Bioniche Phase III Clinical Trial with Urocidin(TM) Given Continued Green Light by DMC



    BELLEVILLE, ON, Aug. 24 /CNW/ - Bioniche Life Sciences Inc. ("Bioniche";
TSX: BNC), a research-based, technology-driven Canadian biopharmaceutical
company, today provided an update on its Phase III clinical program evaluating
Urocidin(TM) in the treatment of bladder cancer. Recruitment has been
completed in its Phase III registration trial evaluating Urocidin in the
treatment of non-muscle-invasive bladder cancer that is refractory
(unresponsive) to the current standard immunotherapy - Bacillus
Calmette-Guérin (BCG).
    The Data Monitoring Committee (DMC) held its ninth meeting regarding this
clinical trial last week. After its meeting, the Committee has recommended
that Bioniche "continue the trial unmodified until the next scheduled or
triggered meeting." The next scheduled meeting of the Committee is scheduled
to occur in October.
    The DMC is an independent group that acts in an advisory capacity to the
Company. Its role is to evaluate the progress of the clinical trial, including
monitoring the safety and efficacy data generated in the trial. On a regular
basis, the DMC reviews study results, evaluates the incidence of adverse
events, determines whether the basic trial assumptions remain valid, and
evaluates whether the overall integrity, scientific merit and conduct of the
study remain acceptable.
    Data from the full cohort of 105 high-grade bladder cancer patients from
this trial, coupled with additional safety information to be collected from a
second clinical trial that is expected to start later this year, will be used
to support regulatory submissions under the FDA's Accelerated Approval
program.

    Second Phase III Registration Trial

    Bioniche is working with its new licensing partner, Endo Pharmaceuticals
Inc., on setting up clinical trial sites for a second registration trial that
will directly compare the efficacy and safety of Urocidin with BCG in the
first-line treatment of non-muscle-invasive bladder cancer.
    In September, 2007, the Company announced that an agreement had been
reached with the FDA under the Special Protocol Assessment (SPA) procedure on
the design of the trial, including its endpoints, data analysis and conduct.
It provides assurance that, if the trial endpoints are met, they will serve as
the basis for product approval under a Biologics Licensing Application (BLA).
An SPA gives a clear pathway to registration of Urocidin when the trial
endpoints are achieved. This indication for MCC received Fast Track
designation by the FDA last year.

    About Bladder Cancer

    In North America, bladder cancer is the fourth most common cancer in men
and in the top ten for women. In the United States, approximately 70,000
patients are newly diagnosed with bladder cancer each year. In addition, the
cancers of many previously-diagnosed patients remain unresolved, sometimes
leading to cystectomy (bladder removal) or death. Approximately 70 percent of
bladder cancer patients have the non-muscle-invasive form of bladder cancer at
diagnosis and, on appropriate regulatory approvals, might be eligible for
multiple treatments with Urocidin.
    Non-muscle-invasive bladder cancer is a form of bladder cancer localized
in the surface layers of the bladder that has not yet spread into the deeper
muscle layer. This form of bladder cancer is treated predominantly by
urologists using surgical resection and intravesical infusion therapy.
Urocidin is an intravesical infusion therapy, administered via trans-urethral
catheter into the bladder.

    About Urocidin(TM)

    Urocidin is a formulation of MCC, a sterile mycobacterial cell wall-DNA
complex composition that has a dual mode of action: immune stimulation and
direct anticancer activity. Urocidin is formulated for the treatment of
bladder cancer, where it is administered by trans-urethral catheter directly
into the bladder, coming into contact with immune system cells and bladder
cancer cells. Industry Canada's Industrial Technologies Office (formerly
Technology Partnerships Canada) has contributed to the development of the
Company's mycobacterial cell wall technologies by means of a C$9.6 million
loan that is recoupable from sales.

    About Bioniche Life Sciences Inc.

    Bioniche Life Sciences Inc. is a research-based, technology-driven
Canadian biopharmaceutical company focused on the discovery, development,
manufacturing, and marketing of proprietary products for human and animal
health markets worldwide. The fully-integrated company employs approximately
200 skilled personnel and has three operating divisions: Human Health, Animal
Health, and Food Safety. The Company's primary goal has been to develop
proprietary cancer therapies supported by revenues from marketed products in
human and animal health. Bioniche has been named one of the Top 50 Best Small
and Medium-Sized Employers in Canada for 2009. For more information, please
visit www.Bioniche.com.

    Except for historical information, this news release may contain
forward-looking statements that reflect the Company's current expectation
regarding future events. These forward-looking statements involve risk and
uncertainties, which may cause, but are not limited to, changing market
conditions, the successful and timely completion of clinical studies, the
establishment of corporate alliances, the impact of competitive products and
pricing, new product development, uncertainties related to the regulatory
approval process, and other risks detailed from time to time in the Company's
ongoing quarterly and annual reporting.

    %SEDAR: 00013159E




For further information:

For further information: Jennifer Shea, Vice-President, Communications,
Investor & Government Relations, Bioniche Life Sciences Inc., Telephone: (613)
966-8058, Cell: (613) 391-2097, Jennifer.Shea@Bioniche.com

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