Friday, April 24, 2015

FDA grants U.K.'s Tremelimumab orphan drug status for Mesothelioma

The U.K.-based pharmaceutical company AstraZeneca announced that the U.S. Food & Drug Administration (FDA) has granted Tremelimumab orphan drug status for the treatment of malignant mesothelioma.
Robert Iannone, Head of Immuno-oncology at AstraZeneca's Global Medicines Development division, said that there is a crucial need to develop additional Mesothelioma treatments, since less than 5% of the deadly Cancer's victims live more than five years. “Our aim is to rapidly advance the development of Tremelimumab,” Iannone stated, adding that the company hoped the drug would become a viable new option for treatment of the disease.
Tremelimumab is an anti-CTLA-4 monoclonal antibody, which means that it blocks production of an inhibitor that destroys Cytotoxic T lymphocytes (CTLs), a type of white blood cell produced naturally by the body that can recognize and kill cancer. With the inhibitor blocked, the body can produce potentially Cancer-defeating CTLA-4 antibodies more quickly.


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