Gentium Presented Laboratory Data at XXth Congress of International Society for Thrombosis and Haemostasis; Laboratory Data Pres
August 09 2005 - 4:00AM
Business Wire
Gentium S.p.A. (AMEX: GNT) (the "Company") announced that earlier
today in Sydney, Australia, Dr. Guenther Eissner, Ph.D, Chief of
the Molecular Biology Research Laboratory for Gentium, presided
over a poster presentation at the XXth Annual Congress of the
International Society on Thrombosis and Hemostasis. The poster
presentation, "Defibrotide and Oligotide, Two DNA-Based Drugs,
Protect Human Microvascular Endothelial Cells Against
Chemotherapy-Induced Damage and Activation," reports that data
showed the drugs' potential ability to protect human endothelial
cells from chemotherapy-induced activation, transendothelial
migration and apoptotic damage and may eliminate the increased
allogenicity of cytotoxic T cells (CTL). In laboratory studies
Defibrotide showed anti-thrombotic, anti-ischemic, and
pro-fibrinolytic activity with endothelium protective effects.
Defibrotide, the company's lead product candidate in the U.S., is
an investigational drug that has been granted Orphan Drug status by
the U.S. FDA to treat veno-occlusive disease (VOD) with multiple
organ failure ("Severe VOD") and Fast Track designation to
facilitate development and expedite the agency's review of the
drug. Dr. Massimo Iacobelli, Gentium's scientific director,
commented on the outcome of the study, "This is very encouraging
data as to the effects of conditioning with Defibrotide and
Oligotide prior to allogeneic stem cell transplantation and cancer
chemotherapy of solid tumors, where in both cases, the
stabilization of the vascular endothelium is one of the pivotal
steps to cure." About VOD Severe VOD is a potentially
life-threatening condition in which some of the veins in the liver
are blocked as a result of toxic cancer treatments such as
chemotherapy, radiation, hormone therapy and bone marrow and stem
cell transplants. It is estimated that 80% of patients with Severe
VOD die with 100 days. There are no currently approved treatments
for Severe VOD. About the Company Gentium S.p.A. is a
biopharmaceutical company located in Villa Guardia (Como), Italy
that is focused on the research, discovery and development of drugs
derived from DNA extracted from natural sources and drugs which are
synthetic oligonucleotides (molecules chemically similar to natural
DNA) to treat and prevent a variety of vascular diseases and
conditions related to cancer and cancer treatments. Cautionary Note
Regarding Forward-Looking Statements This press release contains
"forward-looking statements." In some cases, you can identify these
statements by forward-looking words such as "may," "might," "will,"
"should," "expect," "plan," "anticipate," "believe," "estimate,"
"predict," "potential" or "continue," the negative of these terms
and other comparable terminology. These statements are not
historical facts but instead represent the Company's belief
regarding future results, many of which, by their nature, are
inherently uncertain and outside the Company's control. It is
possible that actual results may differ, possibly materially, from
those anticipated in these forward-looking statements. For a
discussion of some of the risks and important factors that could
affect future results, see the discussion in our Prospectus filed
with the Securities and Exchange Commission under Rule 424(b)(4)
under the caption "Risk Factors."
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