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Applications for Temporary Assistance for Needy Families and food stamps have increased nationwide. The number of families, the Temporary Assistance for Needy Families to about 16 % compared with October 2007, the support of 2,900 Oregon families more than a year ago. Households, the food stamps increased by 13 %, for an additional workload of approximately 29,000 households.

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2009 Poniard Pharmaceuticals, Inc. All rights reserved.Poniard and Poniard Pharmaceuticals are registered trademarks of Poniard Pharmaceuticals,Poniard Pharmaceuticals,Poniard Pharmaceuticals, SCLC patients PARD), is a biopharmaceutical company on oncology, announced that he has reached his target accrual of from 400 patients in the SPEAR survey. This global phase 3 trial is evaluating efficacy and safety by picoplatin in patients with relapsed small cell lung front prior have failed platinum-based first-line chemotherapy or that progressed in six months from the first online therapeutic. The patient inscribed more than 100 sites in 16 countries in Europe, Americas and Asia. The completion of patient enrollment in our Phase 3 SPEAR study represents a important milestone for Poniard We are accomplished this prior to internal projections, keep us on schedule to complete your clinical information analysis of and begin the submission of of a rolling allows a New Drug Application New Drug Application to the U.S. Food and Drug Administration of picoplatin into SCLC this year, said Jerry McMahon Chairman and Chief Executive Officer Poniard. We think that, picoplatin survival benefit to SCLC patients progression-free survival a significant achievement for such aggressive tumor, that very few with FDA – approved medications offers. .

In addition to the Stage 3 SPEARHEAD clinical trial in SCLC Picoplatin be even in the two ongoing Phase 2 trial The initial evaluation of safety and efficacy of picoplatin patients with metastatic colorectal cancer , and the second to patients with castration of -resistant evaluated prostate cancer. Oral picoplatin is also evaluated in a Phase 1 trial in solid tumors.

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