Novel designs of early phase trials for cancer therapeutics. (2018)

• Record Type: Book
• Further Information: Note: Edited by Shivaani Kummar, Chris Takimoto.
• Editors: Kummar, Shivaani; Takimoto, Chris
• Contents: Front Cover; Novel Designs of Early Phase Trials for Cancer Therapeutics; Copyright Page; Dedication; Contents; List of Contributors; Preface; 1 Changing Landscape of Early Phase Clinical Trials: Beyond the Horizon; 1.1 Historical Perspective; 1.2 Current Trends; References; 2 Requirements for Filing an Investigational New Drug Application; 2.1 Exemptions to Filing an IND; 2.2 Types of IND Applications; 2.3 Regulatory and Administrative Components of an IND Application; 2.4 FDA IND Review; 2.5 IND Reporting Requirements; 2.5.1 Expedited Safety Reporting; 2.5.2 Annual Reporting 2.6 FDA Meetings2.7 IND Applications for Combination Therapies; 2.8 Applications for Companion Diagnostic Devices; 3 The Evolution of Phase I Trials, Past, Present, and Future: A Biostatistical Perspective; 3.1 Traditional Dose Finding: Toxicity-Based Designs; 3.1.1 Common Trial Designs for Toxicity-Based Dose Finding of Single Agents; 3.1.2 Toxicity-Based Dose-Finding Designs for Combinations; 3.1.3 Other Toxicity-Based Dose-Finding Designs; 3.1.4 (Re)defining Toxicity Endpoints; 3.2 Efficacy and Toxicity-Based Dose-Finding Designs; 3.3 Expansion Cohorts and Phase I/II Trials 3.4 Recent Trends in Phase I Trial Designs3.4.1 Breakthrough Therapy Designation and Its Impact on Trial Designs; 3.4.2 Statistical Challenges in Dose Finding Based in the Era of Immunotherapies and Targeted Agents; 3.5 Where Do We Go From Here: Recommendations for Optimal Early Phase Dose-Finding Trials; 3.5.1 Windows of Time for Evaluation of Toxicities; 3.5.2 Intrapatient Dose Escalation; 3.5.3 Delayed Clinical Responses, "Pseudo-Progression, " and Duration of Response; 3.5.4 Measures of Efficacy for Dose Finding: Clinical Versus Correlative Outcomes; 3.5.5 Sample Size and Cohort Selection 3.5.6 Using Expansion Cohorts to Recalibrate Dose3.5.7 Abandon the Terms "Phase I, II, and III"; 3.6 Summary; References; 4 Evolving Early Phase Trial Designs: A Regulatory Perspective; 4.1 Introduction; 4.2 FDA Expedited Programs for Expediting the Development and Review of Drugs for Serious or Life-Threatening Conditions; 4.2.1 Fast Track Development Program Designation; 4.2.2 Breakthrough Therapy Development Program Designation; 4.2.3 Priority Review Designation of a New Drug Application/Biologics License Application; 4.2.4 Accelerated Approval and Regular Approval 4.3 Multiarm Expansion Cohorts in Early Phase Trials4.3.1 Traditional Drug Development Paradigm and Seamless Oncology Expansion Cohort Drug Development Paradigm; 4.3.2 Examples of Expansion Cohorts in Seamless Oncology Trials; 4.3.3 Regulatory Considerations of Seamless Oncology Expansion Cohort FIH Trials-Opportunities and Challenges; 4.3.3.1 Safety Considerations; 4.3.3.2 Efficacy Considerations; 4.4 Summary; References; 5 The Challenges of Implementing Multiarmed Early Phase Oncology Clinical Trials; 5.1 Introduction; 5.2 Evolution of Early Phase Clinical Trials; 5.2.1 Endpoints
• Publisher Details: London, United Kingdom : Academic Press, an imprint of Elsevier
• Publication Date: 2018
• Extent: 1 online resource
• Subjects: 615.7/98; Antineoplastic agents -- Testing; Drug development; MEDICAL / Pharmacology; Electronic books
• Languages: English
• ISBNs: 9780128125700; 0128125705
• Related ISBNs: 9780128125120; 0128125128
• Notes: Note: Online resource; title from PDF title page (ScienceDirect, viewed May 30, 2018).
• Access Rights: Legal Deposit; Only available on premises controlled by the deposit library and to one user at any one time; The Legal Deposit Libraries (Non-Print Works) Regulations (UK).
• Access Usage: Restricted: Printing from this resource is governed by The Legal Deposit Libraries (Non-Print Works) Regulations (UK) and UK copyright law currently in force.