Purdue
Pharma L.P. will demonstrate an analysis of data from completed clinical trials
for Butrans Transdermal System CIII with the American Pain Society's (APS) 31st
Annual Scientific Seminar. The research has an evaluation of supplemental
analgesic use and pain marks along the 7-day dosing interval.
The
poster will probably be presented with the APS meeting in Honolulu, HI on
Friday, May 18 at 8:45 AM HAST: Butrans (buprenorphine) Transdermal Structure
and 7-day Analgesic Performance.
Butrans
is indicated for the administration of moderate-to-severe chronic pain in
affected individuals requiring endless, hysterical opioid analgesic for some
time. Accepted by the U.S. Food and Drug Administration (FDA) in June 2010,
Butrans is the first transdermal structure that in fact delivers steady release
of a typical active component, buprenorphine, for one week.
Butrans
is a Schedule III opioid medication and might be abused in a manner similar to
other opioid agonists, official or illicit. Engaging with the FDA, Purdue
Pharma L.P. created a Risk Evaluation and Mitigation Strategy (REMS) for
Butrans that includes a Treatment Guide, Factors to make certain Safe Use, for
instance a healthcare provider training manual, and a timetable for submitting
evaluations of typical REMS.