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| Measuring patient-reported tolerability in oncology trials | January 28: Join experts from University of Birmingham, Takeda, and Signant Health for a live online discussion about patient-reported tolerability assessment across oncology development phases. You'll learn why traditional adverse event reporting falls short, and how patient-centered tolerability assessment enhances dose-finding decisions and strengthens regulatory submissions. Plus, get practical frameworks for integrating PROs across oncology development phases. Get the details and save your spot today. |
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| Trends In Rare Disease Trials | Guest Column | By Sapna Rani and Monica Nandagopal, Beroe, Inc. | In the third article of this series, analyst reveal their top six recommendations for designing selection criteria and selecting solution options to optimize rare disease research outcomes. |
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| Why Feasibility Still Feels Broken | From The Editor | By Dan Schell, chief editor, Clinical Leader | Addressing feasibility requires more than process tweaks; it demands better communication, streamlined data collection, and collaborative planning to ensure sites are equipped to deliver. Access the full article to learn why feasibility still feels broken and explore practical strategies to improve accuracy, reduce burden, and strengthen site-sponsor relationships. |
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| Pioneering Strategies For Early-Phase Oncology Trials | Article | By Erin Finot and Matt Simmons, IQVIA Biotech | Adaptive methods and regulatory shifts are reshaping early-phase oncology trials, boosting efficiency, flexibility, and access so novel treatments reach patients faster and more effectively. |
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| You're receiving the Wednesday edition of the Clinical Leader newsletter, focusing on Decentralized Trials and Trial Management. To make changes to your newsletter selections, update your topic preferences. - Clinical Sites | Patient Centricity | Patient Recruitment (Monday)
- Clinical Trial Technology (Tuesday)
- Decentralized Trials | Trial Management (Wednesday)
- Outsourcing Models | Regulatory & Compliance (Thursday)
- Clinical Data Management & Analytics | Trial Monitoring (Friday)
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