Glaxo breast cancer pill wins FDA approval

By Susan Heavey

WASHINGTON (Reuters) - GlaxoSmithKline Plc won U.S. approval for a once-a-day breast cancer pill on Tuesday that the drugmaker hopes will launch a new era for its oncology business.

The Food and Drug Administration cleared the drug, called Tykerb, for patients with advanced breast cancer in combination with Roche Holding AG's oral chemotherapy drug, Xeloda, or capecitabine.

It is the first of four cancer drugs that Glaxo hopes to have approved by 2010. Studies of Tykerb, or lapatinib, to treat early-stage and inflammatory breast cancers, as well as head/neck, gastric and lung cancers, are also underway.

For now, the FDA approved Tykerb for patients with HER-2 positive breast cancer who no longer respond to Roche and Genentech Inc.'s rival product, Herceptin.

Patients should have also tried anthracycline and taxane chemotherapy drugs such as Sanofi-Aventis's, Taxotere, or Bristol-Myers Squibb's, Taxol.

"New targeted therapies such as Tykerb are helping expand options for patients," said Dr. Steven Galson, head of the FDA's Center for Drug Evaluation and Research.

Side effects can include diarrhea, nausea and rash, as well as numbness and other discomfort in the hands and feet.

Overall, nearly 182,000 women were diagnosed with breast cancer and another nearly 42,000 died from it in 2003, based on the most recent data available from the U.S. Centers for Disease Control and Prevention. Men are also at risk.