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2nd Adaptive Clinical Trials Symposium (description)

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Category:Health & Wellness
Address:1800 Market Street, Philadelphia, Pennsylvania, United States of America 19103
Phone:9179320431
Event dates:3/18/2019 - 3/19/2019 (This event has already taken place)
Event web site:http://go.evvnt.com/342144-0?pid=5188
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Speakers/Presenters:

Topics to be Covered:

  • Conferences
  • Science
  • Health and Medicine
  • Pharmaceuticals
  • Clinical
  • Drug Development
Contact:eschriver@exlevents.com
Organizer phone:9179320431
Offering type:Conference
Specialty:Data not provided
Event frequency:Never
First Meeting:
Total events:
Est. attendance:
Target audience:Any
Other target audiences:
Host Sponsor:ExL Events, a division of Questex, LLC
Est. # of exhibitors:
Currency:US Dollars
Language:Data not provided
CE Credits:
Organizer URL

Description:

Adaptive clinical trial design allows for modifications to the trial after it begins without damaging the integrity of the study. An adaptive design allows for a more proficient use of capital and resources through shorter timeframes and fewer patients. Using adaptive design sponsor organizations can allocate resources more efficiently without lowering standards and therefore are able to accelerate the clinical development process.

The point at which data is reviewed for an adaptive trial is known as an interim analysis. During the interim analysis, trial organizers review and analyze data before all the “needed” data is collected. This is the pivotal point where an adaptive trial differs from a traditional design. If a sponsor organization notices that something needs to change within their protocol they can make the necessary changes here, without compromising the trial or starting over — ultimately saving time and resources.

The 2nd Adaptive Clinical Trials Symposium will teach cross-functional stakeholders the importance of statistics, data management, and operations through interim analysis for adaptive clinical trials.

Top Five Reasons to Attend
1. Discover best practices for planning and managing an adaptive trial
2. Learn, from true industry experiences, how to get drugs to market faster at less cost
3. Analysis of FDA guidance and tips to navigate through the gray areas associated with an adaptive design
4. Network with peers and top industry professionals in an intimate environment
5. Understand the role of interim analysis in adaptive design

Schedule:

8:00 am - 5:30 pm

Registration Fee Details:

Early Bird Pricing Register by February 1, 2019: USD 1895.0,
Standard Pricing: USD 2095.0,
Onsite Pricing: USD 2195.0

Other items that tuition includes:

Travel and hotel arrangements:

 
 
Contact Person:Emily Schriver
Contact Emaileschriver@exlevents.com
Organizer State/Province: (Outside US)
Organizer CountryData not provided
Organizer Phone9179320431
Structural makeupData not provided
Host Sponsor; Other SponsorsExL Events, a division of Questex, LLC
Event Site/VenueSonesta Philadelphia Downtown Rittenhouse Square
Event sold out?No
Multiple locations or dates?No
Statistics available for most recent event held in:NA
Average number in event attendance of:
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Number in attendance of:
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Target BoundariesInternational
Is Registration contact information the same as Organizer Contact above?NA
Registration Contact:
Registration E-Mail:
Registration Phone:
Registration Fax:
Web Page https://go.evvnt.com/342144-2?pid=5188
Can one register for your CE on your web site?NA
Can registration be made by snail (regular) mail?NA
Online housing reservations: 
 
Do you have additional written or AV materials for sale?No
If so, are they available for non-attendees as well as those attending?NA
Is full tuition necessary to ensure registration?No
Will there be shuttle service available?NA
Additional notes:

URL:
Brochure: https://go.evvnt.com/342144-3?pid=5188

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