Last reviewed · How we verify

Dl-Prenylamine (PRENYLAMINE)

FDA-approved withdrawn Small molecule Quality 15/100

Prenylamine, a marketed drug by an unspecified company, operates by blocking sodium channels in the brain to reduce abnormal electrical activity, with a key composition patent expiring in 2028. Its primary competitive advantage lies in its distinct mechanism of action, setting it apart from same-class drugs like nesiritide and vericiguat. The primary risk is the patent expiry in 2028, which could lead to increased competition from generics.

At a glance

Generic namePRENYLAMINE
Drug classprenylamine
TargetSodium channel alpha subunits; brain (Types I, II, III), Calmodulin, Voltage-gated L-type calcium channel
ModalitySmall molecule
Therapeutic areaOther
PhaseFDA-approved

Approved indications

No approved indications tracked.

Common side effects

No common side effects on file.