Message #51 From:
NewsBot Date: December 18, 2006 05:00:00 AM
DEPO News Depomed Delivers Notice of Breach and Demand for Arbitration to Esprit Pharma
MENLO PARK, Calif.--(BUSINESS WIRE)--Depomed, Inc. (NASDAQ:DEPO) today announced that it has delivered a
notice to Esprit Pharma, Inc. regarding Esprit’s
breaches of the parties’ Exclusive License and
Marketing Agreement for ProQuin®XR, a once-daily extended release formulation of ciprofloxacin for
the treatment of uncomplicated urinary tract infections. The breaches
involve, among other matters, Esprit’s failure
to make the $10 million license fee payment due to Depomed under the
contract on December 15, 2006, and to use commercially reasonable
efforts to market ProQuin XR.
As the license agreement provides for arbitration of disputes under the
contract, Depomed has also filed a demand for binding arbitration
related to Esprit’s breaches of the contract.
The demand seeks in excess of $105 million in damages, which includes
all license payments, minimum royalty payments, and expected additional
royalty payments due through the life of the patents licensed under the
contract.
About Depomed, Inc.
Depomed, Inc. is a specialty pharmaceutical company utilizing its
innovative AcuFormTM drug delivery technology to
develop novel oral products and improved, extended release formulations
of existing oral drugs. AcuForm-based products are designed to provide
once daily administration and reduced side effects, improving patient
convenience, compliance and pharmacokinetic profiles. ProQuin®
XR (ciprofloxacin hydrochloride) extended-release tablets have been
approved by the FDA for the once daily treatment of uncomplicated
urinary tract infections and are currently being marketed in the United
States. In addition, once daily GlumetzaTM
(metformin hydrochloride extended release tablets) has been approved for
use in adults with type 2 diabetes and is currently being marketed in
the United States and Canada. The company is conducting a Phase III
trial in postherpetic neuralgia and has completed a Phase II trial in
diabetic peripheral neuropathy with its product candidate, Gabapentin GRTM.
Additional information about Depomed may be found at its web site, www.depomedinc.com.
“Safe Harbor" Statement under the
Private Securities Litigation Reform Act of 1995. The statements
that are not historical facts contained in this release are
forward-looking statements that involve risks and uncertainties
including, but not limited to, those related to our relationships and
disputes with collaborative partners; expectations regarding
commercialization of our products; our research and development efforts,
including pre-clinical and clinical testing; regulation by the FDA and
other government agencies; the timing of regulatory applications and
product launches; and other risks detailed in the company's Securities
and Exchange Commission filings, including the company's Annual Report
on Form 10-K and most recent Quarterly Report on Form 10-Q. You are
cautioned not to place undue reliance on these forward-looking
statements which speak only as of the date hereof. The company
undertakes no obligation to publicly release the result of any revisions
to these forward-looking statements that may be made to reflect events
or circumstances after the date hereof or to reflect the occurrence of
unanticipated events.