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Onabotulinumtoxin A

Wake Forest University Health Sciences · FDA-approved active Small molecule ✓ Verified Jun 2026

Onabotulinumtoxin A is a Botulinum toxin Small molecule drug developed by Wake Forest University Health Sciences. It is currently FDA-approved for Cervical dystonia, Blepharospasm, Strabismus. Also known as: Botox, Botulinum toxin, Dysport, BOTOX.

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

Onabotulinumtoxin A is used to treat various conditions, including cutaneous leiomyomas, hereditary leiomyomatosis and renal cell cancer, interstitial cystitis, and cerebral palsy. It is administered through injections of botulinum toxin type A, which is a neurotoxin that blocks nerve signals.

At a glance

Generic nameOnabotulinumtoxin A
Also known asBotox, Botulinum toxin, Dysport, BOTOX, Botox ®, "Allergan"
SponsorWake Forest University Health Sciences
Drug classBotulinum toxin
TargetSNAP-25 (synaptosome-associated protein of 25 kDa)
ModalitySmall molecule
Therapeutic areaNeurology, Dermatology, Urology
PhaseFDA-approved

Mechanism of action

The drug is a botulinum toxin serotype A that irreversibly cleaves SNAP-25, a protein essential for acetylcholine vesicle fusion and release. This prevents neuromuscular transmission, leading to localized muscle weakness or paralysis that typically lasts 3-4 months. The effect is temporary because the body gradually regenerates new nerve terminals.

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

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Frequently asked questions about Onabotulinumtoxin A

What is Onabotulinumtoxin A?

Onabotulinumtoxin A is a Botulinum toxin drug developed by Wake Forest University Health Sciences, indicated for Cervical dystonia, Blepharospasm, Strabismus.

How does Onabotulinumtoxin A work?

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

What is Onabotulinumtoxin A used for?

Onabotulinumtoxin A is indicated for Cervical dystonia, Blepharospasm, Strabismus, Chronic migraine, Severe primary axillary hyperhidrosis.

Who makes Onabotulinumtoxin A?

Onabotulinumtoxin A is developed and marketed by Wake Forest University Health Sciences (see full Wake Forest University Health Sciences pipeline at /company/wake-forest-university-health-sciences).

Is Onabotulinumtoxin A also known as anything else?

Onabotulinumtoxin A is also known as Botox, Botulinum toxin, Dysport, BOTOX, Botox ®, "Allergan".

What drug class is Onabotulinumtoxin A in?

Onabotulinumtoxin A belongs to the Botulinum toxin class. See all Botulinum toxin drugs at /class/botulinum-toxin.

What development phase is Onabotulinumtoxin A in?

Onabotulinumtoxin A is FDA-approved (marketed).

What are the side effects of Onabotulinumtoxin A?

Common side effects of Onabotulinumtoxin A include Headache, Neck pain, Injection site pain, Muscle weakness, Eyelid ptosis, Dry mouth.

What does Onabotulinumtoxin A target?

Onabotulinumtoxin A targets SNAP-25 (synaptosome-associated protein of 25 kDa) and is a Botulinum toxin.

Related

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing