PainFDA Approved

Ziconotide (Prialt)

Intrathecal infusion

Overview

A synthetic 25-amino acid peptide identical to omega-conotoxin MVIIA, a neurotoxin found in the venom of the marine cone snail Conus magus. Ziconotide selectively and reversibly blocks N-type voltage-gated calcium channels (Cav2.2) in the dorsal horn of the spinal cord, inhibiting neurotransmitter release from primary afferent nociceptive neurons.

Mechanism of Action

It provides analgesia without opioid receptor activation, tolerance development, or respiratory depression..

Research Summary & Key Findings

FDA-approved in 2004 for severe chronic pain in patients refractory to or intolerant of systemic analgesics, adjunctive therapies, or intrathecal morphine. Requires intrathecal administration via implanted infusion pump. Clinical trials demonstrated significant pain reduction in patients with cancer pain and non-malignant pain syndromes. Narrow therapeutic index with dose-limiting neuropsychiatric side effects (cognitive impairment, hallucinations, psychosis) requires careful titration.

Clinical Status

FDA Approved

Ziconotide (Prialt) has received FDA approval and is available for clinical use under appropriate medical supervision. Consult a qualified healthcare provider for prescribing information.

Administration Routes

Intrathecal infusion

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Disclaimer: This information is provided for educational and research purposes only. It is not intended as medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider before starting any peptide therapy. The Peptide Association does not endorse or recommend any specific treatment protocol.