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Summary for Generic Name: thalidomide
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Clinical Trials for: thalidomidePreoperative Thalidomide With Radiation Therapy For Patients With Low-Grade Primary Soft Tissue Sarcoma or Thalidomide With Radiation Therapy and Chemotherapy For Patients With High-Grade or Intermediate-Grade Primary Soft Tissue Sarcoma of the Arm, Leg, or Body Wall Status: Completed Condition: Recurrent Adult Soft Tissue Sarcoma; Stage I Adult Soft Tissue Sarcoma; Stage II Adult Soft Tissue Sarcoma; Stage III Adult Soft Tissue Sarcoma Phase II Trial of Thalidomide Combined With Concurrent Chemoradiotherapy in Esophageal Cancer Status: Recruiting Condition: Esophageal Cancer Irinotecan and Thalidomide in Treating Patients With Advanced Solid Tumors Status: Completed Condition: Unspecified Adult Solid Tumor, Protocol Specific Iberoamerican Protocol With Thalidomide in Patients With Symptomatic Newly Diagnosed Multiple Myeloma Over 65 Years Status: Active, not recruiting Condition: Multiple Myeloma Thalidomide Plus Dexamethasone as Maintenance Therapy for Multiple Myeloma Status: Completed Condition: Multiple Myeloma Long-term Effects of Thalidomide for Recurrent Gastrointestinal Bleeding Due to Vascular Malformation Status: Completed Condition: Obscure Gastrointestinal Bleeding; Angiodysplasia; Gastric Antral Vascular Ectasia; Thalidomide TT II: Multiple Myeloma Evaluating Anti-Angiogenesis With Thalidomide and Post-Transplant Consolidation Chemotherapy Status: Active, not recruiting Condition: Multiple Myeloma Thalidomide With or Without Fludarabine in Treating Patients With Hematologic Cancer Status: Completed Condition: Recurrent Small Lymphocytic Lymphoma; Refractory Chronic Lymphocytic Leukemia Thalidomide for the Treatment of Hormone-Dependent Prostate Cancer Status: Completed Condition: Prostate Cancer GEM05 for Patients With Multiple Myeloma Under 65 Years Status: Completed Condition: Multiple Myeloma 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 | Patented / Exclusive Use | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Celgene | THALOMID | thalidomide | CAPSULE; ORAL | 020785 | Jul 16, 1998 | RX | No | <disabled> | ORPHAN DRUG EXCLUSIVITY | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Celgene | THALOMID | thalidomide | CAPSULE; ORAL | 020785 | Jul 16, 1998 | RX | No | 6,561,977 | <disabled> | APPROVAL FOR MARKETING ONLY UNDER A SPECIAL RESTRICTION PROGRAM APPROVED BY FDA CALLED "SYSTEM FOR THALIDOMIDE EDUCATION AND PRESCRIBING SAFETY" (S.T.E.P.S.) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Celgene | THALOMID | thalidomide | CAPSULE; ORAL | 020785 | Jul 16, 1998 | RX | No | 6,908,432 | <disabled> | APPROVAL FOR MARKETING ONLY UNDER A SPECIAL RESTRICTION PROGRAM APPROVED BY FDA CALLED "SYSTEM FOR THALIDOMIDE EDUCATION AND PRESCRIBING SAFETY" (S.T.E.P.S.) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Celgene | THALOMID | thalidomide | CAPSULE; ORAL | 020785 | Jul 16, 1998 | RX | No | 6,869,399 | <disabled> | MAINTENANCE THERAPY FOR PREVENTION AND SUPRESSION OF THE CUTANEOUS MANIFESTATIONS OF ENL RECURRENCE | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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