ooking statements, which
express the current beliefs and expectations of the management of
GPC Biotech AG and Pharmion Corporation, including statements
relating to results of the SPARC trial and statements relating to
the potential efficacy and safety profile of satraplatin. Such
statements are based on current expectations and are subject to
risks and uncertainties, many of which are beyond our control, that
could cause future results, performance or achievements to differ
significantly from the results, performance or achievements
expressed or implied by such forward-looking statements. Actual
results could differ materially depending on a number of factors,
and we caution investors not to place undue reliance on the
forward-looking statements contained in this press release. In
particular, there can be no guarantee that additional information
relating to the safety, efficacy or tolerability of satraplatin may
be discovered upon further analysis of data from the SPARC trial or
analysis of additional data from other ongoing clinical trials for
satraplatin. Furthermore, we cannot guarantee that satraplatin will
be approved for marketing in a timely manner, if at all, by
regulatory authorities nor that, if marketed, satraplatin will be a
successful commercial product. We direct you to GPC Biotech's
Annual Report on Form 20-F for the fiscal year ended December 31,
2005, Pharmion's Quarterly Report on Form 10-Q for the quarterly
period ended March 31, 2007, its Annual Report on Form 10-K for the
fiscal year ended December 31, 2006, and other reports filed with
the U.S. Securities and Exchange Commission for additional details
on the important factors that may affect the future results,
performance and achievements of either Pharmion or GPC Biotech.
Forward-looking statements speak only as of the date on which they
are made and neither Pharmion nor GPC Biotech undertakes any
obligation to update these forward-looking statements, even if new
information becomes availabl
'"/>Page: 1 2 3 4 5 6 7 Related medicine technology :1.
Portola Pharmaceuticals Announces Positive Phase II EXPERT Results
and Additional Oral and Poster Presentations at the XXI Congress of
the International Society on Thrombosis and Haemostasis (ISTH)2.
Cytokinetics Reports Additional Clinical Trials Data for Ispinesib3.
Additional Data on CombinatoRx Drug Candidates CRx-102 and CRx-139
Presented at EULAR4.
Further Statistical Analysis of the Recent Phase III trial on Lead
Product M6G Shows Additional Benefits5.
Novel Mechanism Insights and Additional Data on CombinatoRx Drug
Candidates to Be Presented at Upcoming EULAR Meeting6.
Elixir Pharmaceuticals Presents Additional Preclinical Data
Demonstrating the Potential of Ghrelin Antagonism to Regulate
Metabolism, Body Weight and Glycemic Control7.
Cell Genesys Reports Additional Data From Phase 2 Clinical Trial of
GVAX Immunotherapy for Pancreatic Cancer8.
Additional New Data from Satraplatin SPARC Phase 3 Investigational
Trial Presented at ASCO Annual Meeting9.
New Study Results Provide Additional Data about Short- and
Long-Term Use of Desvenlafaxine Succinate in the Treatment of
Adults with Major Depressive Disorder10.
Additional Efficacy Data from Satraplatin SPARC Phase 3
Investigational Trial Presented at Annual Meeting of American
Urological Association11.
PTC Therapeutics Announces Additional Positive Interim Phase 2
Results of PTC124 in Duchenne Muscular Dystrophy