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Abstract
OBJECTIVE: To develop and implement an evidence based framework to select, from drugs already licenced, candidate oral neuroprotective drugs to be tested in secondary progressive multiple sclerosis.
DESIGN: Systematic review of clinical studies of oral putative neuroprotective therapies in MS and four other neurodegenerative diseases with shared pathological features, followed by systematic review and meta-analyses of the in vivo experimental data for those interventions. We presented summary data to an international multi-disciplinary committee, which assessed each drug in turn using pre-specified criteria including consideration of mechanism of action.
RESULTS: We identified a short list of fifty-two candidate interventions. After review of all clinical and pre-clinical evidence we identified ibudilast, riluzole, amiloride, pirfenidone, fluoxetine, oxcarbazepine, and the polyunsaturated fatty-acid class (Linoleic Acid, Lipoic acid; Omega-3 fatty acid, Max EPA oil) as lead candidates for clinical evaluation.
CONCLUSIONS: We demonstrate a standardised and systematic approach to candidate identification for drug rescue and repurposing trials that can be applied widely to neurodegenerative disorders.
Original language | English |
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Article number | e0117705 |
Journal | PLoS ONE |
Volume | 10 |
Issue number | 4 |
DOIs | |
Publication status | Published - 9 Apr 2015 |
Keywords / Materials (for Non-textual outputs)
- DOUBLE-BLIND
- ANIMAL-MODELS
- FLUOXETINE
- IBUDILAST
- THERAPY
- DISEASE
- QUALITY
- DESIGN
- TRIAL
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