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|Articles|March 9, 2011

Oncology & Biotech News

  • December 2010
  • Volume 4
  • Issue 12

FDA Approves Zactima

Author(s)OBTN

An FDA advisory panel voted 10 to 0 in favor of approving Zactima (vandetanib) for patients with medullary thyroid cancer who have symptomatic, progressive disease.

An FDA advisory panel voted 10 to 0 in favor of approving Zactima (vandetanib) for patients with medullary thyroid cancer who have symptomatic, progressive disease. The panel expressed concerns about “substantial” drug-related toxicity associated with the 300-mg daily dose. Members said that patients taking Zactima appeared to be at greater risk for stroke and other cerebrovascular events and a prolonged QT interval.

Articles in this issue

almost 15 years ago

Medulloblastoma Subtypes Are Different Diseases

almost 15 years ago

ASH 2010: CPX-351 Improves Response in Elderly Patients With Newly Diagnosed Acute Myeloid Leukemia

almost 15 years ago

ASH 2010: Elotuzumab Highly Active in Patients With Advanced Myeloma

almost 15 years ago

ASH 2010: Intensified R-ACVBP More Effective and More Toxic Than R-CHOP in Diffuse Large B-Cell Lymphoma

almost 15 years ago

ASH 2010: Carfilzomib Shrinks Tumors in More Than One-Third of Pretreated Myeloma Patients

almost 15 years ago

ASH 2010: Brentuximab Vedotin Produces High Response Rate in Relapsed or Refractory Hodgkin Lymphoma

almost 15 years ago

ASH 2010: Bosutinib Shows Promise as First-line Treatment of Chronic Myelogenous Leukemia

almost 15 years ago

ASH 2010: Multiple Benefits Observed for Bortezomib in Newly Diagnosed Myeloma Patients

almost 15 years ago

FDA Green-Lights Phase III Trial for Drug-Eluting Microspheres in Liver Cancer

almost 15 years ago

FDA Requests Label Change for Generic Docetaxel

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