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Home » Latest News » US Court » Court To Weigh Bid To Ban Abortion Pill In US

Court To Weigh Bid To Ban Abortion Pill In US

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October 19, 2026
Court To Weigh Bid To Ban Abortion Pill In US
Court To Weigh Bid To Ban Abortion Pill In US

 

A Texas courtroom will be the latest battleground for US abortion rights hoping for a national ban on a widely used abortion pill when their lawsuit against government drug regulators is argued.

Anti-abortion forces are targeting the prescription drug mifepristone in their campaign to win a total ban on the practice after the US Supreme Court ended the nationwide right to abortion last June, a

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The suit against the US Food and Drug Administration (FDA) aims at a pill involved in 53 percent of all abortions in the United States, or more than a half-million every year.
While the FDA has never been challenged like this before on its approval of a drug that has proven safe and effective, the plaintiffs, a coalition of anti-abortion groups, believe they can win a national freeze on distribution of mifepristone.
Presiding over the case in federal court in Amarillo, Texas will be Judge Matthew Kacsmaryk, a deeply conservative Christian with a personal history of opposition to abortion and a court record of favoring right-wing causes.

One component of a two-drug regimen used for medication abortion, mifepristone has been used by an estimated 5.6 million women to terminate pregnancies since its approval, according to the FDA.

It has a long safety record, and the FDA estimates 5.6 million Americans have used it to terminate pregnancies since it was approved.

 

But the Alliance Defending Freedom, a Christian advocacy group, sued the FDA saying the approval of mifepristone “disavow(ed)” science, “ignored” potential health impacts and “disregarded” the complications that can arise with its use.

 

“The FDA failed America’s women and girls when it chose politics over science and approved chemical abortion drugs for use in the United States,” they said.

 

The FDA has urged the judge to reject the request.

 

“The public interest would be dramatically harmed by effectively withdrawing from the marketplace a safe and effective drug that has lawfully been on the market for 22 years,” it said.

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