Ziconotide
moderate riskAlso: Prialt · SNX-111 · Conotoxin MVIIA
Ziconotide (Prialt) is an FDA-approved omega-conotoxin peptide derived from cone snail venom for severe chronic pain requiring intrathecal delivery. It is the only approved non-opioid intrathecal analgesic. Blocks N-type voltage-gated calcium channels in the spinal cord dorsal horn.
Reported Benefits
Severe chronic pain
FDA-approved; Phase III trials demonstrate significant pain reduction vs. placebo in refractory pain states.
Mechanism of Action
Selective blocker of N-type (Cav2.2) voltage-gated calcium channels; inhibits nociceptive neurotransmitter release in spinal cord dorsal horn without opioid receptor involvement.
Key Clinical Studies
Staats et al. (2004)
Phase III RCT · n=220
Significant pain reduction vs. placebo in refractory pain; FDA approved 2004
Conotoxin: Cone Snail Venom Origin
Ziconotide is derived from Conus magus, a predatory marine cone snail. Cone snail venoms are a rich source of novel channel-blocking peptides. Ziconotide’s approval validates the cone snail venom class as a drug source.
Narrow Therapeutic Index
The dose-response curve is steep and side effects at higher doses are significant (psychiatric effects, cognitive impairment). Slow titration is mandatory. This limits its clinical use to experienced pain management specialists.
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Regulatory Status
FDA ApprovedFDA approved as Prialt (intrathecal use only)
Safety Profile
Side Effects
- •Dizziness
- •Nausea
- •Confusion
- •Psychiatric effects
- •Meningitis (catheter-related)
- •Narrow therapeutic index
Contraindications
- •Infection at pump site
- •Psychosis/depression history
- •Intrathecal opioids (safety uncertain)
Drug Interactions
- •Opioids (caution)
- •Antiepileptics
Primary Uses
Related Peptides
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