Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/44730
Title: Clinical Study Report and Individual Participant Data Transparency for US Food and Drug Administration-Approved Anticancer Drugs: A Call for Systematic Data Availability
Authors: Modi, Natansh D.
Swain, Sandra M.
BUYSE, Marc 
Kuderer, Nicole M.
Rowland, Andrew
Rockhold, Frank W.
Sorich, Michael J.
Hopkins, Ashley M.
Issue Date: 2024
Publisher: LIPPINCOTT WILLIAMS & WILKINS
Source: Journal of clinical oncology, 42 (32) , p. 3773 -3777
Abstract: Unlocking the full potential of clinical trials through comprehensive CSR and IPD sharing can revolutionize cancer care, enhance safety evaluations, and reduce bias in systematic reviews. It is time for all stakeholders to embrace transparency and advance patient-centered outcomes.
Notes: Hopkins, AM (corresponding author), Flinders Univ S Australia, Coll Med & Publ Hlth, Adelaide, Australia.
ashley.hopkins@flinders.edu.au
Keywords: Humans;United States;Neoplasms;Clinical Trials as Topic;United States Food and Drug Administration;Antineoplastic Agents;Drug Approval
Document URI: http://hdl.handle.net/1942/44730
ISSN: 0732-183X
e-ISSN: 1527-7755
DOI: 10.1200/JCO.24.00539
ISI #: 001348825000018
Category: A2
Type: Journal Contribution
Appears in Collections:Research publications

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