Novartis Receives FDA Accelerated Approval for Lung-Cancer Treatment, Diagnostic
07 May 2020 - 4:02PM
Dow Jones News
By Matteo Castia
Novartis AG said Thursday that the Food and Drug Administration
has approved its lung cancer treatment Tabrecta and the associated
diagnostic FoundationOne.
"This indication is approved under accelerated approval based on
overall response rate and duration of response. Continued approval
for this indication may be contingent upon verification and
description of clinical benefit in confirmatory trials," the pharma
giant said.
Tabrecta is a MET kinase inhibitor for adult patients with
metastatic nonsmall cell lung cancer whose tumors have a mutation
that leads to MET exon 14 skipping.
FoundationOne is a diagnostic that helps detecting mutations
leading to MET exon 14 skipping in tumor tissue.
Write to Matteo Castia at matteo.castia@dowjones.com
(END) Dow Jones Newswires
May 07, 2020 01:47 ET (05:47 GMT)
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