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To: bigbuk who wrote (131597)4/21/2004 2:13:59 PM
From: StocksDATsoar  Respond to of 150070
 
YUP, DUMP A.S.A.P

U THINK SEC SCREWED UP?

COMTEX) B: Biocurex Tells SEC, 'Let's Talk,' Stands By Its Press Releases
B: Biocurex Tells SEC, 'Let's Talk,' Stands By Its Press Releases Following Susp

Apr 19, 2004 (financialwire.net via COMTEX) -- (FinancialWire) Biocurex Inc.
(OTCBB: BOCX; OTC: BOCX) may be temporarily suspended from trading but it
doesn't seem suspended from talking or taking issue with the U.S. Securities and
Exchange Commission charges.

The company's shares were temporarily suspended due to "questions regarding the
accuracy of assertions by Biocurex and others, in press releases and e-mails to
investors concerning, among other things, (1) a study confirming the
effectiveness of its primary product and (2) approval of its main product by the
Food and Drug Administration."

Biocurex said it has "notified the SEC that it is eager to answer any
questions the SEC may have regarding these issues and is presently awaiting a
response from the SEC on this matter," and that "Biocurex is not
responsible for the unauthorized circulation of corporate material 'by others',
nor any material that could be construed as misleading to investors or outright
erroneous in its content."

The company also said that the U.S. Food and Drug Administration has classified
Biocurex's Histo-RECAF(TM) as a Class I device under Regulation Number 864.1850,
Code HZJ owned by BioCurex (FDA number 9046509). Thus, the product is available
as a "Staining test for AFP receptors (a.k.a. RECAF) in tissues" for sale to
pathology laboratories across the USA, and that the company "firmly stands
by the results announced in its April 5, 2004 press release and by its RECAF
technology in general."

Friday, Biocurex stated that Protokinetix announced preliminary results from a
study carried out by the George Pompidou Hospital in France which was designed
to validate the Company's Histo-RECAF(TM) version 2.0. This version uses a high
affinity anti-RECAF antibody which improves the contrast between cancer cells
and the surrounding non-malignant tissue.

"The study was commissioned by Protokinetix Inc., which was granted a
license by BioCurex to commercialize therapeutic anti-RECAF antibodies modified
according to Protokinetix's Super-Antibody proprietary technology and the
Perigene (Compiegne, France) catalytic antibody technology," a company press
release noted.

It quoted Dr. Jean-Marie Dupuis, a scientist involved with the Pompidou
validation study, as describing the results obtained with BioCurex kits as 'very
positive' and stating that "the labeling of the malignant cells is strong and
clear with a nice delineation between malignant and normal cells."

CEO Dr. Ricardo Moro stated: "We are very pleased with these very preliminary
results, which validate our claims at a time in which our technology is under
scrutiny.

"The findings are very significant because the study is being carried out by an
extremely reputable institution. The results are also important to us because
the study uses our new anti-RECAF antibody which works significantly better than
the former reagent in the kit.

"We are looking forward to the final conclusions of this study. We expect that
the Pompidou analysis will continue to confirm the positive results we have
obtained in our own research facilities. Moreover, we are excited about the
potential of combining the Super-Antibody and the Catalytic-Antibody
technologies with our own RECAF(TM) technology.

"BioCurex has pending patents for a number of cancer therapy applications using
RECAF(TM). These applications cover conjugates between anti-RECAF antibodies
with a variety of drugs, radio-isotopes and a cancer vaccine."

He said that this second version of Histo-RECAF being tested by the Pompidou
group has not been yet submitted to the FDA.

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