Pfizer, Biogen among hundreds of US drugmakers calling for abortion pill
ruling reversal
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[April 11, 2023]
By Michael Erman and Ahmed Aboulenein
(Reuters) -Executives from more than 300 biotech and pharmaceutical
industry companies, including Pfizer Inc and Biogen Inc, signed an open
letter on Monday calling for reversal of a federal judge's decision to
suspend sales of the abortion pill mifepristone.
A U.S. judge on Friday suspended the U.S. Food and Drug Administration's
2000 approval of the drug, effectively banning sales while a case
brought by anti-abortion groups before him continues in the Northern
District of Texas.
Last week's ruling by Judge Matthew Kacsmaryk undermines the FDA's
authority, the letter's authors wrote, adding that it ignores decades of
scientific evidence and legal precedent.
"We call for the reversal of this decision to disregard science, and the
appropriate restitution of the mandate for the safety and efficacy of
medicines for all with the FDA, the agency entrusted to do so in the
first place," they wrote.
Pfizer Chief Executive Albert Bourla was the first leader of a major
pharmaceutical company to add his name to the letter, which also bore
the signatures of more than 300 executives from smaller U.S.
biotechnology companies. Biogen President Alisha Alaimo has since also
signed it.
The White House welcomed the move, issuing a statement drawing attention
to and quoting from the letter.
The Department of Justice appealed the decision in a filing with the 5th
U.S. Circuit Court of Appeals on Monday. It asked that the decision be
stayed by April 13, and that a stay remain in place until all appeals,
including if necessary to the Supreme Court, are resolved.
The letter was written by ReCode Therapeutics CEO Shehnaaz Suliman,
Blackfynn co-founder Amanda Banks, and Ovid Therapeutics CEO Jeremy
Levin, who is also a former chairman of biotech industry lobbying group
BIO.
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Signage is seen outside of the Food and
Drug Administration (FDA) headquarters in White Oak, Maryland, U.S.,
August 29, 2020. REUTERS/Andrew Kelly
The decision puts the entire
industry at risk, the letter says, and sets a precedent for
undermining the agency's authority to approve drugs, adding
regulatory uncertainty that they warned would disincentivize
investment in new treatments.
"You have the real potential of having medicines not being developed
because it's far too expensive, or medicines that are currently
approved being withdrawn because they are political," Levin told
Reuters.
The FDA approved mifepristone, part of a two-drug regimen that
accounts for more than half of U.S. abortions, more than 20 years
ago and has determined its safety several times since.
Health policy and legal experts have said that if Kacsmaryk's
unprecedented ruling is allowed to stand it could undermine
confidence in FDA's authority to regulate drugs, severely weaken the
agency, and hinder access to new treatments.
"If courts can overturn drug approvals without regard for science or
evidence, or for the complexity required to fully vet the safety and
efficacy of new drugs, any medicine is at risk for the same outcome
as mifepristone," the letter said.
The ruling could open the possibility of the banning of vaccines and
contraception for women, said Levin.
"This is a nightmare scenario for the industry," he said. "It's the
single worst threat to the industry in over 50 years."
(Reporting by Michael Erman in New York and Ahmed Aboulenein in
Washington; Additional reporting by Bhanvi Satija in Bengaluru;
Editing by Bill Berkrot)
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