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Biopure to Apply for European Marketing Approval of Hemopure(R) in 2006

    CAMBRIDGE, Mass., Jan. 11 /PRNewswire-FirstCall/ -- Biopure Corporation
(Nasdaq: BPUR) announced today that it plans to apply in mid 2006 for
regulatory approval to market its investigational oxygen therapeutic
Hemopure(R) [hemoglobin glutamer - 250 (bovine)] in Europe for the treatment
of acute anemia in elective orthopedic surgery patients.
    "This planned submission will be our first marketing application in Europe
and will incorporate the considerable work we've been doing to address the
Food and Drug Administration's questions regarding our previous U.S. marketing
application for this orthopedic surgery indication," said Biopure President
and CEO Zafiris G. Zafirelis.  "We intend to use existing data and new
analyses of our two completed Phase 3 surgery trials to support the product's
risk-benefit profile in this indication in Europe.  We're currently preparing
the European application and are continuing with our previously announced
development plan for Hemopure in cardiovascular ischemia and out-of-hospital
trauma."
    The European Agency for the Evaluation of Medicinal Products (EMEA) has
notified Biopure that Hemopure is eligible for submission of a marketing
application through the European Union's centralized filing procedure for all
25 member states.  In December 2005, the company began meeting with regulatory
authorities of individual countries to assess whether to apply through the
centralized or decentralized E.U. procedure and to determine which countries
would be most appropriate for an orthopedic surgery indication.  Prior to each
meeting, the company provides a summary of an application for discussion of
the proposed indication as well as other potential future indications.
Biopure is also considering submitting the marketing application to non-E.U.
countries in Europe.  The product's approvability will only be assessed once a
complete marketing application has been formally submitted for review.
    The clinical section of Biopure's application will include data from a
688-patient Phase 3 orthopedic surgery trial conducted in the United States,
South Africa, Europe and Canada, and from a 160-patient Phase 3 general non-
cardiac surgery trial conducted in South Africa and Europe.

    Surgical Anemia
    Anemia is a deficiency of red blood cells in the bloodstream caused by
blood loss (e.g., from surgery or injury) or other disorders, which can
compromise the body's oxygen-carrying capacity and in severe cases lead to
cell damage, organ dysfunction or death.  Hemoglobin is a protein normally
contained within red blood cells that carries and releases oxygen to the
body's tissues.
    Hemopure is an oxygen therapeutic, or oxygen-carrying biologic drug,
consisting of stabilized bovine hemoglobin formulated in a balanced salt
solution.  These polymerized (chemically cross-linked) hemoglobin molecules
circulate in the plasma (the fluid part of blood) when infused and are
smaller, less viscous and more readily release oxygen to tissues than red
blood cells.  Hemopure is ultrapurified, compatible with all blood types, and
stable for three years without refrigeration.

    About Biopure Corporation
    Biopure Corporation develops, manufactures and markets pharmaceuticals,
called oxygen therapeutics, that are intravenously administered to deliver
oxygen to the body's tissues. The company is developing Hemopure(R)
[hemoglobin glutamer - 250 (bovine)], or HBOC-201, for a potential indication
in cardiovascular ischemia and, in collaboration with the U.S. Naval Medical
Research Center, for a potential out-of-hospital trauma indication. The
product is approved in South Africa for the treatment of surgery patients who
are acutely anemic and for eliminating, delaying or reducing allogenic red
blood cell transfusions in these patients. Hemopure has not been approved for
sale in other jurisdictions, including the U.S. or the European Union.
Biopure's veterinary product Oxyglobin(R) [hemoglobin glutamer - 200
(bovine)], or HBOC-301, the only oxygen therapeutic approved by the U.S. Food
and Drug Administration and the European Commission, is indicated for the
treatment of anemia in dogs.
    On January 11, 2006, Biopure commenced a public offering of its common
stock and warrants to which this communication is deemed to relate.  Biopure
has filed a registration statement (including a prospectus) with the
Securities and Exchange Commission for that offering.  Before you invest, you
should read the prospectus in that registration statement and other documents
the issuer has filed with the SEC for more complete information about the
issuer and this offering.  You may get these documents for free by visiting
EDGAR on the SEC Web site at http://www.sec.gov.  Alternatively, Biopure, any
underwriter or any dealer participating the offering will arrange to send you
the prospectus if you request it by calling toll-free 1-866-928-0928.

    Statements in this press release that are not strictly historical are
forward-looking statements, including those that relate to the timing of the
planned application to market Hemopure in Europe and those that imply that
Biopure may obtain marketing approval of Hemopure in Europe.  Actual results
may differ materially from those projected in these forward-looking statements
due to risks and uncertainties.  These risks include, without limitation,
uncertainties regarding the company's financial position, unexpected costs and
expenses, determinations by European, U.S. or other regulatory authorities,
unanticipated problems with the product's commercial use, whether or not
product related, and with product distributors, sales agents or other third
parties, delays in or unpredictable outcomes of clinical trials, and those
found in the company's filings with the U.S. Securities and Exchange
Commission, including under the heading "Risk Factors" in the Form 10-Q filed
on September 9, 2005, which can be accessed in the EDGAR database at the SEC
Web site, http://www.sec.gov.  The company undertakes no obligation to release
publicly the results of any revisions to these forward-looking statements to
reflect events or circumstances arising after the date hereof.  The content of
this press release does not necessarily reflect the position or the policy of
the U.S. Government or the Department of Defense, and no official endorsement
should be inferred.

    Contact: Douglas Sayles            Herb Lanzet (Investors)
             Biopure Corporation       H.L. Lanzet Inc.
             (617) 234-6826            (212) 888-4570
             IR@biopure.com            lanzet@aol.com


SOURCE Biopure Corporation




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    CONTACT:
    Douglas Sayles of Biopure Corporation,
    +1-617-234-6826, IR@biopure.com; Investors - Herb Lanzet of H.L.
    Lanzet Inc., +1-212-888-4570, lanzet@aol.com