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FDA Approves xT CDx, a NGS-Based in Vitro Diagnostic Device

The FDA has approved xT CDx, a 648-gene next-generation sequencing assay for solid tumor profiling, and companion diagnostic for patients with colorectal cancer.

FDA Expands Lilly s Erbitux Label With Braftovi For Treatment Of Metastatic Colorectal Cancer

INDIANAPOLIS (dpa-AFX) - Eli Lilly and Co. (LLY) said that the U.S. Food and Drug Administration has granted approval of a new indication for Erbitux or cetuximab injection in combination with

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