Anadis Commercializing "BioGard" Adjunctive Therapy for HIV & AIDS
04 Setembro 2008 - 7:00AM
Business Wire
Anadis (ASX: ANX; OTC: ANDIY) announced today its commercialization
of a new product, BioGard�, intended to maintain gastrointestinal
and immune system health. The specific formulation may be of
particular clinical benefit in persons undergoing antiretroviral
therapy for HIV/AIDS. The product is intended to enhance current
treatment regimens and improve the efficacy of immune system repair
during highly active antiretroviral treatment (HAART) treatment.
The gastrointestinal immune system is increasingly recognized as
having an important role in the progression of HIV-related immune
depletion and local gastro-intestinal symptoms have been a great
concern to HIV/AIDS patients. The target market for the product
includes over 1 million patients in the U.S., 2 million in Europe
and Central Asia and more than 30 million worldwide. BioGard is
intended to be marketed as a medical food, used under medical
supervision, although available for purchase over-the-counter, and
is expected to be launched in 2009 following results from a phase
IIIb/IV multi-site clinical trial beginning this year that is an
advanced stage of planning. The product�s active ingredient is a
proprietary oral formulation of antigen-targeted Bovine Colostrum
Powder (BCP) that has been approved by Australia�s regulatory
agency, the Therapeutic Goods Administration (TGA). The product
will be first available in tablet format manufactured and packed in
a TGA registered GMP tableting facility. Like other Anadis BCP
products, the freeze-dried active ingredients in BioGard tablets is
obtained from commercial dairy cow herds utilizing the patented
Anadis hyper-immunization technology and deploying unique
collection processes to assure quality . The BSE free cows in these
herds, as well as being vaccinated for routine cattle pathogens,
have been vaccinated with a proprietary Anadis vaccine containing
important lipopolysaccarides found in gram negative bacterial cell
walls that are implicated as key drivers of AIDS pathogenesis. Data
supporting this work was first presented recently by scientists
from Murdoch Children�s Research Institute, Royal Children�s
Hospital, Parkville, Victoria and the Department of Microbiology
& Immunology, University of Melbourne at the Australian Society
for Microbiology annual meeting held in Melbourne. Anadis is now in
advanced discussion with a major AIDS-research institution to test
the efficacy of BioGard in a multi-site, randomized double-blind,
placebo controlled study. The goal of the study is to measure the
effect of combination antiretroviral therapy intensification with
BioGard on CD4+ outcomes in HIV-1 infected individuals with
suboptimal CD4 response to therapy despite prolonged virologic
suppression. Details of the study will be released at a later time.
Dr. Zeil Rosenberg, CEO of Anadis stated: �Combination
anti-retroviral therapy (cART) intensification and use of our new
antigen-targeted bovine colostrum added to stable cART may help
restore immunological integrity of the intestinal mucosal barrier
thereby controlling microbial translocation, diminishing immune
activation and resulting in better CD4+ cell reconstitution. This
is expected to significantly improve the efficacy and safety
profile of drugs in the HIV area.� Dr. Oren Fuerst, VP Business
Development of Anadis, stated: �BioGard was developed based on a
novel approach related to the inflammation process and is another
manifestation of the versatility of our platform. We continue to
develop and rapidly commercialize products that are both important
to large populations and which have a clear commercial market. In
this case, our products may increase the efficacy and safety of
drugs with current revenue in excess of $5bn per year.� Anadis
Limited (ASX: ANX; OTC: ANDIY) is a biopharmaceutical company
focused on antigen-primed, dairy-derived health products. Anadis�
proprietary technology enables it to rapidly develop polyclonal
antibody and other proteins-based solutions to a range of important
diseases. The all-natural colostrum-derived platform, its high
safety profile when administered orally and the proprietary methods
of manufacturing, allows for short time-frame from bench to market
with high manufacturing scalability.
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