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Pick up to three peptides to see how their mechanisms, studied uses and evidence levels differ. Rows where the entries disagree are marked with a blue edge.
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Comparison
Ziconotide
Cognitive & neuro
Evidence level
Moderate evidence
Approval status
Approved drug
Mechanism of action
- 1.Blocks N-type (Cav2.2) voltage-gated calcium channels on primary pain-sensing neurons.
- 2.Prevents calcium influx and the release of substance P and glutamate in the dorsal horn.
- 3.Reduces pain signalling without acting on opioid receptors.
- 4.Must be delivered into cerebrospinal fluid because it cannot cross the blood-brain barrier.
- 5.Has a narrow therapeutic window, with psychiatric and neurological effects close to the useful dose.
Studied for
- Severe chronic pain refractory to other treatment
- Neuropathic and cancer-related pain in intrathecal pump trials
- Opioid-refractory pain in patients already receiving intrathecal therapy
Reported effects
- Clinically meaningful pain reduction in a subset of patients in randomised trials
- No opioid tolerance or respiratory depression
- Neuropsychiatric effects such as confusion, hallucinations and mood change
- Requires slow titration over weeks
Side effects
- Dizziness and confusion
- Nausea and vomiting
- Nystagmus and abnormal gait
- Memory impairment
- Hallucinations and mood change
- Meningitis with pump complications
- Suicidal ideation reported
Research protocol
Research context only - an implanted intrathecal pump therapy managed by a pain specialist. Titration starts at 2.4 micrograms per day and increases slowly, with a maximum of 19.2 micrograms per day in most patients and no bolus dosing; trials measured pain intensity and adverse events over 3 to 6 weeks of titration.
Research context only
Evidence justification
Three randomised placebo-controlled intrathecal trials show analgesia in a subset of patients, but the narrow therapeutic index and small samples limit how strong that evidence can be.