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Advancing the Science of Patient Input in Drug Research and Development
Marilyn A Metcalf1, Henrietta Awo Osei-Anto2, Thomas J Sharpe3
1GSK, Durham, NC, United States.
Integrating patient input into drug research and development (R&D) creates better medicines. Addressing barriers to collecting and using patient data is key to advancing patient-centered drug discovery and improving health outcomes.
Area of Science:
- Patient-centered drug discovery and development
- Translational science
- Regulatory science
Background:
- Patient input is crucial for developing medicines that meet patient needs.
- Barriers hinder the systematic collection and use of patient data in drug R&D.
- Advancing the Science of Patient Input Action Collaborative addresses these implementation challenges.
Purpose of the Study:
- Identify and address key barriers to implementing patient input in drug R&D.
- Align drug discovery, development, and regulation with patient priorities.
- Promote practical paths for integrating patient perspectives into medical research and practice.
Main Methods:
- Multi-stakeholder engagement to gather diverse perspectives.
- Focus on three research priorities: patient experience, benefit-risk perspectives, and clinical trial integration.
- Leveraging existing guidances, strategies, and use-case lessons learned.
Main Results:
- Identified key barriers to the systematic integration of patient input.
- Defined research priorities to advance the science of patient input.
- Proposed a comprehensive framework for incorporating patient input throughout drug R&D.
Conclusions:
- Systematic patient input integration shifts R&D from ad-hoc applications to everyday practice.
- A comprehensive framework is essential for reimagining and enriching patient input in drug R&D.
- Enhanced patient input leads to medicines that better meet patient needs and improve disease management.
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