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The FDA last week granted
regular approval to Novartis Pharmaceuticals Corp.’s Tabrecta
for the treatment of metastatic non-small cell lung cancer (NSCLC) in adults
whose tumors have the mesenchymal-epithelial transition (MET) gene, a rare
mutation found in about 4% of patients. The kinase inhibitor received
accelerated approval in May 2020, based on positive clinical trial data. For
the treatment of NSCLC, Tabrecta currently holds covered or better status for
93% of all insured lives under the pharmacy benefit. About 25% of insured
lives have preferred access to Tabrecta. |
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Source: MMIT Analytics,
as of 8/17/22 |
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