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PDL BioPharma Announces Long-Term Nuvion Data Presented at 2007,Digestive Disease Week

ion in this press release should be considered accurate only as of the date of this press release. PDL has no intention of updating and specifically disclaims any duty to update the information in this press release for any reason, except as required by law, even as new information becomes available or other events occur in the future. This press release contains "forward-looking statements" that are based on current expectations and assumptions that are subject to risks and uncertainties. The actual results may differ materially from those in the forward-looking statements because of various factors, risks and uncertainties. In particular, results obtained in the Phase 1 and Phase 1/2 studies of the Nuvion (visilizumab) antibody may not be predictive of results that may be obtained in the additional evaluations that would be necessary to demonstrate visilizumab to be safe and effective in the treatment of IVSR-UC, nor can there be assurance that PDL will initiate or complete the subsequent clinical trials and evaluations that would be necessary to support marketing approval of the Nuvion antibody by the United States Food and Drug Administration. For further information regarding factors, risks and uncertainties that may cause such differences, please refer to the filings PDL has made with the Securities and Exchange Commission, including the "Risk Factors" sections of PDL's Quarterly and Annual Reports, copies of which may be obtained at the "Investors" section on PDL's website at www.pdl.com. All forward-looking statements in this press release are qualified in their entirety by this cautionary statement.

NOTE: PDL BioPharma and the PDL BioPharma logo are considered trademarks of PDL BioPharma, Inc. Nuvion is a registered U.S. trademark of PDL BioPharma, Inc.

CONTACT: Jean Suzuki, Investor Relations, +1-510-574-1550,; or Kathleen Rinehart, Corporate Communications,+1-510- 574-1480, , both of PDL BioP
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