Amgen Halts study of Drug for Parkison's Disease GDNF
As part of that decision, and based on thorough scientific review, Amgen has also concluded that it will not provide GDNF to the 48 patients who participated in clinical trials that were terminated in the fall of 2004.
"We've looked at this decision from every perspective -- scientific, medical and ethical. Our hearts truly go out to trial patients and their families, but we simply cannot allow trials to continue given the potential safety risks and the absence of proven benefit," said Kevin Sharer, Amgen's chairman and chief executive officer. "Our desire is to actively pursue GDNF in a meaningful way that may benefit all Parkinson's disease patients."
"After careful review, we stand behind our decision to stop providing GDNF to patients due to potential safety risks observed in preclinical studies, including irreversible brain damage, and the absence of any demonstrated medical benefit," stated Roger M. Perlmutter, executive vice president, Research and Development, Amgen.
Amgen has actively studied Parkinson's disease therapies for more than a decade and will continue to support GDNF and the Parkinson's disease community by continuing to conduct additional research to better understand the potential of GDNF in the treatment of this terrible disease.
Discussions have been initiated with patient advocacy groups and research funding agencies to make Amgen's GDNF and other proprietary GDNF-related materials available to qualified pre-clinical researchers. Additionally, Amgen will pursue publication of both the Phase 2 study and toxicology data to further scientific understanding. Amgen will also expand the toxicology studies and work on discoveries to improve delivery of the drug.
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