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GPC Biotech Announces that Partner Pharmion Submits European Marketing
Application for Satraplatin    GPC Biotech AG (Frankfurt Stock Exchange:
GPC; TecDAX
index; Nasdaq: GPCB) today announced that its partner, Pharmion
Corporation
(Nasdaq: PHRM), has submitted a Marketing Authorization Application
(MAA)
to the European Medicines Agency (EMEA) for satraplatin in combination
with
prednisone for the treatment of patients with metastatic hormone
refractory
prostate cancer (HRPC) who have failed prior chemotherapy. This filing
is
based primarily on data from the SPARC Phase 3 registrational trial.
     "We are delighted that Pharmion has submitted the European marketing
application for satraplatin," said Bernd R. Seizinger, M.D., Ph.D.,
Chief
Executive Officer. "With over 60,000 people expected to die from
prostate
cancer in the European Union this year, there is an urgent need for new
therapies. We believe that, if approved, satraplatin has the potential
to
become an important new treatment option for advanced prostate cancer
patients who today have very little hope."
     GPC Biotech will receive an $8 million milestone payment from
Pharmion
in connection with EMEA's acceptance of this filing. Under the terms of
GPC
Biotech's agreement with Spectrum Pharmaceuticals, the acceptance of the
MAA by the EMEA will also trigger payments by GPC Biotech to Spectrum in
a
total amount of $3.2 million, representing a direct milestone payment
plus
Spectrum's share of the $8 million milestone payment from Pharmion.

AZhttp, Inc. <http://www.azhttp.com/>  Biotechnology Marketing 
<http://www.azhttp.com/2007/04/29/biotechnology/>  

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