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Event Description

Learning Objectives

  • Learn what to include in a well-written protocol to ensure successful recruitment and data collection, as well as guidance for investigators and site staff new to immunotherapy trials.
  • Understand how to select measurable endpoints and when to consider pharmacodynamic (PD) endpoints for bioequivalence studies.
  • Gain an understanding of dosing and patient response challenges unique to immunotherapy trials, including dose-escalation, irRC versus RECIST, and pseudo disease progression.
  • Recognize the distinct challenges smaller companies face when embarking on immunotherapy studies.

If the Mastering Oncology Immunotherapy Clinical Trials: The Smaller Biopharmaceutical Perspective is important to your business, act now and make the appropriate connections. See the contact information below.

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Event Details

Conference/Event Dates: 05/05/2016 - 05/05/2016
Classification: B2B
Primary Industry: Oncology-Hematology
Other Industries: Cancer, Clinical Pharmacology, Oncology-Hematology, Professional Healthcare
Audience: This webinar is intended for oncology professionals who oversee immuno-oncology drug development and clinical research in North America and Europe. Attendees may include:

VPs/Directors of Clinical Operations / Outsourcing / Procurement / Project Management / Study Management
Immuno-oncology/Oncology division leaders
Data Managers
Medical Monitors
Medical Advisors

Booth Details

Booth Size Booth Cost   Available Amenities
No exhibiting.   Electricity: n/a
  Water: n/a
  Generator: n/a
  Marketing Vehicles Allowed: n/a
Other Booth Sizes Available: n/a

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Mastering Oncology Immunotherapy Clinical Trials: The Smaller Biopharmaceutical Perspective

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