Overview of NANT Clinical Trials - Part 1

This webinar was recorded on February 16,2010 

 

An Update on New Approaches to NeuroblastomaTherapy (NANT) Clinical Trials from Neuroblastoma Foundation on Vimeo.

 

Space is limited.
Reserve your Webinar seat now at:
https://www2.gotomeeting.com/register/798308411

Join us on February 16, 2010 for an hour long presentation of Part 1 of the New Approaches to Neuroblastoma Therapy's (NANT) Clinical Trial Series.  This seminar will cover the NANT's non-MIBG clinical trials.  The information will be appropriate for and directed towards parents and caregivers of children with neuroblastoma.  The presentation will be given by Dr. Judith Villablanca.  She is the Medical Director of the Operations office for New Approaches to Neuroblastoma Therapy (NANT) Consortium and is active in the development and conduct of NANT Phase I/II trials of novel therapies for high risk neuroblastoma.  Dr.  Villablanca will cover the preclinical research on which the covered clinical trials are based, the eligibility criteria, and specific information regarding the clinical trials offered by the NANT.  The presentation will be followed by a question and answer period in which attendees will be able to participate.
Title:   Overview of NANT Clinical Trials - Part 1
Date: Tuesday, February 16, 2010
Time: 1:00 PM - 2:00 PM PST
After registering you will receive a confirmation email containing information about joining the Webinar.
System Requirements
PC-based attendees
Required: Windows® 2000, XP Home, XP Pro, 2003 Server, Vista
Macintosh®-based attendees
Required: Mac OS® X 10.4 (Tiger®) or newer

 

Posted 8 Feb 2010 8:39 AM by Mark Dungan
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There is nothing quite as devastating as hearing that word - neuroblastoma. In seconds your world is turned upside down and your normal life is but a distant memory. You are thrust into a confusing world full of fear. Your child has cancer.

We know. We have been there. The Neuroblastoma Foundation is here for you.

Welcome to our website. It is a place for you to find answers and ask questions. One of the primary goals of the Neuroblastoma Foundation is to ensure that parents, patients and health care professionals find the information they need to make the best treatment decisions possible for children and adults affected by neuroblastoma. There is a vast amount of information throughout the internet, much of which is encapsulated in medical jargon that is so complex that even many medical professionals have difficulty in interpreting its meaning. We are here to help to decipher this information and to make sure you (and your oncologist) understand exactly what it means to you. From treatment decisions to side effects we have parents and experts that have experienced it all and are willing to distill it for you.