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Botulinum Toxin Type A 900kDa

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 900kDa
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 kDa form includes associated proteins that stabilize the toxin complex.

Approved indications

Common side effects

Key clinical trials

Primary sources

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