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Alemtuzumab is currently not available.
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Information about CancerDrugsDirect.com
List of countries where we can ship Alemtuzumab:
Latest news releases on Alemtuzumab:
May 7, 2012 (New Orleans, Louisiana) — Full results of a second phase 3 trial of alemtuzumab (Lemtrada, Genzyme/Sanofi) in patients with relapsing-remitting multiple sclerosis (MS) who had relapsed while receiving previous treatment show that the still ...
Genzyme presented additional data at the 64th Annual Meeting of the American Academy of Neurology from its Phase II CARE-MS II trial, which demonstrated that the Expanded Disability Status Scale (EDSS), i.e. a standard assessment of physical ...
Accumulation of disability was significantly slowed in patients with multiple sclerosis (MS) who were treated with alemtuzumab versus Rebif (high dose subcutaneous interferon beta-1a), as measured by the Expanded Disability Status Scale (EDSS), a standard ...
Genzyme, a Sanofi company (NYSE: SNY), announced that 12 data presentations, including six platform presentations, from the company’s multiple sclerosis (MS) clinical trial programs for alemtuzumab and teriflunomide will be featured at the American ...
There is no molecule in Phase III of development. The only molecule in Phase II/III is alemtuzumab. Alemtuzumab is under investigation as a conditioning regimen for patients with severe aplastic anemia who are undergoing allogeneic stem cell ...
One of the drugs on the horizon is a yearly IV infusion called Alemtuzumab. This drug was studied in over 800 patients with relapsing MS, and results show that it is more effective in treating this type of MS than standard 3-times per week injections of ...
Founded in 1999, the company's first marketed antibody, ofatumumab (Arzerra(r)), was approved to treat chronic lymphocytic leukemia in patients who are refractory to fludarabine and alemtuzumab after less than eight years in development.
Founded in 1999, the company's first marketed antibody, ofatumumab (Arzerra(r)), was approved to treat chronic lymphocytic leukemia in patients who are refractory to fludarabine and alemtuzumab after less than eight years in development. Genmab's validated ...
Founded in 1999, the company's first marketed antibody, ofatumumab (Arzerra(r)), was approved to treat chronic lymphocytic leukemia in patients who are refractory to fludarabine and alemtuzumab after less than eight years in development. Genmab's validated ...