Drug intelligence / Profile preview

daxibotulinumtoxinA

Development stage
Approved
Lead developer
Revance
Modality
Recombinant Proteins and Enzymes
Administration
Subcutaneous
01

Overview

DaxibotulinumtoxinA (DAXXIFY) is a long-acting botulinum toxin type A neuromodulator developed by Revance Therapeutics. It is the first botulinum toxin formulated with a proprietary 35-amino acid stabilizing peptide (RTP004) and without human serum albumin or animal-derived components. The drug's mechanism of action involves the proteolytic cleavage of SNAP-25, a protein essential for the docking and fusion of acetylcholine-containing vesicles with the presynaptic membrane at the neuromuscular junction. This inhibition of acetylcholine release results in temporary muscle relaxation. While FDA-approved for the treatment of glabellar lines and cervical dystonia, it is currently being investigated by Ki Health Partners LLC for the preventive treatment of high-frequency and chronic migraine using a novel subcutaneous injection paradigm (the "EEG paradigm") at a 310U dose.

Brand names
DAXXIFY
Other names
daxibotulinumtoxinA-lanm
02

Targets

SNAP25 (Synaptosome-associated protein 25)SV2A (Synaptic vesicle glycoprotein 2A)

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