Last year, a Texas federal judge’s decision to revoke the Food and Drug Administration’s (FDA) approval of the abortion pill mifepristone ignited a nationwide controversy over abortion rights. The legal skirmish over the pill has escalated further following the retraction of a key scientific paper that played a pivotal role in the case.
In 2021, Sage Journals published a study suggesting that mifepristone significantly increases the risk of women requiring emergency room care after an abortion. This study was cited by Texas District Judge Matthew Kacsmaryk in his April ruling against the FDA’s approval of the pill. Recently, Sage announced the retraction of this study and two others by lead author James Studnicki, criticizing the research for its lack of scientific rigor and accusing the author of undeclared conflicts of interest.
Sage commissioned two independent experts for a post-publication review of the papers. The experts identified “fundamental problems,” undermining the authors’ conclusions. Studnicki, in a rebuttal shared with Wired, denounced the retractions as “unjustified” and described Sage’s action as a “baseless ideological attack.”
Sage highlighted that Studnicki and his co-authors had declared no conflicts of interest upon submitting their research. However, Studnicki serves as vice president of the Charlotte Lozier Institute, the research arm of Susan B. Anthony Pro-Life America, a prominent anti-abortion organization.
Studnicki maintains that his affiliation with anti-abortion groups was “fully known and identified to Sage” at the time of submission.
The future of the Texas ruling now rests with the Supreme Court, following a federal appeals court’s decision that mifepristone should stay accessible to patients while the lawsuit against the FDA proceeds.
The Supreme Court is scheduled to hear arguments on the matter in March, marking the first abortion case since the landmark 2021 Dobbs decision, which overturned Roe v. Wade and ended federal protection for abortion rights.