AVAX Technologies to Present at Rodman & Renshaw Techvest 2nd Annual Global Healthcare Conference
2005年5月5日 - 3:01PM
ビジネスワイヤ(英語)
AVAX Technologies, Inc. (OTCMarket:AVXT.OB) today announced that it
will present at the Rodman & Renshaw Techvest 2nd Annual Global
Healthcare Conference in Paris, France at 12:20 PM CEST (6:20 am
EDT) on Thursday, May 5, 2005. Richard Rainey, President of AVAX
Technologies, will provide an update on the Company's corporate and
development programs. About AVAX Technologies, Inc. AVAX
Technologies, Inc. is a biotechnology company with operations in
the United States and Europe. The Company is engaged in the
research, clinical and commercial development of biological
products and cancer therapeutics. AVAX's AC Vaccine platform is a
therapeutic treatment for cancer. In addition, the Company performs
contract-manufacturing services for biological products to other
pharmaceutical and biotechnology companies. The AC Vaccines are
prepared by attaching a small chemical to the patients tumor cells
in a process known as haptenization. This hapten modification
allows the tumor cells to stimulate a T cell-based immune response
to a patients own tumor cells. An early indicator of T cell immune
activity is delayed type hypersensitivity (DTH). A previously
published article in the Journal of Clinical Oncology, February
2004 reported actual five-year survival data for a group of 214
patients with clinically evident Stage III melanoma treated with
the AC Vaccine following surgery. The study demonstrated five-year
survival of 45% and showed a highly statistically significant
relationship between survival and DTH to patients' own tumor cells.
Notably, based upon these results, DTH appears to be a viable
"surrogate marker" for survival and an early indicator for clinical
effectiveness of current and future product candidates. Previously
clinical trials in ovarian and renal cell carcinoma, demonstrated
strong DTH responses consistent with those reported for melanoma
patients. Except for statements that are historical, the statements
in this release are "forward-looking" statements that are made
pursuant to the safe harbor provisions of Section 27A of the
Securities Act of 1933 and Section 21E of the Securities Exchange
Act of 1934. Forward-looking statements involve significant risks
and uncertainties, and in light of the significant uncertainties
inherent in such statements, the inclusion of such information
should not be regarded as a representation by AVAX that the
objectives and plans of the Company will be achieved. In fact,
actual results could differ materially from those contemplated by
such forward-looking statements. Many important factors affect the
Company's prospects, including (1) receipt of the balance of the
funds from the private placement transaction and in the future to
obtain substantial additional funds, beyond the announced private
placement, (2) the results of clinical and laboratory testing of
its vaccine technologies, (3) possible future FDA or AFSSAPS
questions regarding the Company's products and manufacturing
processes, (4) the Company's ability to maintain its rights under
license agreements and to meet funding requirements under its
license agreements, (5) the Company's ability to demonstrate the
safety and efficacy of product candidates at each stage of
development and to meet applicable regulatory standards and receive
required regulatory approvals, as well as other risks detailed from
time to time in AVAX's public disclosure filings with the
Securities and Exchange Commission, including its prospectus
forming a part of the Company's registration statement on form SB-2
filed November 8, 2005 and its Annual Report on Form 10-KSB for the
year ended December 31, 2003. AVAX does not undertake any
obligation to release publicly any revisions to these
forward-looking statements or to reflect the occurrence of
unanticipated events.
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