REMOXY
Pain Therapeutics to Regain Full Rights to REMOXY(R)
AUSTIN, Texas, Oct. 27, 2014
(GLOBE NEWSWIRE) -- Pain Therapeutics, Inc. (Nasdaq:PTIE) today reported
it believes it will regain full development and commercial rights to
REMOXY from Pfizer, Inc. On Friday, October 24th, Pfizer
hosted a conference call with us during aftermarket hours to inform us
of their intention to terminate development of REMOXY. Actual
termination will become effective six months from today, pursuant to the
terms of a Collaboration Agreement.
"We are grateful to Pfizer for their substantial investment in REMOXY
over the years and now for this opportunity to regain full control of
REMOXY", said Remi Barbier, President & CEO. "It's a privilege to
reacquire worldwide rights to an unencumbered Phase III asset that
targets a $2 billion market. We look forward to the prospects of
resubmitting the REMOXY NDA under our control. We are also enthusiastic
about initiating discussions with potential pharmaceutical partners
around this drug asset."
Under the contractual terms of a termination, all data, documents and
remedial work conducted and paid for by Pfizer with respect to REMOXY
will transition to us over the coming months, including results of five
recently completed clinical studies.
Today's Conference Call
We will host a conference call today, Monday, October 27th at 8 a.m.
Central Time/9:00 a.m. Eastern Time to discuss REMOXY and to respond to
questions from investors. Participants may access the call by dialing
1-877-407-4018 in the U.S. or 1-201-689-8471 outside the U.S. The call
will be webcast live on the Company's website at www.paintrials.com. A
replay of this conference call will be available through November 6th
by dialing 1-877-870-5176 in the U.S. or 1-858-384-5517 outside the U.S.
The replay access code is 13594560.
About REMOXY®
Our lead drug candidate, REMOXY (oxycodone) Extended-Release Capsules
CII, is an oral formulation of oxycodone for the management of
moderate-to-severe pain when a continuous, around-the-clock opioid
analgesic is needed for an extended period of time. We developed REMOXY
to discourage common methods of tampering and misuse.
About FENROCK™
FENROCK is a new, proprietary abuse-deterrent pain patch in pre-IND
stage of development. Our goal with FENROCK is to mitigate the abuse,
misuse, overdose and death associated with currently marketed fentanyl
patches. The active drug ingredient in the FENROCK patch is fentanyl
(CII), a highly potent synthetic opioid typically used to manage severe
cancer pain.
About Pain Therapeutics, Inc.
Pain Therapeutics, Inc. is a biopharmaceutical company that develops
novel drugs. The FDA has not approved our drug candidates for commercial
sale. For more information, please visit www.paintrials.com.
Note Regarding Forward-Looking Statements
This
press release contains forward-looking statements within the meaning of
the Private Securities Litigation Reform Act of 1995, including
statements about our prospects for growth, intellectual property
protection, market size or growth, competitive position, regulatory
agency action, and the anticipated development, timing, data readouts
and therapeutic scope and value of our development stage products. You
should not place undue reliance on these
statements. These statements involve significant risks and
uncertainties. Our results may differ materially from those contained in
such statements, including, among others: our inability to protect our
intellectual property rights and to have sufficient rights to
commercialize our products; product competition; clinical trials of our
products may fail or not be initiated or conducted in a timely manner;
our products may show insufficient therapeutic effects or unacceptable
safety profiles; adverse decisions by regulatory authorities; existing
preclinical and clinical data with respect to our products may not be
indicative of future clinical or commercial results; and the inability
to manufacture successfully our products. Additional factors that could
cause actual results to differ significantly from those projected in our
forward-looking statements are discussed in our Annual Report on
Form 10-K, Quarterly Reports on Form 10-Q and recent Current Reports on
Form 8-K. Our forward-looking statements are based on our current
beliefs and expectations and speak only as of the date of this press
release. We do not undertake any obligation to update any
forward-looking statements. The term "Abuse-deterrent" is not intended
to designate an indication or a medical claim but rather a general
description of agents designed to address the misuse, abuse and
diversion of opioids. Oxycodone and fentanyl are controlled-substances
(CII) with high potential for abuse. The active ingredient in all
opioids (including REMOXY and FENROCK are highly addictive.
CONTACT: For More Information Contact:
Peter S. Roddy
Vice President and Chief Financial Officer
Pain Therapeutics, Inc.
proddy@paintrials.com
(512) 501-2450
Barbara Ryan
FTI Consulting
Barbara.ryan@fticonsulting.com
(212) 850-5679
No comments:
Post a Comment