Last reviewed · How we verify

Botulinum Toxin Type A 900kD

Allergan · FDA-approved active Biologic

Botulinum toxin type A blocks acetylcholine release at the neuromuscular junction by cleaving SNARE proteins, causing temporary muscle paralysis.

Botulinum toxin type A blocks acetylcholine release at the neuromuscular junction by cleaving SNARE proteins, causing temporary muscle paralysis. Used for Cervical dystonia, Blepharospasm, Strabismus.

At a glance

Generic nameBotulinum Toxin Type A 900kD
Also known asBOTOX®
SponsorAllergan
Drug classNeurotoxin; acetylcholine release inhibitor
TargetSNAP-25 (synaptosome-associated protein of 25 kDa)
ModalityBiologic
Therapeutic areaNeurology; Aesthetics; Ophthalmology
PhaseFDA-approved

Mechanism of action

The toxin is a zinc-dependent endopeptidase that cleaves SNAP-25 (synaptosome-associated protein of 25 kDa), preventing acetylcholine vesicles from fusing with the presynaptic membrane. This results in flaccid paralysis of the injected muscle that typically lasts 3-4 months. The 900 kD formulation refers to the molecular weight of the toxin-protein complex, which includes associated proteins that may influence potency and duration.

Approved indications

Common side effects

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

Competitive intelligence

For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape: