 |
NitroMed and Merck Form Strategic Collaboration
Companies Enter Multi-year Agreement to Research
and Develop
Nitric Oxide Based Medicines
BEDFORD, MA
January 7, 2003
NitroMed, Inc. today announced that they have formed a multi-year
research collaboration with a subsidiary of Merck & Co., Inc.
(NYSE:MRK) to develop nitric oxide (NO) based medicines.
"This collaboration allows us to leverage the strength of our
proprietary and broad technology platform, NitRx™ with Merck's
proven research and development programs," said Michael D. Loberg,
Ph.D., Chief Executive Officer of NitroMed. "We are very excited
about the research and commercial prospects that can be developed
with our combined expertise. Merck has been a pioneer and a leader
in drug discovery and research and we appreciate that this collaboration
recognizes the value of our research programs."
Although specific details of the agreement were not disclosed, the
collaboration is based on NitroMed's strong research program that
has made significant progress in the proprietary synthesis of NO-based
medicines. NitroMed will benefit from Merck's investment in its research
program. The agreement secures multi-year funding for scientists and
equipment. Merck has agreed to pay an up-front fee, certain research-based
milestones, and royalty payments. Merck will provide the commercialization
expertise in the partnership.
Dr. Loberg commented, "Collaborative partnerships are a key element
of our business strategy. We have a strong research program that is
making significant progress in the proprietary synthesis of NO-derived
medicines. Our alliance with Merck underscores our commitment to maximize
and optimize the discovery and commercialization process necessary
to bring safe and effective NO-derived medicines to people."About
NitroMed, Inc.
NitroMed, Inc. is a private biopharmaceutical company pioneering the
development and commercialization of nitric oxide (NO)-enhanced medicines.
The Company has developed a broad technology platform, NitRx™,
for delivering therapeutically active NO, a well-known mediator of
biological functions. Using this platform, the Company has developed
a diverse pipeline of novel NO-based molecules, as well as existing
medicines enhanced with NO-donors. NitroMed's clinical areas of focus
for its NO-enhanced medicines are based on the treatment and/or prevention
of cardiovascular disease and inflammatory diseases.
The Company's most advanced stage product is BiDil®, a drug designed
to improve survival in African Americans with heart failure. BiDil
is a combination drug containing isosorbide dinitrate and hydralazine
hydrochloride. A pivotal confirmatory trial, in 600 African American
men and women called A-HeFT™ is on-going and results are expected
in early 2004.
It has been estimated that 5 million Americans have heart failure.
About 725,000 of those are African Americans. Research has demonstrated
that African American patients are twice as likely as white patients
to suffer from heart failure. In addition, death rates from heart
failure are more than twice as high in African American patients than
in white patients. This disparity in outcomes is attributed to many
factors, including a pathophysiology found primarily in African American
patients that may involve nitric oxide (NO) insufficiency arising
from either reduced NO production, enhanced NO inactivation or both.
BiDil may work by restoring depleted NO levels and by protecting the
NO that is formed naturally in the vascular endothelial cells of these
patients. For additional information about NitroMed, please consult
www.nitromed.com.
|
 |
|