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Genentech, Inc., a wholly–owned member of the Roche Group, announced that the Phase III study CRUISE showed Lucentis improved vision, as measured by the primary endpoint of mean change from baseline in best–corrected visual acuity at six months, in patients with macular edema due to central retinal vein occlusion. The safety profile of Lucentis was consistent with previous experience and no new adverse events related to Lucentis were observed in the study.

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