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Assessing abuse liability during drug development: changing standards and expectations.

Schoedel KA, Sellers EM

Clinical Pharmacology Group, DecisionLine Clinical Research Corporation, Toronto, Ontario, Canada. k.schoedel@dlcrc.com

As public health concerns have changed, regulatory expectations for assessing abuse liability of new central nervous system (CNS) drugs have increased. All CNS-active drugs with any properties indicating stimulant, depressant, hallucinogenic, or mood-elevating effects will require an evaluation of abuse liability. Abuse liability assessment involves the collection, analysis, and interpretation of data on chemistry and tampering, animal behavioral pharmacology, clinical trial adverse events (AEs), diversion and overdose, and potentially reinforcing (subjective) effects in recreational drug users.

Published 19 March 2008 in Clin Pharmacol Ther, 83(4): 622-6.
Full-text of this article is available online (may require subscription).

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Pharmacology Research Today Archive:

Volume 1 (2005)
  Issue 1 (August)
  Issue 2 (September)
  Issue 3 (October)
  Issue 4 (November)
  Issue 5 (December)

Volume 2 (2006)
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Volume 3 (2007)
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Volume 4 (2008)
  Issue 1 (January)
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  Issue 5 (May)
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