AbbVie’s Solid Tumor Strategy Gets a Win With Accelerated FDA Approval in Lung Cancer
8 Articles
8 Articles
AbbVie’s Solid Tumor Strategy Gets a Win With Accelerated FDA Approval in Lung Cancer
Emrelis, an antibody drug conjugate developed by AbbVie, is now FDA approved for patients whose non-small cell lung cancer overexpresses the protein c-Met. The pharma company said this ADC is its first internally developed solid tumor medicine as well as its first solid tumor FDA approval in lung cancer. The post AbbVie’s Solid Tumor Strategy Gets a Win With Accelerated FDA Approval in Lung Cancer appeared first on MedCity News.
US FDA approves AbbVie’s drug for a type of lung cancer
(Reuters) -The U.S. Food and Drug Administration has approved AbbVie’s drug to treat adults with a type of lung cancer who have received previous treatment, the drugmaker said on Wednesday. The treatment, branded as Emrelis, belongs to a class of drugs known as antibody-drug conjugates (ADC) which are targeted cancer therapies. Emrelis was approved for previously treated patients with non-squamous non-small cell lung cancer whose disease has spr…
FDA gives AbbVie accelerated approval for antibody-drug conjugate in lung cancer
The FDA approved a new antibody-drug conjugate from AbbVie on Wednesday to treat patients with certain kinds of lung cancer. Regulators granted accelerated approval to telisotuzumab vedotin in second-line non-small cell lung cancer for patients ...
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