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Summary for Tradename: RAPAMUNE
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Clinical Trials for: RAPAMUNEProspective Study of Rapamycin for the Treatment of SLE Status: Recruiting Condition: Systemic Lupus Erythematosus (SLE) Study of RAD001 (Everolimus) for Children With NF1 and Chemotherapy-Refractory Radiographic Progressive Low Grade Gliomas Status: Recruiting Condition: Glioma Dose Finding Study of RAD001 (Everolimus, Afinitor®) in Combination With BEZ235 in Patients With Advanced Solid Tumors Status: Recruiting Condition: Advanced Solid Tumors; Metastatic Breast Cancer; Metastatic Renal Cell Carcinoma Vemurafenib in Combination With Everolimus or Temsirolimus With Advanced Cancer Status: Recruiting Condition: Advanced Cancer; Solid Tumor A Study of the mTOR Inhibitor Rapamycin (Rapamune, Sirolimus) in Combination With Abraxane in Advanced Solid Cancers Status: Recruiting Condition: Advanced Solid Cancers Everolimus (RAD001) in Metastatic Transitional Cell Carcinoma of the Urothelium Status: Active, not recruiting Condition: Bladder Cancer; Metastatic Transitional Cell Carcinoma A Pilot Study Evaluating the Use of mTor Inhibitor Sirolimus in Children and Young Adults With Desmoid-Type Fibromatosis Status: Terminated Condition: Desmoid Tumor RAD001 (Everolimus) + Docetaxel + Cisplatin as Induction Chemotherapy in Patients With Local-Regional Advanced Head and Neck Cancer Status: Active, not recruiting Condition: HEAD & NECK Cancer BNC105P in Combination With Everolimus/Following Everolimus For Progressive Metastatic Clear Cell Renal Cell Carcinoma Status: Recruiting Condition: Renal Cell Carcinoma Everolimus (RAD001) in Primary Therapy of Waldenstrom's Macroglobulinemia Status: Active, not recruiting Condition: Waldenstrom's Macroglobulinemia Courtesy of ClinicalTrials.org See more clinical trials for this drug | ||||||||
| Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | Type | RLD | Patent No. | Product | Substance | Delist_Flag | Patent Expiration | Exclusivity Expiration | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Wyeth Pharms Inc | RAPAMUNE | sirolimus | SOLUTION; ORAL | 021083 | Sep 15, 1999 | RX | Yes | 5,100,899*PED | Y | <disabled> | <disabled> | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Wyeth Pharms Inc | RAPAMUNE | sirolimus | SOLUTION; ORAL | 021083 | Sep 15, 1999 | RX | Yes | 5,403,833*PED | <disabled> | <disabled> | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Wyeth Pharms Inc | RAPAMUNE | sirolimus | SOLUTION; ORAL | 021083 | Sep 15, 1999 | RX | Yes | 5,536,729*PED | Y | <disabled> | <disabled> | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Wyeth Pharms Inc | RAPAMUNE | sirolimus | TABLET; ORAL | 021110 | Aug 22, 2002 | RX | Yes | 5,100,899*PED | Y | <disabled> | <disabled> | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Drugname | Dosage | Strength | RLD | Submissiondate |
| sirolimus | Tablets | 0.5 mg | Rapamune | 8/25/2010 |
| sirolimus | Tablets | 1 mg and 2 mg | Rapamune | 12/17/2009 |
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