Teikoku Pharma USA, Inc. announces FDA approval of docetaxel injection

First non-alcohol formulation approved in the US.

The main difference, compared to other docetaxel formulations, is that docetaxel injection is the first non-alcohol formulation approved in the US. Further differentiating it from some of the currently marketed docetaxel formulations is that Teikoku's docetaxel injection:

The need for non-alcohol docetaxel gained visibility in June 2014 when FDA issued a Drug Safety Communication warning patients that docetaxel may cause symptoms of alcohol intoxication after treatment. Manufacturers of docetaxel formulations for domestic use were subsequently required to revise their product labels to warn about this risk. Some US hospitals and clinics require patients to wait two or more hours after treatment with docetaxel before they can be released. The company's formulation of docetaxel was specifically developed to address these concerns.

"Docetaxel injection addresses a compelling need in the docetaxel market. As the first alcohol-free formulation approved in the US, we believe the benefits of this novel formulation will provide an option for patients with alcohol sensitivity or a preference for an alcohol-free treatment. We are excited to add alcohol-free docetaxel to our growing portfolio of differentiated injectable products and believe it has the potential to improve the lives of patients, resolve concerns among health care professionals at hospitals and infusion centers, and ultimately drive value for Eagle stakeholders," said Scott Tarriff, President and CEO of Eagle Pharmaceuticals.

"The approval of docetaxel injection, our first oncology product, is a significant milestone in Teikoku's history, and docetaxel injection marks our second FDA-approved product as New Drug Application (NDA). In addition, Eagle Pharmaceuticals' strong presence in the oncology space makes Eagle an excellent partner for our product," said Paul Mori, President and CEO of Teikoku.