cacy in subsequent clinical trials, the risk
that encouraging results from early research, preclinical studies or
clinical trials may not be confirmed upon further analysis of the detailed
results of such research, preclinical study or clinical trial, the risk
that additional information relating to the safety, efficacy or
tolerability of our product candidates may be discovered upon further
analysis of preclinical or clinical trial data, the risk that we or our
collaborators will not obtain approval to market our product candidates,
and the risks associated with reliance on collaborators, including
MedImmune, Merck Serono, TRACON and Nycomed, for the funding or conduct of
further development and commercialization activities relating to our
product candidates. These factors and others are more fully discussed in
our Annual Report on Form 10-K for the fiscal year ended December 31, 2007,
filed with the SEC on March 14, 2008, as well as other filings by the
company with the SEC.
Any forward-looking statements are made pursuant to Section 27A of the
Securities Act of 1933, as amended, and Section 21E of the Securities
Exchange Act of 1934, as amended, and, as such, speak only as of the date
made. Micromet undertakes no obligation to publicly update any
forward-looking statements, whether as a result of new information, future
events or otherwise.
Micromet, Inc.
Condensed Consolidated Balance Sheets
(In thousands, except par value)
March 31, December 31,
2008 2007
Assets
Current assets:
Cash and cash equivalents $27,653 $27,066
Accounts receivable 1,734 4,689
Prepaid expenses and other current assets 1,658 2,579
Total current ass
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