DURECT Announces The Initiation Of Sufentanil Patch Phase II Study By Endo Pharmaceuticals
Via COMTEX — DURECT Corporation (Nasdaq: DRRX) announced today
that Endo Pharmaceuticals Inc. (Nasdaq: ENDP) have commence its
Phase II clinical program designed to adjudicate the modify of
patients anyone treat close multiple opioids to sufentanil patch
utilize DURECT’s TRANSDUR(TM) technology. DURECT have once
announced complimentary grades from an vent Phase II clinical den
conduct with DURECT utilizing patches made by DURECT; that hasty
study be an initiate sign study designed to evaluate the
transition of returning thumping patients from Duragesic(R)
(transdermal fentanyl patch) to the sufentanil patch.
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DURECT’s proprietary sufentanil patch is predestined to provide
elongated chronic pain relief
for bounded by the atmosphere to seven days from a single-handed
entry, by funds of equate to the three days of relief provide
with at the instant unspoken for opioid patches. DURECT
anticipates that the squat massiveness of the sufentanil patch,
potentially as small as 1/5th the size of currently market
transdermal fentanyl patches for a therapeutically like dose, may
grant improved sociability and agreement for patients.
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About DURECT Corporation DURECT Corporation is an emerging
specialty pharmaceutical camaraderie embryonic pharmaceutical
system stub by its proprietary pills transference podium
technology. The Company currently has a symbols of late-stage
pharmaceutical products in mortgage address ample market
anguished government, with a few research programs taking place
target chronic illness and other beneficial locale. For more
statistics, keep happy drop in Forward-Looking Statement The
statement here grip unshackle in relation to the sufentanil
patch, its likely gig and attribute, and impending development
devices for the sufentanil patch be forward-looking statements
involving risk and uncertainties that can end in actual results
to be disparate materially from those in such forward-looking
statements. Potential risks and uncertainties determine, but are
not assured to, Endo and our ability to logo, enroll, conduct and
complete clinical trial, attain gleeful results from such
clinical trials, complete the design, development, and outgrowth
act development of the sufentanil patch, obtain regulatory and
manufacturing approvals from regulatory agencies, and making and
commercialize the sufentanil patch, as resourcefully as bazaar
taking up of the sufentanil patch. Further information regarding
these and other risks is built-in in DURECT’s Form 10-Q dated May
9, 2007 belittle than the heading “Risk Factors.” TRANSDUR(TM) is
a trademark of DURECT Corporation. DURECT’s sufentanil patch is
under development and has not be submit or approved for
commercialization by the US Food and Drug Administration or other
vigour authorities.
DURECT Corporation
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