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| | | ![]() FDA Grants Fast Track Designation for the Investigation of Zactima (ZD6474) for Treatment of Thyroid Cancer WILMINGTON, DE -- February 2, 2006 -- AstraZeneca announced today during their Fourth Quarter and Full Year Results meeting that the US Food and Drug Administration (FDA) has granted fast track designation for the investigation of Zactima(TM) (ZD6474) in treating medullary thyroid carcinoma. For advanced thyroid cancer, there is currently no curative modality or approved chemotherapy. Zactima also received orphan-drug designation last year for the treatment of patients with follicular, medullary, anaplastic, and locally advanced and metastatic papillary thyroid cancer. "We are pleased to receive fast track designation for Zactima for the treatment of medullary thyroid cancer, and are committed to evaluating the potential of Zactima as a new treatment option for patients with this disease," said Peter Langmuir, MD, Senior Director, Medical Science, AstraZeneca. The fast track designation provides AstraZeneca certain benefits that may facilitate the drug development and regulatory submission processes, including the opportunity to seek FDA input into development plans, the option of a rolling submission of the New Drug Application (NDA), and the option of requesting evaluation of studies using surrogate endpoints. This designation is intended to facilitate the development and expedite the review of investigational drugs that are intended to treat serious or life-threatening conditions and that demonstrate the potential to address unmet medical needs. Zactima is being evaluated in a phase 2 clinical trial in medullary thyroid cancer, and AstraZeneca is currently enrolling patients in a single arm phase 2 Zactima study in locally advanced or metastatic hereditary medullary thyroid cancer. Phase 3 clinical trials in another tumor type, advanced non-small-cell lung cancer, are scheduled to start in the near future. About Zactima About Thyroid Cancer
SOURCE: AstraZeneca
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