Oncology Clinical Trial Endpoints - Keys to Maximizing Success in Your Development Programs
Mar 11 2013 11:00AM - Mar 11 2013 12:30PM | Online
This Solution Provider Webinar is brought to you by DIA in cooperation with ICON plc. Registration for Solution Provider Webinars are FREE! Sign up by clicking on the Register Online button.
The cost of drug development is high partly because of the high rates of failure. Understanding why some trials of promising products do not succeed makes it more likely that your next trial will avoid the pitfalls. This 90-minute webinar will provide you with strategies to improve your cancer development programs, as well as detailed discussions on how the implementation of better trial design & medical imaging data provide early indicators on future drug success.
Please Note: Continuing Education Credits are not available for this event.
- Why are oncology clinical trial success rates so low?
- Challenges and strategies to improve cancer drug development
- Medical Imaging in Oncology Trials: How do we get from images to endpoints?
Who Should Attend
Professionals who work in the area of:
- Clinical Operations
- Regulatory Affairs
- Medical Affairs
- Drug Safety & Pharmacovigilance
At the conclusion of this webinar, participants should be able to:
- Identify strategies to improve the cancer drug development process
- Improving early phase trial design to better predict phase III success
- Understand how medical imaging data is used to support oncology trial endpoints
- Discuss the use of advanced imaging methods for early determination of drug efficacy
Registration for Solution Provider Webinars are FREE! Sign up by clicking on the Register Online button.
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Unless otherwise disclosed, the statements made by speakers represent their own opinions and not necessarily those of the organization they represent, or that of the Drug Information Association. Speakers, agenda and CE information are subject to change without notice. Recording of any DIA educational material in any type of media is prohibited without prior written consent from DIA.