism, not free text
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4Clinical trialsPhase, status and sponsor resolved per trial
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1Structured indicationCondition, population, route and combination as fields, not prose
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6ContraindicationsEach with its own population and attribute set
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1Marketed productAcross 1 country and 1 labeller
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1ATC codeIncluding every combination product, plus 29 drug categories
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6+ReferencesStructured and connected to the statements they support
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Which drugs share a target with Botulinum Toxin Type E, and which of those have an active Phase 3 trial?

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