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DiarrheaPhase 4NCT07285785

Rifaximin 200 mg Plus Oral Rehydration vs Oral Rehydration Alone in Children With Acute Diarrhea

A Phase 4 study testing Rifaximin 200 mg Tablet and Oral Rehydration Therapy (ORT) in people with Diarrhea and Gastroenteritis, run by Bausch Health Americas, Inc. at 10 sites in United States.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
Search all trials

Trial summary

The goal of this clinical trial is to learn how rifaximin 200 mg is processed in the body (pharmacokinetics) in children 6 to 11 years old with acute diarrhea that may be caused by bacteria. Read more about this study

Who is it for?
Ages 6 to 12 years
Conditions the study is for
Diarrhea, Gastroenteritis, Bacterial Infection
What is being tested?
Rifaximin 200 mg Tablet and Oral Rehydration Therapy (ORT)
Type of treatment
Pill or oral medicine
Could I receive a placebo?
No, everyone receives an active treatment
How many people
54 participants
Where
10 sitesUnited States
Study dates
11 Feb 2026to 31 Jul 2027
Phase
Phase 4
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 6 to 12 years
  • All sexes
  • No healthy volunteers
  • Child

4.1 Inclusion Criteria

A participant will be eligible for inclusion in this study if all of the following criteria are met:

  1. Parent/legally authorized representative and participant, as applicable, have provided written informed consent/assent, are able to understand, and agree to comply with, all study procedures and requirements.
  2. Participant is between 6 to 11 years of age (inclusive)
  3. Participant weighs at least 15 kg (33 lbs) at Screening
  4. Participant is able to swallow pills
  5. Participant has diarrhea of suspected bacterial etiology defined by:
  6. At least 3 unformed stools in the last 24 hours prior to Screening
  7. Illness for less than 96 hours at Screening
  8. Clinical presentation consistent with acute infectious diarrhea of suspected bacterial etiology
  9. The participant agrees to use a highly effective method of contraception (if applicable) and to have urine pregnancy tests. Applies to females of childbearing potential (defined as postmenarche). Participants must practice at least 1 of the following medically acceptable methods of birth control throughout the study:

Applicable to:

All Post-Menarche Female Particpants:

  • Highly effective hormonal contraception methods such as oral, implantable, injectable, vaginal ring, or transdermal contraception for a minimum of 1 full cycle (based on the participant's usual menstrual cycle period) before study drug administration.
  • Total abstinence from sexual intercourse since the last menses before screening and agrees to total abstinence from screening until at least 30 days after last study drug administration.
  • Intrauterine device.

All Males Participants:

  • Condoms with spermicide.
  • Total abstinence from sexual intercourse from screening visit until at least 30 days after last study drug administration.

4.2 Exclusion Criteria

A participant will not be eligible for inclusion in this study if any of the following criteria are met:

  1. Participant has a history of chronic diarrhea (defined as loose or watery stools persisting for at last 4 consecutive weeks) within 12 months prior to onset of current acute illness.
  2. Participant is unable to eat or drink.
  3. Participant has clinical features suggestive of invasive or severe bacterial diarrhea requiring alternative therapy (e.g., frank blood in stool, mucoid diarrhea with systemic symptoms such as high fever, severe abdominal cramping or tenderness, or signs of sepsis).
  4. Participant has taken >2 doses of anti-diarrheal therapies in the 24 hours prior to randomization.
  5. Participant has taken any oral antimicrobial drug within 14 days of randomization.
  6. Participant has a clinically significant or unstable medical condition, in the opinion of the Investigator, (including, but not limited to, evidence of severe dehydration noted by tachycardia, abnormal blood pressure, or decreased skin turgor) at the Screening visit.
  7. Participant has a known hypersensitivity or allergy to Xifaxan®, rifampin, rifamycin-derived antibiotics, or any of the components of the rifaximin (Xifaxan®) formulations used in this study.
  8. Participant is pregnant or lactating or plans to become pregnant during the study.
  9. Participant has had a previous history of malignancy.
  10. Participant has a history of tuberculosis infection and/or has received treatment for tuberculosis infection.
  11. Participant has any concurrent illness, disability or circumstance that may affect the interpretation of clinical data, could cause noncompliance with treatment or visits or otherwise contraindicates participation in this study in the opinion of the Investigator.
  12. Participant has had significant blood loss within the 30 days prior to the Screening visit which prevents the collection of the blood volume required for this study.
  13. Participant has participated in an investigational drug or device study within the 30 days prior to randomization.
  14. Participant is an immediate household family member of study site personnel directly involved in the conduct of this study.
  15. Participant is taking a medication that is prohibited per Section 4.5 (Prohibited Therapy).

The following therapies are prohibited from Screening through Day 5:

  • Anti-diarrheal medications, including:
  • Anti-motility agents (eg, loperamide, diphenoxylate, codeine, and paregoric).
  • Absorbent agents (eg, cholestryramine).
  • Anti-secretory agents (eg, bismuth subsalicylate, octreotide, and vapreotide).
  • Probiotics
  • Any antimicrobial agents with an expected activity against enteric bacterial pathogens
  • A P-glycoprotein (P-gp) inhibitor
  • Warfarin

Trial locations and contacts

10 sites in 1 country. Contact the study team or a site near you to ask about taking part.

Maryanne Santilli contact

10 sites in 1 country

United States10 sites, 10 recruiting
  • Cyn3rgy Research Corporation

    Gresham, Oregon, 97030

    Primary Coordinator, 503-907-2179, dfranzen@cyn3rgy.com

    Frank Calgano

    Recruiting
  • Direct Helpers

    Hialeah, Florida, 33012

    Primary Coordinator, 305-828-3555, maria@dhrtrials.com

    Manuel Sanchez

    Recruiting
  • Innovative Clinical Research Center

    Island Lake, Illinois, 60042

    Primary Coordinator, 847-469-6971, abiola@icrcllc.com

    Eberechukwu Ibe

    Recruiting
  • Alliance Research Institute

    Lynwood, California, 90262

    Primary Coordinator, 310-933-8240, mreyes@allianceri.org

    James Saunders

    Recruiting
  • SouthCoast Research Center

    Miami, Florida, 33136

    Primary Coordinator, 786-332-2721, sc6@southresearch.org

    Adonis Maiquez

    Recruiting
  • Oceane7 Medical & Research Center, Inc

    Miami, Florida, 33144

    Primary Coordinator, 305-261-2738, c.aguiar.oceane7@gmail.com

    Edgar Gonzalez, MD

    Recruiting
  • Little Stars Pediatrics / Tattva Trials

    Prosper, Texas, 75078

    Primary Coordinator, 940-290-1949, a_Krishna@tattvatrials.com

    Pragadeeswari Dhanasekaran

    Recruiting
  • Tekton Research

    Richmond, Virginia, 23233

    Primary Coordinator, 804-430-5700, andy.afrifa@tektonresearch.com

    David Gosselin

    Recruiting
  • LinQ Research

    Rosharon, Texas, 77583

    Primary Coordinator, 281-916-4220, mustafa@linqresearchllc.com

    Frederick Ogwara

    Recruiting
  • Rophe Adult & Pediatric Medicine

    Union City, Georgia, 30291

    Primary Coordinator, 470-317-3604, nicole.williams@skycrng.com

    Yvonne Smith

    Recruiting

Other trials in United States

About this study

Official title: A Randomized, Open-Label Study to Assess Pharmacokinetics of Xifaxan® 200 mg in Pediatric Subjects 6 to 11 Years of Age With Acute Diarrhea of Suspected Bacterial Etiology, and the Safety and Efficacy of Xifaxan® 200 mg Plus Oral Rehydration Therapy (ORT) Compared to ORT Alone

The goal of this clinical trial is to learn how rifaximin 200 mg is processed in the body (pharmacokinetics) in children 6 to 11 years old with acute diarrhea that may be caused by bacteria. It will also learn about the safety and effectiveness of rifaximin when given with oral rehydration therapy (ORT) compared with ORT alone. The main questions it aims to answer are:

How does rifaximin 200 mg move through and leave the body in children with acute diarrhea?

Read more

Is rifaximin safe for children in this age group?

Does rifaximin plus ORT help resolve diarrhea faster than ORT alone?

Researchers will compare rifaximin plus ORT to ORT alone to see if adding rifaximin improves outcomes.

Participants will:

Take one rifaximin 200 mg tablet + ORT three times a day for 3 days or receive ORT alone

Receive oral rehydration therapy according to the investigator's standard of care

Attend up to 4 clinic visits over 5 days and receive 4 follow-up phone calls

Provide blood samples on Day 1 and Day 3 for pharmacokinetic testing (rifaximin group only)

Provide stool samples to identify bacterial pathogens

Keep a diary of stool frequency and consistency to help determine when diarrhea resolves

Be monitored for side effects, vital signs, and laboratory changes

Read the detailed description

This is a randomized, open-label study to assess the pharmacokinetics of Xifaxan® 200 mg in pediatric participants 6 to 11 years of age with acute diarrhea of suspected bacterial etiology, and safety and efficacy Xifaxan® 200 mg plus ORT compared to ORT alone.

Participants will receive Xifaxan® 200mg (1 tablet) TID plus oral rehydration therapy (ORT) or ORT alone as per the Investigator's Standard of Care (SOC) for administering ORS for three days.

Participants will complete 3 or 4 study visits during the study; Screening (Day -2 to Day 1), Day 1, Day 3 (End of Treatment), and Day 5 (Last Clinic Visit), and 2 safety follow-up phone calls; Once during Day 6 to 8, and on Day 30 (End of Study). Participants may complete both Screening and Day 1 on the same day. At the Screening visit, participants will provide a stool sample for PCR testing to identify the bacterial pathogen isolated. During the 5-day study period, the participant or their caregiver will complete a diary to record the dose, the time of dosing, time and consistency of stools, and incidence of symptoms as defined above. In addition, the participant or the caregiver will record any AEs in the eDiary from Day 4 to Day 30 with Day 1 to Day 3 assessed during study visits.

Participants in the Xifaxan® 200 mg plus ORT arm will undergo two 6 to 8-hour pharmacokinetic sampling periods, the first following the first dose on Day 1 and the second following the first dose on Day 3. During these sampling periods, 3 blood samples (approximately 4 mL each) will be collected for analysis of rifaximin and 25- desacetyl rifaximin plasma concentrations at the following times: pre-dose, 1 hour (+/- 10 minutes) and no less than 6 but no more than 8 hours following the first dose of the day.

Being tested
Rifaximin 200 mg Tablet, Oral Rehydration Therapy (ORT)
Keywords
pediatric, children, rifaximin, xifaxan, Oral Rehydration Therapy (ORT), acute diarrhea, bacterial diarrhea, gastroenteritis, open-label, randomized, ages 6-11, diarrhea
Medical subject headings
Diarrhea, Gastroenteritis, Bacterial Infections

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Rifaximin 200 mg TabletDrug

    Participants receive rifaximin 200 mg tablets orally three times daily (TID) for 3 days in combination with oral rehydration therapy (ORT). Blood samples for pharmacokinetic analysis are collected on Day 1 and Day 3 at pre-dose, 1 hour post-dose, and 6 to 8 hours post-dose.

  • Oral Rehydration Therapy (ORT)Other

    Participants receive oral rehydration solution according to the investigator's standard of care. This is administered either alone (for the ORT-alone arm) or in combination with rifaximin (for the rifaximin + ORT arm). Participants or caregivers complete a daily diary documenting stool frequency, stool consistency, and related symptoms.

Study groups in NCT07285785
Study groupRoleWhat they receive
Rifaximin 200 mg + ORTExperimentalrifaximin 200 mg tablets orally three times daily for 3 days plus oral rehydration therapy (ORT) administered per investigator standard of care
Receives: Drug: Rifaximin 200 mg Tablet; Other: Oral Rehydration Therapy (ORT)
ORT AloneActive comparatorORT administered per investigator standard of care without rifaximin.
Receives: Other: Oral Rehydration Therapy (ORT)

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Peak Plasma Concentration (Cmax) of Rifaximin

    Cmax levels following rifaximin 200 mg + ORT

    Measured: Days 1 and 3

  2. Time to Maximum Plasma Concentration (Tmax) of Rifaximin

    Tmax for rifaximin following rifaximin 200 mg + ORT

    Measured: Days 1 and 3

  3. Area Under the Plasma Concentration-Time Curve From Time 0 to Last Quantifiable Concentration (AUC0-last) for Rifaximin

    Area under the concentration-time curve to last measurable concentration

    Measured: Days 1 and 3

  4. Area Under the Plasma Concentration-Time Curve Over the Dosing Interval (AUC0-τ) for Rifaximin

    Area under the concentration-time curve over the dosing interval

    Measured: Days 1 and 3

  5. Proportion of participants with Clinical Cure

    Proportion of participants achieving clinical cure, defined as either:

    1. No unformed stools within a 48-hour period with no fever (with or without other clinical symptoms such as abdominal cramps or pain, excess gas/flatulence, nausea, vomiting, urgency, tenesmus); or
    2. No watery stools and no more than two soft stools within a 24-hour period with no fever and no other clinical symptoms except for mild excess gas/flatulence.

    Measured: Up to Day 5 (End of Treatment)

Secondary outcomes (4)
  1. Time to Last Unformed Stool (TLUS)

    Time in hours from the first dose of study treatment to the last unformed stool, after which clinical cure is declared, based on subject/caregiver diary entries.

    Measured: Up to Day 5 (End of Treatment)

  2. Incidence of Treatment-Emergent Adverse Events (AEs)

    Number and percentage of participants with AEs and SAEs

    Measured: Day 1-30

  3. Change From Baseline in Clinical Laboratory Parameters

    Changes in hematology, chemistry, and urinalysis values

    Measured: Day 1-30

  4. Change From Baseline in Vital Signs

    Change in temperature, blood pressure, and pulse

    Measured: Day 1-30

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted16 Dec 2025
  2. Study start11 Feb 2026
  3. Primary completion20 Apr 2027 (estimated)
  4. Study completion31 Jul 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 4
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
54 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07285785
Sponsor's protocol ID
RFPK1991
Status last verified
Aug 2026
First submitted
2 Dec 2025
Last updated
13 Aug 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
Yes
FDA-regulated device
No
Individual data sharing
No: The sponsor does not intend to share individual participant-level data from this study. Summary results will be posted in accordance with applicable regulations.

Questions about this trial

What is this clinical trial studying?

A Phase 4 study testing Rifaximin 200 mg Tablet and Oral Rehydration Therapy (ORT) in people with Diarrhea and Gastroenteritis, run by Bausch Health Americas, Inc. at 10 sites in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 13 Aug 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 10 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Angela Moore (843-877-2756, angela.moore@bauschhealth.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Peak Plasma Concentration (Cmax) of Rifaximin (time frame: Days 1 and 3). The study lists 5 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 13 Aug 2026.

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