There is a pressing need to address the current major gaps in epilepsy treatment, in particular drug-resistant epilepsy, anti-epileptogenic therapies and comorbidities. A major concern in the development of new therapies is that current preclinical testing is not sufficiently predictive for clinical efficacy. Methodological limitations of current preclinical paradigms may partly account for this discrepancy. Here we propose and discuss a strategy for implementing a “Phase II” multicentre preclinical drug trial model based on clinical Phase II/III studies designed to generate more rigorous preclinical data for efficacy. The goal is to improve the evidence resulting from preclinical studies for investigational new drugs that have shown strong promise in initial preclinical “Phase I” studies. This should reduce the risk for expensive clinical studies in epilepsy and therefore increase the appeal for funders (industry and government) to invest in their clinical development.
Proposal for a "phase II" multicenter trial model for preclinical new antiepilepsy therapy development
SIMONATO, Michele
2013
Abstract
There is a pressing need to address the current major gaps in epilepsy treatment, in particular drug-resistant epilepsy, anti-epileptogenic therapies and comorbidities. A major concern in the development of new therapies is that current preclinical testing is not sufficiently predictive for clinical efficacy. Methodological limitations of current preclinical paradigms may partly account for this discrepancy. Here we propose and discuss a strategy for implementing a “Phase II” multicentre preclinical drug trial model based on clinical Phase II/III studies designed to generate more rigorous preclinical data for efficacy. The goal is to improve the evidence resulting from preclinical studies for investigational new drugs that have shown strong promise in initial preclinical “Phase I” studies. This should reduce the risk for expensive clinical studies in epilepsy and therefore increase the appeal for funders (industry and government) to invest in their clinical development.I documenti in SFERA sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.