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Hospira's topotecan injection receives US FDA approval to treat SCLC
Lake Forest, Illinois | Saturday, February 5, 2011, 13:00 Hrs  [IST]

Hospira, Inc. the world leader in generic injectable pharmaceuticals, announced US Food and Drug Administration (FDA) approval of Topotecan Injection, the first solution formulation of the oncology drug approved in the United States. The medication is a generic version of Hycamtin, which had 2010 US sales of more than $140 million. Hospira's topotecan is indicated for treatment of Small Cell Lung Cancer (SCLC) sensitive disease after failure of first-line chemotherapy.

The solution formulation of topotecan, with a concentration of 4 mg/4 ml, is designed to improve caregiver convenience and safety, and Hospira expects to launch the product by the end of February.

“Hospira's solution version of topotecan expands our portfolio of value-added generics,” said Thomas Moore, president, US, Hospira. “We're excited to offer the medical community access to a lower-cost, more convenient version of this key oncolytic.”

Hospira's Specialty Injectable Pharmaceuticals (SIP) offering includes approximately 200 generic injectable drugs in many dosages and formulations. In addition, many of its products are available in popular differentiated presentations, several of which are proprietary, such as ADD-Vantage drug delivery system and iSecure pre-filled syringes. Therapeutic segments include analgesia, anaesthesia, anti-infectives, cardiovascular, oncology, emergency and other areas. Hospira also has robust pipelines of both generic and bio-similar drugs.

Hospira, Inc. is a global specialty pharmaceutical and medication delivery company dedicated to Advancing Wellness. The company offers one of the broadest portfolios of generic acute-care and oncology injectables, as well as integrated infusion therapy and medication management solutions.

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