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Newly approved medication for postpartum depression has ties to Triangle researchers

Samantha Meltzer-Brody, the founder and director of the UNC Medical Center’s Perinatal Psychiatry Program which is home to the first inpatient treatment unit for women with postpartum depression in the U.S., stands for a portrait before meeting with her team on Wednesday, Apr. 24, 2019, in Chapel Hill, NC. Recently, her research was instrumental in the FDA’s approval of the first drug to treat the disorder.
Samantha Meltzer-Brody, the founder and director of the UNC Medical Center’s Perinatal Psychiatry Program which is home to the first inpatient treatment unit for women with postpartum depression in the U.S., stands for a portrait before meeting with her team on Wednesday, Apr. 24, 2019, in Chapel Hill, NC. Recently, her research was instrumental in the FDA’s approval of the first drug to treat the disorder. ctoth@newsobserver.com

On Friday, the Food and Drug Administration approved the first oral medication for postpartum depression.

The approval of this medication is, in part, thanks to research from the Triangle.

Here’s what to know:

What is Zurzuvae?

Zurzuvae is the first pill targeted at depression that occurs shortly after childbirth.

Unlike other antidepressants, which typically take weeks to start working, this pill can start to reduce symptoms in as few as three days. Patients take the pill once a day for two weeks.

“Having access to an oral medication will be a beneficial option for many of these women coping with extreme, and sometimes life-threatening, feelings,” Dr. Tiffany Farchione, the FDA’s director of psychiatric drugs, said in a press release.

Postpartum depression is a leading cause of maternal mortality and can prevent infants from properly bonding with their mothers. A CDC study found that one in eight U.S. women who recently gave birth had symptoms of PPD.

Risk factors for PPD include:

  • Family history of depression
  • Low social support
  • Pregnancy and birth complications

Who is Dr. Samantha Meltzer-Brody?

Before a medication is approved for use, it must undergo rigorous clinical trials to make sure it is safe and effective.

Dr. Samantha Meltzer-Brody, director of the Center for Women’s Mood Disorders at UNC Chapel Hill, was one of the lead investigators for these studies. The experiments she led showed that the medication significantly reduced depressive symptoms.

Meltzer-Brody has also helped develop other PPD treatments.

Until now, the only widely available treatment for postpartum depression was an IV injection that had to be administered by a doctor or nurse. Meltzer-Brody helped lead clinical trials for this treatment, which later paved the way for its FDA approval.

She also developed a phone app called PPD Act, which helps postpartum women participate in studies that aim to create a better understanding of the disorder’s underlying genetic contributors.

The News & Observer honored her as a “Tar Heel of the Month” in 2019 for her contributions to the field of women’s mental health.

Teddy Rosenbluth covers science and health care for The News & Observer in a position funded by Duke Health and the Burroughs Wellcome Fund. The N&O maintains full editorial control of the work.

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This story was originally published August 5, 2023 at 1:22 PM.

Teddy Rosenbluth
The News & Observer
Teddy Rosenbluth covers science for The News & Observer in a position funded by Duke Health and the Burroughs Wellcome Fund. She has covered science and health care for Los Angeles Magazine, the Santa Monica Daily Press, and the Concord Monitor. Her investigative reporting has brought her everywhere from the streets of Los Angeles to the hospitals of New Delhi. She graduated from UCLA with a bachelor’s degree in psychobiology.
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