Eli Lilly Alzheimer's drug setback extends rival Biogen's lead
Send a link to a friend
[January 21, 2023]
(Reuters) -The U.S. health regulator's rejection of accelerated
approval for Eli Lilly and Co's Alzheimer's disease drug extends the
market lead for rivals Eisai and Biogen's treatment by months, analysts
said.
The U.S. Food and Drug Administration (FDA) declined to approve
donanemab's application because Lilly had not submitted data from enough
patients who were treated for at least a year, the drugmaker said late
Thursday.
"This is a modest positive for Biogen" because it delays donanemab's
launch, Jefferies analyst Michael Yee said, adding that Eli Lilly could
file for traditional approval by mid-2023.
Lilly's shares fell 1.3% to $346.6, while Biogen Inc's shares rose 1.5%
to $284.5 in morning trade on Friday.
"Lilly's inability to launch donanemab near-term will prevent them from
expediting their launch post-full approval by depriving them of the
ability to begin to educate physicians and patients," said Citi analyst
Andrew Baum.
The setback for Lilly comes just weeks after the FDA granted Japanese
drugmaker Eisai Co Ltd and partner Biogen accelerated approval for their
Alzheimer's drug Leqembi.
[to top of second column]
|
A sign marks a Biogen facility in
Cambridge, Massachusetts, U.S. January 26, 2017. REUTERS/Brian
Snyder/File Photo
Analysts are waiting for the
traditional approval of Biogen's drug, expected in the next few
months, and for wider health insurance coverage before they expect
sales of the drug to pick up.
The U.S. government's Medicare health plan currently reimburses
Alzheimer's disease drugs with accelerated approval only if patients
are enrolled in a validated clinical study.
Lilly expects to report data from a late-stage trial of donanemab in
the second quarter, which would form the basis of the drug's
application seeking traditional FDA approval shortly thereafter.
"But if there is anything wrong with the (Eli Lilly) data set, it is
easier to reject an unapproved drug than remove an approved drug
from market," said Baird analyst Brian Skorney.
(Reporting by Khushi Mandowara in Bengaluru; Editing by Shailesh
Kuber)
[© 2023 Thomson Reuters. All rights
reserved.]
This material may not be published,
broadcast, rewritten or redistributed.
Thompson Reuters is solely responsible for this content. |