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Dear All,
I am trying to construct a profile objectives of a lead compound
for Cathepsin K inhibitor to be developed as a potential drug for
osteoporosis. I have done this exercise in the past in the infectious
disease area setting up criteria for choosing a lead compound from
discovery hits based on its pharmacokinetic profile in early
pharmacokinetic studies in rodent . But as we all know the site of
inhibiting the extracellular enzyme cathepsin K is in the osteoclast,
the pharmacokinetic parameter criteria have to be set appropriately to
choose the right compound for development to get a successful clinical
outcome. Any comments or reference to set these PK criteria would be
appreciated.
Jehangir K. Khan, M.Pharm
Biopharmaceutics & Pharmacokinetics
NAEJA Pharmaceutical Inc.
Edmonton, AB, Canada
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Copyright 1995-2010 David W. A. Bourne (david@boomer.org)