Moderna flu shot succeeds in late-stage study
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[September 14, 2023]
By Patrick Wingrove
(Reuters) -Moderna on Wednesday said its flu vaccine had generated a
stronger immune response against all four A and B strains of the
influenza virus compared to traditional flu shots in a late-stage trial.
Shares of the U.S. biotech closed more than 3% higher at $108.59 on
Wednesday.
The effectiveness of Moderna's flu vaccine was demonstrated across all
age groups, including older people, and was found to be safe and
tolerable, according to the company. Moderna also said it had found that
its shot was equal or superior to Sanofi's high-dose flu vaccine in a
separate early head-to-head study.
Moderna could use this data to file for accelerated approval of its flu
shot in the United States by year-end, and likely launch the vaccine by
the 2024/2025 season, Jefferies analyst Michael Yee said in a note.
The company had previously said that there was not enough available data
to determine whether the flu vaccine would succeed after it failed to
meet the "early-success" criteria in the study.
Moderna also announced that it was scaling down manufacturing of its
COVID-19 vaccine, an updated version of which was approved this week by
U.S. regulators, to align with lower post-pandemic demand and help the
company sooner hit its target of 75%-80% gross margin growth.
"We probably overproduced a little bit too much this year, which is why
we have excessive unutilized capacity and excessive materials, and that
will come down," Moderna CFO Jamey Mock said during the investor day
conference.
Moderna said it could launch up to 15 products over the next five years,
as it moves focus away from its COVID vaccine.
SCALING DOWN ON COVID SHOTS
The company is in talks with its partners that fill vials and syringes
with its messenger RNA-based COVID vaccines globally to downsize
production, Stephen Hoge, president of the Massachusetts-based company,
said in an interview.
The downsizing, Hoge added, will help Moderna adjust to the endemic
phase of the disease, which had led to falling demand for COVID vaccines
as payers scale back orders for the shots.
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A vial and a syringe are seen in front of a displayed Moderna logo,
in this illustration taken, November 27, 2021. REUTERS/Dado Ruvic/Illustration/File
Photo
Moderna in August predicted that
U.S. demand for the vaccine would reach 50 million to 100 million
doses in the fall season. About 153.8 million COVID shots were
administered in the United States in 2022, according to the U.S.
Centers for Disease Control and Prevention.
"Over the past couple of years, we've been in pandemic mode
producing a billion doses a year," Hoge said. "We've been waiting
for the moment when the pandemic was officially behind us that we
would need to restructure that manufacturing footprint."
Following the U.S. Food and Drug Administration's authorization on
Monday, Moderna said it would start shipping COVID vaccine doses
across the United States.
The company has deals to supply other countries with its COVID shot
including Britain, Canada and Japan, but does not yet have an
agreement with the EU, according to Hoge, who also said COVID was
the focus of Moderna's manufacturing agreement with China.
Hoge said that while Moderna was urgently working on downsizing
COVID manufacturing, talks with third-party manufacturers - which
will help produce the upcoming respiratory syncytial virus (RSV) and
influenza vaccines that investors hope will start to replace
Moderna's waning COVID revenue - could spill into next year.
"These are relationships that we will need for decades to come,"
Hoge said.
Moderna declined to identify the partners but has previously said
they include Thermo Fisher, Sanofi, Catalent.
Spain's Rovi, which has a 10-year deal with Moderna to manufacture
mRNA-based therapies, said that it does not expect to cut down its
vaccine production, at least this year.
"The vaccine's manufacturing runs from June to October and we are
already producing it. All the purchase orders are being fulfilled,"
a Rovi spokesperson said, referring to the COVID vaccine.
(Reporting by Patrick Wingrove in New York; Bhanvi Satija and Mariam
Sunny in Bengaluru; Editing by Will Dunham, Mark Porter and Daniel
Wallis)
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