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Thomas Knuijver

IrisZorg, Nijmegen, The Netherlands.

3 papers in the library · 65 citations · publishing 2016-2024

Papers

Safety of ibogaine administration in detoxification of opioid-dependent individuals: a descriptive open-label observational study.

Addiction (Abingdon, England) January 1, 2022 Thomas Knuijver, Arnt Schellekens, Maarten Belgers et al. 49 citations

A single dose of ibogaine (10 mg/kg) in 14 patients with opioid use disorder caused an average QTc prolongation of 95 ms (range 29–146 ms); half of the subjects reached a QTc over 500 ms. No life-threatening cardiac events occurred, but severe temporary ataxia (inability to walk without support) was universal. Withdrawal and psychomimetic effects were mostly manageable; 11 of 14 patients did not return to morphine within 24 hours. The findings indicate that ibogaine induces clinically relevant but reversible QTc prolongation, bradycardia, and severe cerebellar toxicity.

The pharmacokinetics and pharmacodynamics of ibogaine in opioid use disorder patients.

Journal of psychopharmacology (Oxford, England) May 1, 2024 Thomas Knuijver, Rob Ter Heine, Arnt F A Schellekens et al. 15 citations

Ibogaine, a hallucinogenic drug being studied for opioid use disorder, shows highly variable pharmacokinetics strongly linked to CYP2D6 genotype. In 14 patients given a single 10 mg/kg dose, ibogaine clearance increased by 30.7 L/h per point of CYP2D6 activity score, from a baseline of 0.82 L/h. Higher ibogaine plasma concentrations correlated significantly with QTc prolongation and cerebellar ataxia, while noribogaine did not. Neither ibogaine nor its metabolite correlated with opioid withdrawal severity. These findings suggest that cardiac and neurological side effects are driven more by ibogaine itself, and that lower or genotype-personalized dosing may improve safety.

Treatment of heroin dependence with ibogaine

European Psychiatry March 1, 2016 Arnt Schellekens, Toon van Oosteren, Thomas Knuijver et al. 1 citation

Ibogaine, a hallucinogen, reduces drug self-administration in animals, especially within the first 24 hours, but causes motor impairment and cerebral cell loss. In a meta-analysis of 27 animal studies, ibogaine did not affect conditioned place preference. Human data from 15 opiate-dependent patients treated with 10 mg/kg ibogaine are still being collected; initial observations show strong QTc prolongation and ataxia, with relatively mild opiate withdrawal symptoms. Ibogaine may reduce opiate withdrawal but carries risks of transient cardiac and cerebellar toxicity, warranting further systematic studies on its safety and efficacy for treating opiate dependence.