Elixir Medical Corporation Licenses Myolimus™
From Novartis Pharma AG for Site-Specific Drug Delivery Applications
SUNNYVALE, Calif. (PRWEB / Business Wire EON) October 10, 2008 --
Elixir Medical Corporation announced today that the company entered into
a co-exclusive worldwide license agreement with Novartis Pharma AG
granting Elixir the rights to utilize the drug Myolimus with Elixir’s
vascular and other site-specific drug-delivery applications. In
addition, Elixir has an exclusive worldwide license for use of Myolimus
in fully biodegradable stents. "Elixir is committed to be a leader in
the drug eluting stent market through the efficient development of a
broad and innovative portfolio of DES products to better address
physician and patient needs," said Motasim Sirhan, chief executive
officer of Elixir Medical Corporation. “The
license agreement with Novartis Pharma AG for Myolimus enhances our
capabilities to develop innovative product platforms for our physicians
and patients.”
Myolimus, a macrocyclic lactone in the same family as Rapamycin, has
demonstrated impressive versatility, stability, and a broad therapeutic
index. The macrocyclic lactone drugs represent the most widely utilized
drug family for drug eluting stent applications and have an established
safety and efficacy profile. Elixir observed positive results from
evaluating the safety and effectiveness of Myolimus for the prevention
of restenosis through extensive pre-clinical testing including in vivo
animal studies and in vitro testing conducted over the past several
years.
Elixir has completed three separate first-in-man clinical studies
evaluating the therapeutic effectiveness of the company’s
Myolimus-eluting coronary stent systems. These studies used the company’s
proprietary stent platform and three proprietary polymer technologies.
In the first study, the stent platform incorporates a proprietary
durable polymer coating with an established safety profile designed to
have a minimal polymer load and the lowest known ‘olimus’
drug dose. In the second study, the stent platform incorporates a
proprietary biodegradable polymer coating designed to biodegrade within
three to six months. In the third study, the stent platform incorporates
a different proprietary biodegradable polymer coating designed to
biodegrade within six to nine months. Both biodegradable coating
platforms offer the potential of achieving the desired effectiveness and
resulting in a more biocompatible stent surface similar to bare metal
stents (BMS).
"We also intend to utilize Myolimus in a broad range of site-specific
drug delivery therapeutic applications including a fully biodegradable
stent program," commented Mr. Sirhan on the special properties and
opportunities for Myolimus.
Elixir continues to make excellent progress with its proprietary
macrocyclic lactone drug Novolimus. Twelve-month follow up from the
Excella I first-in-man study has been successfully completed and will be
presented at the upcoming TCT DES Summit. The company will initiate the
Excella II multi-center randomized clinical trial in Q4’
2008. Data from Excella II will be submitted for CE mark approval of the
Novolimus eluting coronary stent system.
TCT Conference Events
-
Elixir will present in-vivo preclinical animal studies and early
results from the first two Myolimus FIM clinical studies as well as
the Novolimus FIM clinical study at the 20th annual Transcatheter
Cardiovascular Therapeutics DES Summit (TCT 2008) on Monday, October
13, 2008, in Washington, D.C.
-
Elixir will host a breakfast symposia on Wednesday, October 15, from
7-8 am to present on the company’s DES
Programs including design, pre-clinical testing, and FIM clinical
study results.
Chair: Professor Patrick W. Serruys, MD, Ph.D.
Faculty: Alexandre Abizaid, M.D., Ph.D., Peter Fitzgerald, M.D., Ph.D.,
Guy Leclerc, M.D., John Ormiston, M.D., Ph.D., Ch.B., Wolfgang Rutsch,
M.D., Ph.D.
About Elixir Medical
Elixir Medical Corporation, a privately held company headquartered in
Sunnyvale, California, develops products that combine state-of-the-art
medical devices with advanced pharmaceuticals to provide innovative
treatment solutions to patients worldwide. The company’s
next-generation drug-eluting stent systems are designed to optimize
localized drug delivery to provide a safe and effective treatment for
cardiovascular patients. For more information, visit www.elixirmedical.com.
See the original story at: http://eon.businesswire.com/releases/2008/10/prweb1454724.htm
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