Zevalin expansion gets FDA approval, continued ...
“We believe the approval of Zevalin as an effective treatment option following a first-line regimen represents a notable advance in the treatment of non-Hodgkin’s Lymphoma,” says Rajesh C. Shrotriya, M.D., chairman, CEO and president of the company.
The updated indication was based on data collected during the First-line Indolent Therapy Study, which evaluated the safety and efficacy of the treatment in more than 400 patients with follicular Non-Hodgkin's lymphoma who had achieved a partial or complete response following a chemotherapy regimen. The three and one-half year follow-up found that when the drug is used as part of first-line chemotherapy for these patients, Zevalin improved the progression-free survival time from 18 months to 38 months.
Spectrum Pharmaceuticals is a commercial-stage biotechnology company that focuses in oncology. << PREVIOUS PAGE