U.S. FDA accepts Biogen's ALS therapy for review
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[July 27, 2022]
(Reuters) -Biogen Inc's treatment
for a rare type of amyotrophic lateral sclerosis (ALS) was accepted for
review by the U.S. health regulator, weeks after follow-up analyses of
data from a failed late-stage study suggested the drug was likely to
work.
The company said the U.S. Food and Drug Administration's decision on its
treatment, tofersen, which will go through a priority review, is
expected by Jan. 25, 2023. The FDA also plans to hold a meeting of its
outside experts to discuss the application.
Biogen is seeking approval of tofersen for ALS patients with mutations
in a specific gene that leads to accumulation of toxic levels of a
protein called SOD1. If approved, it will be the first treatment to
target a genetic cause of ALS.
Tofersen in October failed to meet the main goal of a late-stage study
and did not show statistically significant improvement in the functional
status of patients with fast-progressing ALS.
Later in June, the company said analyses of data from the study
suggested that early administration was effective in slowing progression
of ALS in patients with SOD1 mutation.
Biogen also said it was seeking approval for tofersen based on changes
produced in a protein called neurofilament during the study which the
company says is "reasonably likely to predict clinical benefit."
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Biogen logo is seen displayed in this illustration taken, May 3,
2022. REUTERS/Dado Ruvic/Illustration
"We do think that tofersen -
symbolically - represents a highly important benchmark for FDA
flexibility in neurodegeneration," said Stifel analyst Paul Matteis.
Biogen is seeking approval under the FDA's accelerated approval
pathway.
The pathway, mainly for rare diseases that have had no effective
treatments, has come under increasing scrutiny after the FDA used it
last year to approve Biogen's controversial Alzheimer's Disease drug
despite efficacy concerns.
Biogen licensed tofersen from Ionis Pharmaceuticals Inc in 2018.
(Reporting by Mrinalika Roy in Bengaluru; Editing by Shinjini
Ganguli)
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