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Recruiting Phase 2 NCT06751784

Cross-over Study on the Influence of Fampridine on Working Memory in Mild to Moderate Depression

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Trial Parameters

Condition Working Memory
Sponsor University of Basel
Study Type INTERVENTIONAL
Phase Phase 2
Enrollment 38
Sex ALL
Min Age 18 Years
Max Age 55 Years
Start Date 2025-05-22
Completion 2026-07
Interventions
Fampridine SRPlacebo

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Brief Summary

Cognitive deficits, including working memory deficits, are often present in depression and there are currently no effective pharmacological treatments targeting working memory deficits. Papassotiropoulos et al. (2024) has recently demonstrated that fampridine, a potassium channel blocker, can enhance working memory in healthy individuals with lower baseline performance, suggesting it may hold potential for addressing cognitive deficits in clinical populations. The primary aim of this study is to evaluate whether fampridine improves working memory performance in mild to moderate depression

Eligibility Criteria

Inclusion Criteria: * Male or female * Major depressive episode confirmed by the Mini-DIPS. Currently mild to moderate (MADRS: 7-30). * Normotensive (BP: 90/60mmHg - 140/90mmHg). Sufficiently treated hypertensive subjects will be included. * BMI: 19 - 34,9 kg/m2 * Age: 18 - 55 years * Fluent in German * IC as documented by signature Exclusion Criteria: * Contraindications to the class of drugs under study, e.g. known hypersensitivity or allergy to 4-aminopyridine * Use of potassium channel blockers within the last 3 months * Treatment with OCT 2 inhibitors and -substrates (e.g. cimetidine, propranolol) * Treatment with antidepressants or antipsychotics within the last 3 months and throughout the study period * Current intake of psychoactive drugs (e.g. benzodiazepines, antidepressants, neuroleptics). * Other acute or chronic psychiatric disorder (e.g. psychosis, somatoform disorder, alcohol or drug abuse disorder) * Cognitive impairment (MoCA score \< 25) * MADRS item 10 \> 1 (suicidal

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