Access to Non-Summary Clinical Trial Data for Research Purposes Under EU Law

Author: Daria Kim
Publisher: Springer International
ISBN: 9783030867805
Published In: October 2022
Format: Paperback
Jurisdiction: Switzerland ? Disclaimer:
Countri(es) stated herein are used as reference only

RMB 1,286.56

Download Order Form

Add to Wishlist
| Add to Compare

Description
Contents

Details

This book draws a unique perspective on the regulation of access to clinical trial data as a case on research and knowledge externalities. Notwithstanding numerous potential benefits for medical research and public health, many jurisdictions have struggled to ensure access to clinical trial data, even at the level of the trial results. Pro-access policy initiatives have been strongly opposed by research-based drug companies arguing that mandatory data disclosure impedes their innovation incentives. Conventionally, access to test data has been approached from the perspective of transparency and research ethics. The book offers a complementary view and considers access to individual patient-level trial data for exploratory analysis as a matter of research and innovation policy. Such approach appears to be especially relevant in the data-driven economy where digital data constitutes a valuable economic resource. The study seeks to define how the rules of access to clinical trial data should be designed to reconcile the policy objectives of leveraging the research potential of data through secondary analysis, on the one hand, and protecting economic incentives of research-based drug companies, on the other hand. Overall, it is argued that the mainstream innovation-based justification for exclusive control over the outcomes of research and development can hardly rationalise trial sponsors' control over primary data from trials. Instead, access to such data and its robust analysis should be prioritised.

PART ONE: Setting the Scene

Introduction

The Context and the Problem in Focus

Secondary Analysis of Clinical Trial Data - A Primer

PART TWO: Analysis de lege lata

Legal Sources of Control over and Access to Clinical Trial Data under the EU Applicable Framework

Implications of IPD Disclosure for Statutory Innovation Incentives

PART THREE: Analysis de lege ferenda

Defining the Intervention Logic of Access-To-Data Measures - A Problem Analysis

Access to Clinical Trial Data as a Case on R&D Externalities - A Theoretical Framework

IPD as a Research Resource - Exclusively Controlled or Readily Accessible?

Evaluating Legislative Options