CLINICAL TRIALS PROFILE FOR LENALIDOMIDE
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505(b)(2) Clinical Trials for LENALIDOMIDE
Trial Type | Trial ID | Title | Status | Sponsor | Phase | Start Date | Summary |
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New Combination | NCT00974233 ↗ | Study of Bendamustine/Rituxan Induction Chemotherapy With Revlimid Maintenance for Relapsed/Refractory CLL and SLL | Completed | Celgene Corporation | Phase 2 | 2009-10-01 | The purpose of this research is to evaluate a new combination of chemotherapy drugs for CLL/SLL using the drugs bendamustine (an intravenous chemotherapy drug), rituximab (an intravenous medication called a monoclonal antibody), and lenalidomide (an anti-cancer pill). The purpose of this study is to see if giving the chemotherapy pill lenalidomide after treatment with bendamustine and rituximab is able to prolong the period of time before the cancer starts growing again and causing symptoms. |
New Combination | NCT00974233 ↗ | Study of Bendamustine/Rituxan Induction Chemotherapy With Revlimid Maintenance for Relapsed/Refractory CLL and SLL | Completed | University of Wisconsin, Madison | Phase 2 | 2009-10-01 | The purpose of this research is to evaluate a new combination of chemotherapy drugs for CLL/SLL using the drugs bendamustine (an intravenous chemotherapy drug), rituximab (an intravenous medication called a monoclonal antibody), and lenalidomide (an anti-cancer pill). The purpose of this study is to see if giving the chemotherapy pill lenalidomide after treatment with bendamustine and rituximab is able to prolong the period of time before the cancer starts growing again and causing symptoms. |
New Combination | NCT01245673 ↗ | Combination Immunotherapy and Autologous Stem Cell Transplantation for Myeloma | Completed | University of Pennsylvania | Phase 2 | 2011-05-10 | One purpose of this study is to find out if a new combination of immune system treatments (MAGE-A3 vaccine plus activated T-cells) will allow the body to build up protection ("immunity") against the myeloma cells. A second purpose is to find out how well this combination of immune system treatments is able to control the myeloma. |
>Trial Type | >Trial ID | >Title | >Status | >Sponsor | >Phase | >Start Date | >Summary |
All Clinical Trials for LENALIDOMIDE
Trial ID | Title | Status | Sponsor | Phase | Start Date | Summary |
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NCT00031941 ↗ | CC-5013 in Treating Patients With Cancer That Has Not Responded to Previous Therapy | Completed | National Cancer Institute (NCI) | Phase 1 | 2002-04-01 | RATIONALE: CC-5013 may stop the growth of cancer by stopping blood flow to the tumor. PURPOSE: Phase I trial to study the effectiveness of CC-5013 in treating patients who have solid tumors and/or lymphoma that did not respond to previous therapy. |
NCT00031941 ↗ | CC-5013 in Treating Patients With Cancer That Has Not Responded to Previous Therapy | Completed | National Institutes of Health Clinical Center (CC) | Phase 1 | 2002-04-01 | RATIONALE: CC-5013 may stop the growth of cancer by stopping blood flow to the tumor. PURPOSE: Phase I trial to study the effectiveness of CC-5013 in treating patients who have solid tumors and/or lymphoma that did not respond to previous therapy. |
NCT00036894 ↗ | CC-5013 in Treating Patients With Recurrent Glioma | Completed | National Cancer Institute (NCI) | Phase 1 | 2002-03-01 | RATIONALE: CC-5013 may stop the growth of gliomas by stopping blood flow to the tumor. PURPOSE: Phase I trial to study the effectiveness of CC-5013 in treating patients who have recurrent glioma. |
>Trial ID | >Title | >Status | >Sponsor | >Phase | >Start Date | >Summary |
Clinical Trial Conditions for LENALIDOMIDE
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Clinical Trial Locations for LENALIDOMIDE
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Clinical Trial Progress for LENALIDOMIDE
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Clinical Trial Sponsors for LENALIDOMIDE
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