Botox (onabotulinumtoxinA)

Company
Allergan

Approval Status
Approved March 2010

Treatment for
upper limb spasticity

Possible similar drugs
Botox; Botox Cosmetic

Areas
Musculoskeletal , Neurology & Nervous System

Botox for injection is a sterile, vacuum-dried purified botulinum toxin type A, produced from fermentation of Hall strain Clostridium botulinum type A. Botox blocks neuromuscular transmission by binding to acceptor sites on motor or sympathetic nerve terminals, entering the nerve terminals, and inhibiting the release of acetylcholine. Acetylcholine is a neurotransmitter in both the peripheral nervous system and central nervous system and causes the activation of muscle movement.

Among other indications, Botox has been approved specifically for upper limb spasticity in adult patients, to decrease the severity of increased muscle tone in elbow flexors, wrist flexors and finger flexors.

Botox is supplied as a vacuum-dried powder for reconstitution with sterile, non-preserved Sodium Chloride Injection. It is supplied as single-use 50 Unit and 100 Unit vials. Dosing of Botox for upper limb spasticity in initial and sequential treatment sessions should be tailored to the individual based on the size, number and location of muscles involved, severity of spasticity, the presence of local muscle weakness, the patient's response to previous treatment, or adverse event history with Botox. The recommended initial doses are as follows:
Biceps Brachii:100 - 200 Units divided in 4 sites
Flexor Carpi Radialis: 12.5 - 50 Units in 1 site
Flexor Carpi Ulnaris: 12.5 - 50 Units in 1 site
Flexor Digitorum Profundus: 30 - 50 Units in 1 site
Flexor Digitorum Sublimis: 30 - 50 Units in 1 site

FDA Approval
The efficacy and safety of Botox for the treatment of upper limb spasticity was evaluated in three randomized, multi-center, double-blind, placebo-controlled studies. Efficacy was measured according to the The Ashworth Scale, a clinical measure of the force required to move an extremity around a joint, with a reduction in score clinically representing a reduction in the force needed to move a joint. Possible scores range from 0 (no increase in muscle tone) to 4 (limb rigid in flexion or extension- very severe)

Study One
This trial enrolled 126 patients with upper limb spasticity who were at least 6 months post-stroke. Botox (a total dose of 200 Units to 240 Units) and placebo were injected intramuscularly into the flexor digitorum profundus, flexor digitorum sublimis, flexor carpi radialis, flexor carpi ulnaris, and if necessary into the adductor pollcis and flexor pollcis longus. The subjects were followed for 12 weeks. The primary efficacy variable was wrist flexors muscle tone at week 6. The median change from baseline was -2.0 for the Botox arm compared to 0.0 for the placebo arm (p≤0.05). The median change from baseline in muscle tone for Finger Flexor was -1.0 for the Botox arm and 0.0 for the placebo arm (p≤0.05). The median change from baseline for thumb flexor muscle tone was -1.0 for both arms.

Study Two
This study compared three doses of Botox (360 Units, 180 Units or 90 Units) with placebo in 91 patients with upper limb spasticity who were at least 6 weeks post-stroke. Botox and placebo were injected into the flexor digitorum profundus, flexor digitorum sublimis, flexor carpi radialis, flexor carpi ulnaris, and biceps brachii. The primary efficacy variable in Study 2 was the wrist flexor tone at Week 6. The median change from baseline was -1.5. -1.0. -1.5 for the three Botox arms (90, 180 and 360 Units) respectively and -1.0 for the placebo arm (p≤0.05). Key secondary endpoints including Physician Global Assessment, finger flexors muscle tone, and elbow flexors muscle tone were also reached.

Study Three
This study compared three doses of Botox (360, 180 or 90 Units) with placebo in 88 patients with upper limb spasticity at least 6 months post-stroke. The primary efficacy variable was wrist and elbow flexor tone. The median change from baseline on the wrist flexor muscle tone was -1.0, -1.0, -1.5 for Botox 90, 180 and 360 Units, respectively and -0.5 for placebo (p≤0.05 for Botox 360 Units vs. placebo). The median change from baseline for elbow flexor muscle tone was -0.5, -0.5 and -1.0 for the three Botox arms, respectively, and -0.5 for the placebo arm (p≤0.05 for Botox 360 Units vs. placebo). The key secondary endpoint, mean change in finger flexor tone, was also reached with statistical significance.

Adverse reactions associated with the use of Botox for upper limb spasticity may include, but are not limited to, the following:

  • pain in extremity
  • bronchitis
  • fatigue
  • nausea

Botox for injection is a sterile, vacuum-dried purified botulinum toxin type A, produced from fermentation of Hall strain Clostridium botulinum type A. Botox blocks neuromuscular transmission by binding to acceptor sites on motor or sympathetic nerve terminals, entering the nerve terminals, and inhibiting the release of acetylcholine. This inhibition occurs as the neurotoxin cleaves SNAP-25, a protein integral to the successful docking and release of acetylcholine from vesicles situated within nerve endings. When injected intramuscularly at therapeutic doses, Botox produces partial chemical denervation of the muscle resulting in a localized reduction in muscle activity. In addition, the muscle may atrophy, axonal sprouting may occur, and extrajunctional acetylcholine receptors may develop.

For additional information regarding Botox or upper limb spasticity, please visit the Botox web page.

Botox (onabotulinumtoxinA) Drug Information

The Botox (onabotulinumtoxinA) drug information shown above is licensed from Thomson CenterWatch. The information provided here is for general educational purposes only and does not constitute medical or pharmaceutical advice which should be sought from qualified medical and pharmaceutical advisers.

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