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Feb 4
New Dosing Recommendations for RAPAMUNE® (sirolimus) in High Immunologic Risk Renal Transplant Patients, Approved by the USFDA
Wyeth Pharmaceuticals’ immunosuppressant drug RAPAMUNE® (sirolimus) has been approved by the USFDA of its new dosing recommendations.

RAPAMUNE® is the first and only kidney transplant therapeutic with dosing recommendations specifically for the treatment of high immunologic risk renal transplant recipients.

In high immunologic risk patients, it is recommended that a RAPAMUNE-based regimen be used in combination with cyclosporine (CsA) and corticosteroids for the first year following transplantation.

rapamune.jpgNow, with the newly approved dosing recommendation, RAPAMUNE® can be used in combination with antibody induction therapy in high immunologic risk kidney transplant patients.

This particular patient population have a greater likelihood of developing acute rejection than low to moderate risk kidney transplant recipients.

High immunologic risk patients are defined as transplant recipients who are Black; and/or repeat renal transplant recipients who lost a previous kidney transplant for immunologic reasons; and/or patients with high-panel reactive antibodies (PRA). For patients with high PRA, it is more difficult to find a compatible organ donor.

RAPAMUNE® (sirolimus) belongs to a novel class of immunosuppressant agents called mammalian target of rapamycin (mTOR) inhibitors, a key regulatory enzyme involved in cell growth and survival.

Wyeth Pharmaceuticals, Inc. (10944776) is a division of Wyeth (NYSE: WYE).

Source: Wyeth News

[Photo Credit: Wyeth Pharmaceuticals]


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« Anacor Signed Worldwide Exclusive License Agreement with Schering-Plough for New Topical Anti-Fungal, AN2690 | Main | Genentech’s Raptiva® (efalizumab) Passed Phase IV Study in Moderate-to-Severe Hand and Foot Psoriasis Patients »

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