PPT-End-Points and Rationale for Phase III Trials in HCC: Adjuvant, Intermediate, and Advanced

Author : maniakti | Published Date : 2020-08-28

Richard S Finn MD Professor of Clinical Medicine Division of Hematology Oncology Director Signal Transduction and Therapeutics Program Jonsson Comprehensive Cancer

Presentation Embed Code

Download Presentation

Download Presentation The PPT/PDF document "End-Points and Rationale for Phase III T..." is the property of its rightful owner. Permission is granted to download and print the materials on this website for personal, non-commercial use only, and to display it on your personal computer provided you do not modify the materials and that you retain all copyright notices contained in the materials. By downloading content from our website, you accept the terms of this agreement.

End-Points and Rationale for Phase III Trials in HCC: Adjuvant, Intermediate, and Advanced: Transcript


Richard S Finn MD Professor of Clinical Medicine Division of Hematology Oncology Director Signal Transduction and Therapeutics Program Jonsson Comprehensive Cancer Center at UCLA Geffen School of Medicine at UCLA. brPage 1br Basic Intermediate Advanced CONCOMITANT MEDICATIONS Has the patient taken any concomitant medications up until day X If yes please describe below No Yes Medication Generic Trad Module 3: Overview of Prevention Research. www.icad-cisd.com. UNDERSTANDING THE RESEARCH PROCESS. Clinical Trials Process. Preclinical. Phase I. Phase II. Phase IIB. “Test of Concept”. Phase III. OnCology. drug development. Jan 22, 2015. Methods in Clinical Cancer Research. Expansion Cohorts. What is an expansion cohort? Generally, a cohort of patients enrolled at the MTD or RP2D after it is defined based on a small number of patients at the dose. Acknowledgements to collaborators:. Stevely. A, Todd S, . Julious. S, Nicholl J, Hind D, and Cooper C. . #ICTMC2015. 1. Investigation of the shortcomings of the CONSORT 2010 statement for the reporting of group sequential randomised controlled trials. An investigation arising out of the Assignment 2012-2013. CS32310 – Nov 2013. H Holstein. 1. Abstract. Transformations of the coordinates defining points in a 3D scene can be carried out using vector formulae or matrix formulae. Challenging Tradition. Chia-Chi (Josh) Lin, MD, PhD . 林家齊. Director of Phase I Center, Department of Oncology, National Taiwan University Hospital. Clinical Associate Professor, Graduate Institute of Oncology, National Taiwan University College of Medicine. Yeh-Fong Chen, Ph.D. . FDA/CDER/OB/DB3. CBA 2016-2017 Workshop series-3 . Dec. 18, 2016. Disclaimer. This presentation reflects the views of . the author . and should not be construed to represent the views or policies of the U.S. Food and Drug Administration.. Andrew X. Zhu, MD, PhD. Harvard Medical School. Massachusetts General Hospital. Cancer Center. Jiahui. International Cancer Center. Disclosure . Advisory/consulting: Eisai, Bristol-Myers Squibb, Merck, Novartis, Astra-Zeneca, Bayer, Lilly, . GymnasticsCoach Mary Shannon CooperAugustDateClassTimeWednesday August 42021Beginner/IntermediateIntermediateCheer TumblingAdvanced330 415415 500500 545545 630Wednesday August 11 2021Beginner/Intermed Ashley E. Ross MD PhD. Executive Medical Director. Mary Crowley Cancer Research Centers. NASPCC Annual Meeting 2019. Objectives. Define GCP (Good Clinical Practice) and its applications for patients and research.. Professor Julia . Brown. Leeds Institute of Clinical Trials Research, University of Leeds. Introduction. First clinical trial in 1747, James Lind. Clinical trials are gold standard for the evaluation of new treatments/interventions in health care . Marina Di Marco. Principal Neuromuscular Physiotherapist. The changing landscape of research in DMD. Emily Crossley and Alex Johnson (co-founders of Duchenne UK and parents of children with DMD) were disappointed that clinical trials were being turned down in the UK because of lack of capacity.. Research. Outline. Is research for me?. Share some of my experiences. Project develop process and pitfalls. Phase . I/II trials. Delivering new agents. Supporting . trials. How to . S. etting up research team and program. Alison . Morris . | . Beatriz . Sanz-Bernardo | . Alison . Burman | . Anna . Ludi. The Pirbright Institute, Ash Road, Pirbright, Woking, GU24 0NF UK. Tel: +44 (0)1483 234455. . Email. : beatriz.sanz-bernardo@pirbright.ac.uk .

Download Document

Here is the link to download the presentation.
"End-Points and Rationale for Phase III Trials in HCC: Adjuvant, Intermediate, and Advanced"The content belongs to its owner. You may download and print it for personal use, without modification, and keep all copyright notices. By downloading, you agree to these terms.

Related Documents