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Genetically-encoded Molecular Probes to Study G Protein-coupled Receptors
Published on: September 13, 2013
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Nonprofit foundations spur translational research.
Paola Zaratin1, Mario Alberto Battaglia1, Maria P Abbracchio2
1Italian Multiple Sclerosis Foundation, Genoa, Italy.
Trends in Pharmacological Sciences
|December 3, 2014
Summary
Drug development for neurodegenerative disorders faces significant clinical translation challenges. A collective-impact approach involving multiple stakeholders is proposed to accelerate new therapeutic discoveries for patients.
Area of Science:
- Pharmacological research
- Neurodegenerative disease therapeutics
- Drug discovery and development
Background:
- Numerous basic discoveries in pharmacology fail clinical translation annually.
- Neurodegenerative disorders, such as Alzheimer's and Parkinson's, lack effective disease-modifying treatments.
- The transition from laboratory findings to patient-ready drugs is a major hurdle in pharmaceutical research.
Purpose of the Study:
- To outline the current challenges in the clinical translation of pharmacological discoveries.
- To propose a novel 'collective-impact' multistakeholder strategy.
- To expedite the development of urgently needed drugs for neurodegenerative diseases.
Main Methods:
- Analysis of current drug development and clinical translation barriers.
- Conceptualization of a collaborative, multistakeholder framework.
- Literature review on successful and unsuccessful drug development initiatives.
Main Results:
- Identification of key bottlenecks hindering the translation of basic research into clinical therapies.
- A proposed model for a 'collective-impact' approach integrating diverse stakeholders.
- Highlighting the potential of collaborative efforts to overcome translational gaps.
Conclusions:
- The current drug development pipeline is inefficient, particularly for neurodegenerative diseases.
- A coordinated, multistakeholder 'collective-impact' model can significantly improve clinical translation rates.
- This approach offers a promising pathway to accelerate the delivery of novel therapies to patients suffering from neurodegenerative disorders.
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