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ICORD 2009: Facilitating Cooperation in Regulatory Efforts Timothy Cote, MD MPH Director, FDA Office of Orphan Products Development, Food and Drug Administration, Rockville, MD, USA Monday, Feb 23, 2009
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International Collaborative Regulatory Actions Designations The joint form Annual reports Exchange Grants Neglected tropical diseases The Science of Small Clinical Trails Search for Forgotten Orphan Drugs of Special Promise---We must be accountable in holding the People’s data.
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The search for forgotten orphan drugs of promise 25 years! 1,892 orphan designations as of August 2008 (1,960+ now) and 334 marketing approvals---what happened to the rest? Some were junk. Some were toxic. Some were forgotten. Drug development is not a strictly Darwinian process where the fit (i.e. safe/effective) always win.
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Definition: Forgotten Orphan Drugs? Some IND* data was submitted to FDA IND was begun before Jan 1 2006 No record of recent activity on the IND. Hasn’t been approved for its designated orphan indication, another orphan indication or a common disease (i.e. not on the market). *Investigational New Drug, a file of incoming data submitted to FDA.
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1892 Designations 1983 through 8/31/2008 327 Approved Orphan Indication 361 Recent INDs 2006 through 8/31/2008 316 No IND Available 137 Approved For another Orphan Indication 572 Older Designations, Not-Approved with an IND 179 Approved For a Common Disease Indication 23 Other INDs Status 88 CBER Biologics 59 WithdrawnI NDs 26 Terminated INDs 70 Inactive INDs 306 Active INDs 266 Forgotten Orphans Forgotten Orphans Waiting at FDA
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Plan: Re-examine Forgotten Orphans Study design Study enrollment Study results for Efficacy Study safety signals Then…if there are forgotten orphans of great promise; reinvigorate them!
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Summary: Rare Diseases Erase National Boundaries International body of science International pharmaceutical industry International network of patients To be effective proponents of developing drugs for rare diseases, regulators must work internationally.
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