Exclusive-Tens of millions of J&J COVID-19 shots sit at Baltimore
factory -sources
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[October 28, 2021]
By Carl O'Donnell
(Reuters) - An estimated 30 million to 50
million doses of Johnson & Johnson's COVID-19 vaccine made early this
year sits idle in Emergent BioSolutions Inc's plant in Baltimore
awaiting a green light from U.S. regulators to ship, two sources
familiar with the matter said.
Emergent, a contract drug manufacturer, is waiting for the U.S. Food and
Drug Administration to approve release of those doses. The agency must
still inspect and authorize the plant before Emergent can ship newly
manufactured drug substance, one of the sources said.
The exact number of doses sitting idle cannot be determined, the source
said, because Emergent only makes raw vaccine substance and does not
fill vials with finished product.
The FDA in April halted operations at Emergent's production facility
after J&J's vaccine was found to be contaminated with material from
AstraZeneca's COVID-19 shots, which were also being manufactured there
at the time.
The contamination ruined about 15 million J&J doses and set back its
U.S. vaccine rollout by weeks.
Material manufactured for the J&J vaccine at the Baltimore plant prior
to the April shutdown and awaiting FDA approval could be enough to
produce as many as 50 million shots, the two sources said. They asked
not to be named because they were not authorized to speak publicly on
the issue.
Of the 100 million doses worth of vaccine material Emergent described in
an April Congressional hearing as being sidelined, the FDA has so far
cleared nine batches of J&J's vaccine and three batches of
AstraZeneca's. It has not disclosed how many doses were in those
batches.
Emergent in late July said it would resume production of J&J's vaccine
at the plant following additional FDA reviews, but has not provided
updates on production or timing of potential shipments. [L1N2P535Q]
Emergent has begun making new vaccine substance, but the FDA has yet to
provide guidance on when it plans to inspect the Baltimore facility, one
of the sources said.
The FDA said in a statement that it conducted a limited inspection of
Emergent's facility in July to confirm it had conducted corrective
actions following the April production pause. A previous inspection had
turned up a raft of sanitary, safety and bad manufacturing practice
issues at the plant.
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A box of Johnson & Johnson's coronavirus disease (COVID-19) vaccines
is seen at the Forem vaccination centre in Pamplona, Spain, April
22, 2021. REUTERS/Vincent West/File Photo
The agency said it has not yet authorized the
facility to ship doses and continues to review batches made prior to
the production halt. It has based its batch approvals on reviews of
facility records and quality testing conducted by the manufacturer.
The FDA typically waits for a drug manufacturing facility to produce
multiple batches of its product before conducting an inspection,
according to a former FDA official who asked not to be named because
she was not authorized to speak with the media.
Following the Emergent plant shutdown, J&J lowered its production
target for 2021 to between 500 million and 600 million doses from
around 1 billion. It expects to be able to make 1 billion doses
annually starting next year.
J&J has not specified whether it needs Emergent to restart
production to hit its 2022 target. It has another manufacturing
facility in Leiden, Netherlands, and production agreements with
other contract manufacturers, including Catalent Inc and India's
Biological E.
The United States contracted with J&J for 100 million shots in 2020
and ordered an additional 100 million in March.
Last week, the FDA authorized J&J's vaccine as a booster for people
who are already vaccinated but desire additional protection against
COVID-19, including anyone over age 18 who originally received the
company's single-dose shot.
Use of J&J's vaccine fell sharply in the United States after it was
linked to a rare but potentially lethal blood clotting disorder.
(Reporting by Carl O'Donnell; Editing by Caroline Humer and Bill
Berkrot)
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