Novartis AG has become the latest company to win US Food and Drug Administration approval for a tumor-agnostic cancer indication, in this case for the BRAF inhibitor Tafinlar (dabrafenib) and the MEK inhibitor Mekinist (trametinib), for solid tumors carrying BRAF V600E mutations. The two-drug combination is the first to win approval in that indication but joins a list of drugs that have secured biomarker-driven, tissue-agnostic labels since 2017, which reflects the growing view of cancers as genomic diseases.
Novartis said 22 June that the FDA granted accelerated approval to Tafinlar/Mekinist in children and adults aged 6 and older...








