Advancing Rare Disease Drug Discovery: Navigating the Path to an IND

Advancing Rare Disease Drug Discovery: Navigating the Path to an IND

Program Summary

Therapies to treat rare and undiagnosed diseases are in high demand in a favorable regulatory environment1. Thus, it is critically important to optimize the discovery and development of such therapies by creating – and following – the most efficient path to an investigational new drug (IND) filing. How do we do just that? In-depth scientific investigation, combined with efficiently planned study paradigms, are key to moving therapeutics along the drug development continuum.

Join us for a meeting of the minds on Monday, May 15th in Cambridge, MA as we host a one-day symposium to explore the challenges and success stories of rare disease drug discovery. Hailing from biotech, pharma, foundations, and academia, our diverse panel of speakers will share case studies and best practices. In addition to our scheduled presentations, the agenda will include panel discussions and networking breaks so bring your questions.

Don’t miss this opportunity to gain valuable insight on managing rare disease drug development through the preclinical pipeline.

1 41% of newly approved drugs in 2016 were for rare disease indications

Registration (Waitlist)                      

Please note: We have reached capacity for this event. If you would like to be included on the waitlist, please click "Register Now" below and we will contact you once an opening becomes available.

This complimentary symposium, sponsored by Charles River, includes breakfast, lunch, refreshment breaks throughout the day as well as a networking reception after the symposium.  

 

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  • When

  • Monday, 15 May, 2017
    8:00 AM - 6:30 PM

  • Where

  • Boston Marriott Cambridge
    50 Broadway
    Cambridge, Massachusetts 02142
    USA
    1-617-252-4402

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