February 17, 2006
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Santen reports interim results with two new glaucoma drugs

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Preliminary results from clinical trials of two glaucoma drug candidates, an angiotensin-2 receptor antagonist and a prostaglandin derivative, have shown mixed results, Santen Pharmaceuticals said in a press release.

An early phase 2 study of DE-092, also known as olmesartan, in the United States indicated “some IOP reduction,” the company said, but the efficacy was insufficient, and no clear dose-response relationship was seen among the various concentrations. Santen is considering another dose-response study and may reposition DE-092 in the United States and Europe after the Japanese phase 2 results are available, the release said. Santen is conducting a late phase 2 trial of the compound in Japan.

A phase 3 trial of DE-085, also known as tafluprost, in Europe has “demonstrated DE-085’s strong IOP-lowering effect as expected for prostaglandins, but the drug did not demonstrate non-inferiority to latanoprost for the primary endpoint,” the company said. The study is ongoing, and Santen plans to conduct a detailed analysis once final results are available.