| Subject: | FDA Informs of New Clinical Trial Results for Sirolimus (marketed as Rapamune) |
| Category: | Food and Drug Administration (FDA)
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| Published: | Thu, 11 Jun 2009 - 11:00 am |
| The FDA is notifying healthcare professionals of clinical trial data that suggest increased mortality in stable liver transplant patients after conversion from a calcineurin inhibitor (CNI)-based immunosuppressive regimen to sirolimus (Rapamune). The trial was conducted by sirolimus manufacturer, Wyeth. The Agency will continue to examine the data on mortality and other adverse events in this study, and will make further recommendations, as appropriate. At this time the FDA is determining... The full article is available to StayAlert subscribers. Click here for a free trial subscription. |
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