Tanox to Present Two Abstracts on TNX-355 at 2005 ICAAC
07 Novembro 2005 - 6:24PM
PR Newswire (US)
HOUSTON, Nov. 7 /PRNewswire-FirstCall/ -- Tanox, Inc. (NASDAQ:TNOX)
will present two abstracts on its novel HIV antibody, TNX-355, at
the American Society for Microbiology's Interscience Conference on
Antimicrobial Agents and Chemotherapy (ICAAC), Dec. 16-19, 2005 in
Washington, D.C. The presentations include a late-breaking
submission that will further highlight the drug candidate's
recently announced Phase 2 Week 24 efficacy results. A second
abstract will detail TNX-355's activity against CXCR4 and CCR5
tropic viruses. Additionally, results of in vitro combination
studies with enfuvirtide will be highlighted. Phase 2 clinical
results showed that TNX-355, when combined with an optimized
background regimen, produced a considerably greater reduction in
viral load in HIV-infected patients than did placebo in combination
with optimized background therapy. The 82-patient clinical trial
met its primary endpoint and is continuing to its planned 48-week
duration. About TNX-355 TNX-355 is a humanized monoclonal antibody
that binds to CD4 receptors on the surface of CD4-positive cells,
preventing the entry of HIV particles into lymphocytes. TNX-355 is
the first antibody in development for the treatment of HIV and
AIDS. A Phase 2 clinical study demonstrated that TNX-355, plus
optimized background therapy, produces a clinical meaningful
reduction in viral load against multiple strains of HIV, without
depleting CD4-positive cells. TNX-355 was fast tracked by the Food
and Drug Administration in 2003. The fast track designation is
designed to expedite approval of therapies for life-threatening
diseases and allows for rolling new drug application (NDA)
submissions. About Tanox, Inc. Tanox is a biotechnology company
specializing in the discovery and development of biotherapeutics
based on monoclonal antibody technology. The company develops
innovative therapeutic agents for the treatment of immune-mediated
diseases, inflammation, infectious disease and cancer. Tanox's
first-approved drug, Xolair(R) (omalizumab), is the first
anti-immunoglobulin E (anti-IgE) antibody to be brought to market.
Xolair was developed in collaboration with Genentech, Inc. and
Novartis Pharma AG. Additional corporate information is available
at http://www.tanox.com/ .
http://www.newscom.com/cgi-bin/prnh/20050207/TNOXLOGO DATASOURCE:
Tanox, Inc. CONTACT: Steve Sievert of Tanox, Inc., +1-713-578-4211,
or Web site: http://www.tanox.com/
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