FDA officials want to withdraw the drug because of a lack of evidence of its efficacy and because of side effects
TUESDAY, Oct. 18, 2022 (HealthDay News) — In a three-day hearing that began Monday, a U.S. Food and Drug Administration advisory committee will give the maker of a drug meant to prevent premature births a chance to show why its drug should not be pulled off the market.
FDA officials have said they want to withdraw the medication Makena because of a lack of evidence that it works and due to its side effects. The drug was initially allowed as part of the agency’s accelerated approval program, which lets a medication launch after promising early results while larger studies test it further.
“Based on the evidence shown today, Makena is not shown to be effective,” Patrizia Cavazzoni, director of the FDA Center for Drug Evaluation and Research, said in opening remarks on Monday, the Associated Press reported. “Its benefit-and-risk profile is unfavorable, and it should be withdrawn from the market.”
Complicating the issue is that Makena, a weekly injectable, is the only medication that exists to help prevent preterm birth, the AP reported.
“The need for an effective treatment for preterm birth is great,” the American College of Obstetricians and Gynecologists said. “Makena and its associated generics represent the only treatment currently available to obstetrician-gynecologists to help prevent this condition.”
At the hearing, FDA staff and company scientists will each present their arguments. The FDA panel of outside experts will vote on the issue at the conclusion of the hearing on Wednesday, but the agency will still make the final decision about whether to order a withdrawal, the AP reported.
Makena has been on the marketplace since 2011, when a small study showed it reduced rates of early delivery in women with a history of early delivery, the AP reported. But a 2019 international study of 1,700 women revealed the drug did not reduce premature births but could cause side effects, including blood clots and depression. The drugmaker, Covis, has said the later study was flawed. Only 7 percent of participants were Black women, who have a higher risk for preterm birth, compared with 59 percent who participated in the original U.S. study, the company said. Covis wants to conduct another study with higher-risk patients, especially Black Americans.
Associated Press Article
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