FDA approved a 1st-of-its-kind treatment made from human poop. What does it do?

For the first time, the Food and Drug Administration (FDA) has approved a treatment that's made using donated human poop, the agency announced (opens in new tab) Wednesday (Nov. 30). The treatment, called Rebyota, contains gut bacteria collected from the stool of healthy human donors and is approved for the prevention of a potentially life-threatening bacterial infection. 

By administering the liquid treatment into a patient's rectum through a tube, doctors can help restore balance to the patient's gut microbiome, the community of microbes living in the lower digestive tract. 

Rebyota is approved for use in people ages 18 and older who have recently been treated for recurrent infections with the bacterium Clostridioides difficile, commonly called C. diff for short. C. diff can rapidly take over the gut if the normal microbiome gets disrupted — for example, as a result of antibiotic use. People aged 65 and older, those with weakened immune systems and those who have recently stayed in a hospital or nursing home face the highest risk of infection. As C. diff multiplies in the gut, the bacteria release toxins that trigger diarrhea, abdominal pain, fever and inflammation of the colon (colitis). Sometimes, the infections can lead to organ failure and even death, according to the FDA.

C. diff is estimated to cause about half a million infections in the U.S. each year, and about 1 in 6 patients who develop the infection will get it again within two to eight weeks of recovering, according to the Centers for Disease Control and Prevention (opens in new tab).

Related: 'Poop pills' work just as well as traditional fecal transplants

These recurrent infections can be treated with antibiotics, but the drugs don't always work against aggressive, antibiotic-resistant strains of C. diff, and what's more, they can further disrupt the microbiome and sometimes worsen the infection, according to The Scientist (opens in new tab). To get at the root cause of the problem — the unbalanced gut microbiome — doctors have increasingly turned to so-called fecal microbiota transplants. 

Previously considered an "investigational" treatment by the FDA, these transplants involve transferring screened donor stool into the patient's gut via a colonoscopy, enema or pill. However, sourcing and screening the stool presents a challenge, meaning the transplants haven't been readily available everywhere, and the lack of an FDA-approved product means the therapy often hasn't been covered by insurance, The Scientist reported.

—Why is poop brown?

—Cancer patients weren't responding to therapy. Then they got a poop transplant.

—The same exact foods affect each person's gut bacteria differently 

But now, Rebyota is available as the first FDA-approved "fecal microbiota product." In a late-stage clinical trial, the one-dose treatment reduced the rate of C. diff flare-ups by 29.4% in the eight weeks after antibiotic treatment, compared with a placebo, STAT reported (opens in new tab). Taking two clinical trials of the treatment into account, the success rate of the treatment "was significantly higher in the Rebyota group (70.6%) than in the placebo group (57.5%)," the FDA noted.

"Today's approval of Rebyota is an advance in caring for patients who have recurrent C. difficile infection [CDI]," Dr. Peter Marks (opens in new tab), director of the FDA's Center for Biologics Evaluation and Research, said in the agency's statement. "As the first FDA-approved fecal microbiota product, today’s action represents an important milestone, as it provides an additional approved option to prevent recurrent CDI."

In clinical trials, the most common side effects of Rebyota were abdominal pain, diarrhea, abdominal bloating, gas and nausea. And although the donated feces is carefully screened for pathogens, the treatment does carry some risk of transmitting infectious agents, and it may also contain food allergens, the FDA noted. "The potential for the product to cause adverse reactions due to food allergens is unknown," the agency's statement reads.