Articles tagged with: Daratumumab
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During the upcoming annual meeting of the American Society of Clinical Oncology (ASCO), results will be presented from clinical trials involving potential new drugs under development for the treatment of multiple myeloma.
In particular, results for newer, lesser known agents that are in the early stages of clinical development will take center stage. These agents include obatoclax, siltuximab, daratumumab, and SNS01-T.
According to the recently released ASCO abstracts, the agents showed varying degrees of activity in relapsed and refractory myeloma patients. So it will be particularly interesting to …
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The 48th annual meeting of the American Society of Clinical Oncology (ASCO) will take place Friday, June 1, through Tuesday, June 5, in Chicago.
More than 25,000 clinical specialists from all over the world are expected to attend the five-day meeting to discuss the current research in cancer treatment and care. The theme for this year’s meeting is “Collaborating to Conquer Cancer.”
The meeting will include many presentations and seminars focused specifically on multiple myeloma. The ASCO website currently lists nearly 50 myeloma-based presentations (included under “lymphoma and plasma cell disorders”).
The …
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Celgene Seeks Expanded Approval For Revlimid In Europe – The pharmaceutical company Celgene announced on Tuesday that it is seeking expanded approval for Revlimid (lenalidomide) as treatment for multiple myeloma in Europe. The European Medicines Agency (EMA) will review approval of Revlimid for maintenance therapy of newly diagnosed myeloma patients who have not progressed after initial therapy with melphalan (Alkeran), prednisone, and Revlimid or after autologous stem cell transplantation. Currently, Revlimid is approved in combination with dexamethasone for the treatment of patients who have received at least one prior therapy. For more information, please see the Celgene press release.
ENMD-2076 Is Safe In Relapsed/Refractory Multiple Myeloma (ASH 2010) – The investigational drug ENMD-2076, which is being developed by the pharmaceutical company EntreMed, is safe in relapsed / refractory multiple myeloma patients, according to the interim Phase 1 trial results presented at the 2010 Meeting of the American Society of Hematology (ASH). Researchers tested four different dose levels (150 mg to 400 mg) in 28-day cycles. They observed progression of disease for all patients receiving the minimum dose of 150 mg. Patients receiving a dose of 300 mg achieved stable disease with reductions in serum M-protein. Researchers did not observe any dose-limiting side effects. Most side effects were mild to moderate and included nausea, diarrhea, and fatigue. The optimal dosage has not yet been determined as the trial is still ongoing. For more information, please see abstract 1957 on the ASH annual meeting website and the clinical trial description.
Daratumumab Emerges As Potential Treatment In CD38-Positive Multiple Myeloma – Preclinical results showed that the experimental drug daratumumab is highly effective at killing cancerous cells that produce the CD38 molecule. The Danish biotechnology company Genmab is currently developing daratumumab for treatment of CD38-positive multiple myeloma tumors. Researchers initially tested a broad array of CD38 antibodies against more than 10 primary tumors from myeloma patients, and daratumumab was found to be the most effective at executing the immune system killing mechanisms. Genmab is currently conducting a Phase 1/2 study to determine the safety and optimal dosage of daratumumab. For more information, please see the study in the Journal of Immunology (abstract) and the clinical trial description.
PBOX-15 Induces Cell Death In Multiple Myeloma Cells – Preclinical results demonstrated that the experimental drug compound PBOX-15 (1,5-benzoxazepine-15), discovered by Irish clinical scientists, is a promising treatment for multiple myeloma. Researchers found that PBOX-15 induced cell death in four different lines of multiple myeloma cells. In two of the cell lines, PBOX-15 increased the number of death receptor genes to stimulate cell death. For more information, please see the study in the British Journal of Cancer (abstract).