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3SBio Inc. Announces Second Quarter 2008 Results
Date:8/12/2008

ompany and shareholder value.

Phase III Program Updates

High-dosage EPIAO

We have completed the full analysis of the Phase III trial to evaluate the safety and efficacy of a weekly subcutaneous injection of 36,000 IU EPIAO in oncology patients compared with a regimen of three times per week administration of 10,000 IU EPIAO. The results show that 70% of patients on high-dose EPIAO injections had Hemoglobin improvement of 1-2 mg/dl from baseline, similar to those on three times per week dosing of 10,000 IU EPIAO. More importantly, the weekly administration of 36,000 IU EPIAO demonstrated equivalent safety and tolerability profile as a three times per week 10,000 IU EPIAO. We remain on track to file with the SFDA in the third quarter of 2008. Pending approval by the SFDA, the once-weekly EPIAO will improve compliance for both existing and new patients as a result of greater convenience given the reduction in the number of injections required.

NuLeusin

Preliminary results from the analysis of the Phase III clinical trial data for NuLeusin (our second generation IL-2), completed in the first quarter 2008, demonstrated 11% partial response, with one patient registering a complete response. We are on track to file application for approval during the second half of 2008. Upon approval by the SFDA, we believe NuLeusin could be the first product of its kind for the treatment of late stage renal carcinoma available in China, and would provide an important treatment for late stage renal cancer patients who have exhausted other treatment options.

TPIAO for ITP

We have achieved our enrollment goal for the Phase III trial for TPIAO for the treatment of idiopathic thrombocytopenic purpura (ITP). We remain on track to file the application for approval with the SFDA in the fourth quarter of 2008.

TPIAO Phase IV Studies

To maximize the commercial potential and to ensure the continued long term growth of TPIAO, we initiate
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SOURCE 3SBio Inc.
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