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The United States stands to benefit from tolperisone,

a treatment that has already helped increase the quality of life for millions in parts of Europe and Asia. 

TOLPERISONE  ADVANTAGE

Tolperisone Key Differentiators Compared to Cyclobenzaprine

Tolperisone is a medicine widely prescribed outside of the U.S. for acute muscle spasms and spasticity.  In the U.S., tolperisone is being investigated as a novel, non-opioid, non-sedating, non-drowsy muscle relaxant for the relief of pain due to muscle spasm. Tolperisone is predicted to have effective analgesic activity in addition to muscle relaxation because of its centrally-acting dual voltage gated calcium and sodium channel blocker mechanism of action.  

 

Neurana has completed a Phase 1 clinical study which confirmed the non-sedative properties of tolperisone using a driving simulation study.  Currently, Neurana is preparing to commence a Phase 2 dose-ranging clinical study, the “STAR Study”, to further demonstrate the safety and efficacy of tolperisone in subjects with acute, painful muscle spasms of the back.  Top line data from the Phase 2 “STAR” Study is anticipated in Q3 2019.

 

Composition of matter and process patents have been issued by the US Patent and Trademark Office (USPTO) providing Orange Book listable patent protection through 2032.

 
 

TOLPERISONE

CYCLOBENZAPRINE

Specific Pharmacology

Non Sedating

Broad Nervous System Coverage

Analgesic Effect

NON-SEDATION ADVANTAGE

Tolperisone is similar to placebo on Standard Deviation of Lateral Position (SDLP)

CREATE A POPOUT THAT COVERS THE RIGHT HAND SIDE WITH PPT DECK GRAPHIC

TOLPERISONE

 

UNIQUE

MECHANISM

OF ACTION

Inhibition of spinal reflexes via presynaptic blockade of both voltage-gated calcium channels and voltage-gated sodium channels

 

Reversible blockade of voltage-gated sodium and calcium channels

 

Dual mechanism of sodium and calcium channel blockade provides effective analgesic activity in addition to muscle relaxation

 

No binding activity directed to the benzodiazepine receptor

 

No opioid binding activity; no abuse potential