Efficacy of Rifaximin With NAC in IBS-D

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorMark Pimentel, MD

About this trial

The purpose of this study is to examine the effectiveness of using a combination of a drug, rifaximin and a dietary supplement, N-acetyl-L-cysteine (NAC), to treat patients with irritable bowel syndrome with diarrhea (IBS-D). Rifaximin is one of the standard treatments for IBS-D and is FDA approved. While rifaximin is safe and effective for treating symptoms in patients with IBS-D, many patients find that their symptoms may not completely resolve, or may come back after a period of time.

This research study is designed to test the investigational use of a combination of rifaximin and NAC. The combination of rifaximin and NAC is not approved by the U.S. Food and Drug Administration (FDA) for the treatment of IBS-D, and the effects of taking both medications together are unknown. However, the two medications are approved for use separately, as detailed below.

Rifaximin is the only antibiotic approved by the FDA for the treatment of IBS-D. Rifaximin (at a dose of 550 mg by mouth three times daily for 14 days) is approved by the FDA for the treatment of IBS-D. Rifaximin (at a dose of 200 mg per mouth three times daily for 3 days) is FDA approved for the treatment of traveler's diarrhea. Rifaximin at a dose of 200 mg per mouth three times daily is not approved by the FDA for the treatment of IBS-D.

NAC is approved by the FDA to treat acetaminophen overdose (72-hour oral and 21-hour intravenous (IV) regimens), and for use in breaking up mucus in the lungs in patients with chronic obstructive pulmonary disease (COPD) and other lung conditions such as bronchitis. NAC is also available over-the-counter in 600 mg and 900 mg capsules as a dietary supplement, although over-the-counter use is not regulated by the FDA. This study will utilize the 600 mg dietary supplement capsules.

The Investigators want to know if using a combination of rifaximin and NAC will give better results in decreasing IBS-D symptoms than using rifaximin alone. As NAC is used to break up mucus in the lungs, and the Investigators want to see if this can also break up the mucus layer in the small intestine, and therefore potentially increase the effectiveness of rifaximin. The Investigators will be testing 2 doses to determine which dose is most effective.

participants are being asked to take part in this research study because participants were diagnosed with IBS-D.

Eligibility criteria

Qualifiers

Male or non-pregnant, non-lactating female patients ≥ 18 years of age

Diagnosed with IBS confirmed by the Rome IV criteria, with associated symptoms of diarrhea as noted below in 4(b).

Do not have adequate relief of IBS symptoms of abdominal pain, stool consistency or stool frequency

Weekly average score of worst daily abdominal pain >3.0 on a 0-10 point scale

Disqualifiers

Less than 3 bowel movements a week,

Hard or lumpy stools, and

Excessive straining during a bowel movement.

History of inflammatory bowel disease, celiac disease, GI surgery (except cholecystectomy and/or appendectomy)

Trial design

Treatments tested in this trial

  • rifaximin 66mg + N-acetylcysteine 560mg three times daily
  • RNIB21 containing rifaximin 132mg + N-acetylcysteine 560mg three times daily
  • Placebo

Treatment groups

225 Participants
are divided into 3 treatment groups

Sponsors and collaborators

Mark Pimentel, MD

Lead sponsor

Cedars-Sinai Medical Center

Sponsor institution