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Clinical Trials Phase I & IIA Summit

Clinical Trials Phase I & IIA Summit

Categories

Date of beginning

Thursday, 17 October 2019

Duration

2 days

City

Philadelphia

Country

United States

Contact

Yuliya Sheflyand

E-Mail

This email address is being protected from spambots. You need JavaScript enabled to view it.

Memo

Sponsors often take for granted the fact that early phase trial design and operations can make or break future studies. When hard data is severely limited and is used to predict well beyond its boundaries, the quality of that data is absolutely paramount. The data obtained from phase 1 first-in-human studies through phase 2 proof-of-concept and dose range finding studies are vital to effectively designing future registration studies. Early phase clinical trials should be safe experiments on humans, not small-scale phase 3 trials. Therefore, it is beneficial to intelligently optimize early phase clinical activity to ensure successful trial execution and regulatory approval.TOP FIVE REASONS TO ATTEND*Implement adaptive study designs and predictive models to successfully accelerate early phase trials*Improve vendor identification and communication from negotiation to study execution*Overcome the evolving challenges of patient recruitment and retention for different diseases*Leverage techniques to help identify genetic predisposition and risk factors for adverse events and drug reactions*Discuss innovative strategies to optimize early phase clinical trial operations URLs: Brochure https://go.evvnt.com/495324-2?pid=5569Tickets https://go.evvnt.com/495324-3?pid=5569 Prices:Standard: USD 2095.00,Early Bird: USD 1895.00,Onsite Pricing: USD 2295.00. Speakers: Michel Azoulay, Global Oncology Leader, SANOFI CLINICAL OPERATIONS STRATEGY, Wesley Day, Lead Global Clinical Development, MTDA, Martin Gutierrez, M.D., Director of the Drug Discovery , JOHN THEURER CANCER CENTER, Chelsea McCabe, Project Manager, JOHN THEURER CANCER CENTER, Jim Nissel,Director, Clinical Trial Management, Translational Development – Clinical Pharmacology, CELGENE, Rosemarie Pincus, Principal Medical Writing Scientist, Oncology Division, JOHNSON & JOHNSON, Laura Vessey, Director, Early Clinical Development, MERCK, Tami Crumley, Principal Scientist, Translational Pharmacology, MERCK, Bruce Morimoto, Vice President, Drug Development Operations, ALKAHEST, Paul Rothenberg, Executive Director, Strategic Product Development, COVANCE, Pranab Mitra, Associate Principal Scientist, MERCK, William B. Smith, President, NEW ORLEANS CENTER FOR CLINICAL RESEARCH. Time: 8:00 am to 5:00 pm. Venue details: Sonesta Philadelphia Downtown Rittenhouse Square, 1800 Market Street, Philadelphia, 19103, United States.