Bayer Phase 3 Lymphoma Study Meets Primary Endpoint
October 14 2020 - 3:34AM
Dow Jones News
By Cecilia Butini
Bayer AG said Wednesday that its CHRONOS-3 Phase 3 study for a
combination of two drugs to treat relapsed indolent non-Hodgkin's
Lymphoma has met its primary endpoint of significantly prolonging
patients' progression-free survival.
Progression-free survival is understood as the amount of time
after treatment that a patient can live with a disease without it
worsening.
The German chemicals and pharmaceuticals major said the study
examined a combination of copanlisib and rituximab, and that no new
safety signals were identified in the combination. Safety and
tolerability of the two drugs combined were consistent with
previously available data on the drugs taken individually, the
company said.
Copanlisib is already approved in the U.S. under the accelerated
approval pathway for the treatment of adult patients with relapsed
follicular lymphoma, Bayer said.
Write to Cecilia Butini at cecilia.butini@wsj.com
(END) Dow Jones Newswires
October 14, 2020 03:19 ET (07:19 GMT)
Copyright (c) 2020 Dow Jones & Company, Inc.
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