Wyeth And Progenics Announce Preliminary Clinical Trial Results For RELISTOR Oral And Intravenous Formulations

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Rifampin and saquinavir should not be taken in negotiation beside NORVIR. Patients should describe their surgeon if they be taking rifampin and saquinavir.

RELISTOR Oral Formulation The study of the RELISTOR oral formulation be a double-blind, randomized, placebo-controlled phase 2 trial. In this four-week trial of 122 patients with chronic, non-malignant pain (such by means of stern pain, neuropathic pain or osteoarthritis) who be unloading opioids for pain headship, the once each afternoon oral formulation of RELISTOR showed statistically decisive activity as assess by means of the commonness of out of the blue bowel drills and other efficacy measures. This oral formulation was also shown to be across the world resourcefully tolerate.

"We be enchanted by the opening findings of this oral formulation" right to be heard Paul J. Maddon, M.D., Ph.D., Founder, Chief Executive Officer and Chief Science Officer of Progenics Pharmaceuticals, Inc. "We await grades within the coming months from a second, ongoing phase 2 study involving the oral formulation of RELISTOR that was announced finishing July to hold positive activity in a phase 1 trial." RELISTOR Intravenous Formulation The Progenics-conducted phase 3 study of an intravenous formulation of RELISTOR for patients with post-operative ileus (POI) did not meet the primary or secondary end points, confirm the closer findings of the Wyeth phase 3 intravenous POI study announced next to March 12, 2008. Progenics and Wyeth will immensely right now study the results of both phase 3 intravenous POI studies to make certain whether and how to carry on expansion of this formulation of RELISTOR and this confirmation.

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