Oncology drugs and added benefit: insights from 3 European health technology assessment agencies on the role of efficacy endpoints
Author:
Affiliation:
1. Maple Health Group, LLC, New York, NY, USA
2. EMD Serono Research & Development Institute, Inc, Billerica, MA, USA (an affiliate of Merck KGaA)
3. EMD Serono Research & Development Institute, Inc, Rockland, MA, USA (an affiliate of Merck KGaA)
Publisher
Informa UK Limited
Subject
Health Policy
Link
https://www.tandfonline.com/doi/pdf/10.1080/13696998.2021.2009711
Reference22 articles.
1. Surrogate endpoints in oncology: when are they acceptable for regulatory and clinical decisions, and are they currently overused?
2. Selection of Endpoints in Clinical Trials: Trends in European Marketing Authorization Practice in Oncological Indications
3. Health Technology Assessment Challenges in Oncology: 20 Years of Value in Health
4. The Difference Between Regulatory And Market Access Decisions On Treatment Availability For New Drugs In Six Common Cancers Across Australia, Canada, And Europe
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