Genentech: FDA Approves New Indication for Tecentriq in Certain Lung Cancers
May 18 2020 - 4:32PM
Dow Jones News
By Stephen Nakrosis
Genentech on Monday said the U.S. Food and Drug Administration
approved its Tecentriq to treat certain patients with metastatic
non-small cell lung cancer.
The company said the approval of Tecentriq, or atezolizumab, was
based on an interim analysis of its Phase III IMpower110 study
"showing Tecentriq demonstrated a significant overall survival
benefit in people with high PD-L1 expression compared with
chemotherapy."
Genentech also said the latest approval was "Tecentriq's fourth
indication in metastatic non-small cell lung cancer and fifth
indication in lung cancer overall."
Tecentriq is the only single-agent cancer immunotherapy with
three dosing options, Genentech said.
The company "has an extensive development program for Tecentriq,
including multiple ongoing and planned Phase III studies across
lung, genitourinary, skin, breast, gastrointestinal, gynecological
and head and neck cancers. This includes studies evaluating
Tecentriq both alone and in combination with other medicines," it
said.
Genentech is a member of the Roche Group.
--Write to Stephen Nakrosis at stephen.nakrosis@wsj.com
(END) Dow Jones Newswires
May 18, 2020 16:17 ET (20:17 GMT)
Copyright (c) 2020 Dow Jones & Company, Inc.
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