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Achieving Effective Hematological Oncology Clinical Trials

WEBINAR DETAILS

Date: November 3, 2015 (60 minutes)

Featured Speakers:

Hematology Oncology

This free webinar examines the nuances of successfully conducting hematological oncology clinical trials.

Hematological malignancies such as leukemia, multiple myeloma and lymphoma represent a subset of indications within oncology that are wholly different from solid tumors. The growing hematological oncology therapy market is fueling both large numbers of clinical studies and, more importantly, an enhanced and refined understanding of cancer pathologies. Conducting clinical trials in hematological malignancies requires an understanding of a rapidly evolving treatment paradigm that is increasingly nuanced, complex and patient-directed. Companies developing hematological oncology therapies must capitalize on the principles and infrastructures shared by solid tumor oncology trials while adapting endpoints, study designs and data management approaches as well as considering patients’ experiences to address the particular challenges related to investigating candidate treatments for blood-based cancers.

Join this webinar to gain an understanding of critical differences between solid tumor and hematological oncology and a discussion on the nuances of conducting successful hematological oncology clinical trials.

Learning Objectives

  • Understand critical trial design considerations; including tumor type, standard of care vs. research interests, and overall data capture nuances
  • Learn how to create meaningful, measurable endpoints and how they differ from solid tumor oncology studies
  • Recognize how to effectively monitor and manage data and queries within hematology oncology studies
  • Gain insight into selecting ideal trial sites for rare hematological malignancies and the importance of working with an oncology-experienced team

Keywords: Clinical Trials, Tumor Oncology, Hematology Oncology

    ABOUT OUR SPEAKERS

    Ray Reilly, Novella Clinical

    Ray Reilly, Senior Director, Oncology Division, Novella Clinical


    Ray Reilly has a combined 21 years in clinical research and is responsible for driving strategy and overseeing operations for Novella’s Oncology Division. He has managed many oncology programs and individual protocols including both early and late phase, domestic and international in scope. He possesses extensive knowledge of clinical research processes, project management methodology, regulations and guidelines. Ray’s experience spans site level work, academia, pharma and clinical research environments, with the last five years focused specifically on hematologic malignancies. During his ten year tenure with Novella, he has been involved in ensuring continued excellence within the company during significant corporate growth and has had involvement within clinical monitoring, regulatory/QA, clinical training and project management.

    Richard Gams, Novella Clinical

    Richard Gams, MD, Chief Scientific Officer, Novella Clinical


    Dr. Richard Gams is a board-certified hematologist/oncologist with more than 40 years’ clinical research experience. As Novella’s chief scientific officer, he guides training, protocol design, medical monitoring and pharmcovigilance, and is focused primarily on hematologic malignancies including leukemias, lymphomas, myelodysplasia and multiple myeloma. Prior to joining Novella, he played an instrumental role at Adria Laboratories (now part of Pfizer) in moving three breast cancer drugs and a therapy for acute myelogenous leukemia to FDA approval and commercialization in the 1990s, and later founded Prologue Research International, a contract research organization. Dr. Gams served as a Professor of Medicine in the Division of Hematology/Oncology at the University of Alabama at Birmingham and Chairman of the Lymphoma Committee of the Southeastern Cancer Study Group. Additionally, he was Professor of Medicine in Hematology/Oncology and Director, Developmental Therapeutics for the Comprehensive Cancer Center (CCC) at The Ohio State University.

    THIS PROGRAM IS INTENDED FOR

    This webinar is intended for hematology oncology professionals who oversee hematological drug development and clinical research in North America. Attendees may include:

    • VPs/Directors of Clinical Operations / Outsourcing / Procurement / Project Management / Study Management
    • Hematology Oncology Division Leaders
    • Data Managers
    • Medical Monitors
    • Medical Advisors
    OUR XTALKS PARTNER FOR THIS EVENT

     

    Novella Clinical, a Quintiles company, is a global, full-service clinical research organization (CRO) serving the unique needs of small to mid-sized oncology companies. Novella’s dedicated oncology division is comprised of more than 300 oncology clinical trial specialists across all functional areas. We have specific hematological oncology teams and processes to support hematological studies that include board-certified hematologists /oncologists on staff and a network of 1,220+ hematological oncology experienced CRAs. Nearly 30 percent of our oncology portfolio focuses specifically in hematological oncology and our experience includes AML, CML, multiple myeloma, myelodysplastic syndromes, NHL and many rare indications. Learn more at www.novellaclinical.com/oncology.

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