Genta, a US biopharmaceutical company focused on delivering innovative products for the treatment of cancer, has initiated a new clinical trial with its novel, orally-absorbed, semi-synthetic taxane oncology drug tesetaxel, after the US Food and Drug Administration gave the trials the go-ahead (Marketletter June 30, 2008).
Unlike standard taxanes such as paclitaxel, which must be infused intravenously, tesetaxel is administered as a capsule. The new study will examine the clinical pharmacology of the drug over a narrow dosing range around that established in Phase II studies.
"Taxanes are the most widely used class of anticancer compounds," said chief medical officer Loretta Itri. "Successful development of an oral taxane has been a research goal that has eluded many pharmaceutical companies. Tesetaxel has already been tested in more than 250 patients with various types of cancer in the USA, Europe and Japan. By eliminating serious hypersensitivity infusion reactions, as well as potentially reducing nerve damage and overcoming resistance to standard taxanes, tesetaxel may offer important new treatment options for patients with advanced cancer," she added.
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