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Part of the HDFCCC K12 Concept to Completion, Strategies for Successful Clinical Trials. Learning objectives for this seminar are:

  • Describe the difference between objectives vs endpoints
  • Identify basic biostatistical methods in therapeutic and nontherapeutic clinical oncology trials  
  • Explain different types of innovative clinical trial design (e.g., phase 0, biomarker-driven, and adaptive designs)
  • Discuss tips of the trade- accommodating a limited budget/sample size, the role of an interim analysis (futility, safety, efficacy), use of safety lead-ins
  • Summarize tips for reviewing clinical data and pitfalls to avoid 

Speakers:

  • Pamela Munster, MD, Professor, Department of Medicine (Hematology/Oncology), UCSF; Director, Early Phase Clinical Trials Unit, Co-leader of the Center for BRCA Research, and Co-Leader, Molecular Oncology Program, UCSF Helen Diller Family Comprehensive Cancer Center
  • Ann Lazar, PhD, MS, Professor, Preventative and Restorative Dental Science, UCSF School of Dentistry 

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