ClinicalTrials.gg
RecruitingNCT07499414BioMet-7Updated Mar 30, 2026

The Effects of the Bile Acid Supplement, 7-keto Lithocholic Acid, on Human Gut Microbiota and Risk Factors for Disease.

An interventional study of 7-KLCA and Maltodextrin in Healthy, sponsored by University of Reading. Recruiting at 1 site in United Kingdom. Open to participants aged 18 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-03-30.

Sponsored by University of Reading · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
40
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
All
01

Study summary

In humans and most mammals, bile acids play a role in the metabolism of glucose and the transport and absorption of lipids (such as cholesterol and triglycerides), vitamins, and nutrients by allowing for emulsification (mixing) and absorption of fatty molecules that are consumed. More recently, bile acids have been discovered to influence the composition and quantity of the microorganisms in the gut microbiome. Bile acids also act as signalling molecules (like hormones) in the body, regulating important metabolic pathways and digestion.

While the majority of bile acids are recycled back to the liver, a small proportion of these bile acids enter the colon and interact with the gut microbiota. Primary bile acids, synthesized in the liver, are essential for the absorption of fat- and fat-soluble vitamins, as part of the digestive process. These primary bile acids are converted to secondary bile acids by gut bacteria, which have been shown to have benefits to health. This provides the rationale for exploring the use of a bile acid, in this case 7-keto lithocholic acid (7-KLCA), as a beneficial modulator of the gut microbiome, to help regulate metabolic and potentially other disease pathways.

Read the detailed description

Bile acids are small, naturally occurring molecules that play a vital role in the metabolism of glucose and lipids. Bile acids are classified as primary or secondary. Primary bile acids are made from cholesterol in the liver, where they form bile salts and are transported into the gall bladder before finally being secreted into the stomach, as part of the digestive process. \~95% of bile acids are recycled back to the liver, but a small proportion enters the colon and interacts with our gut microbiome. In the gut, these primary bile acids are converted to secondary bile acids (by our gut bacteria), and act as secondary signalling molecules that can affect health. Recent discoveries show that bile acids directly affect the gut microbiome. In fact, ursodeoxycholic acid (UDCA), a secondary bile acid, has a long history in medicine. Though currently used to treat liver diseases, treatment with UDCA has been found to increase the beneficial bacteria Faecalibacterium prausnitzii and reduce levels of hydrogen- and methane-producing bacteria in the gut. Therefore, there is potential to use UDCA (and UDCA-like molecules) as a prebiotic-like molecule that can be used by our gut microorganisms to promote beneficial bacteria in the gut and lead to a health benefit.

The bile acid 7-keto lithocholic acid (7-KLCA) is metabolised in the gut to produce UDCA. Using our in vitro fermentation models, UDCA and 7-KLCA were evaluated and found to increase the incidence of the beneficial microorganisms: Lactobacillus, Eubacterium rectale and Bifidobacterium spp. Changes in downstream bacterial metabolites and increases in short chain fatty acids also were observed. Our in vitro fermentation results, coupled with our in vitro cell culture studies, suggest there may be additional mechanisms by which UDCA and UDCA-like molecules exert their beneficial effects.

This study aims to assess in vivo, via a human intervention study, the prebiotic potential of 7-KLCA, as a bile acid supplement, and how microbial changes in the gut can improve biomarkers, indicative of beneficial metabolic and microbiome function and reduce risk factors of disease. In preparation for this study, 7-KLCA has undergone toxicology, absorption, and bioavailability studies to ensure it is safe for human consumption. Blood faecal and urine samples will be obtained at key points in the study, to assess microbial changes (bacterial count and composition, as well as metabolite profiling analysis; fatty acid, bile acid and lipids) and monitor key biomarkers (blood glucose and cholesterol, and indicators of inflammation and immune response), to address our primary and secondary research questions.

02

Conditions studied

  • Healthy

Keywords

  • gut microbiome
  • metabolic health
  • 7-KLCA
  • bile acid
03

In context

Lead sponsor

University of Reading is the lead sponsor of 150 studies on the registry; 21 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Volunteer is healthy (good physical and mental condition, disease-free, with levels between 138 - 172 g/L for male and between 121 and 151 g/L for female) at the time of pre-examination
  • Volunteer is aged ≥ 18 to ≤ 65 years for the duration of the study
  • Volunteer is able and willing to comply with the study instructions
  • Volunteer is suitable for participation in the study according to the investigator/study personnel
  • Volunteer is able to give
  • Volunteer must be following a non-restrictive diet according to the investigator/study personnel (no vegan, keto or fasting diets)
  • Volunteer has not consumed pro- or prebiotic supplements or food products for a minimum of 4 weeks prior to starting the intervention.
  • Volunteer has no gastrointestinal disorders

Exclusion criteria

Exclusion Criteria:

  • No command of any local language
  • Gastrointestinal disorders including IBS, IBD or other conditions that might affect the gut environment
  • Food allergies or intolerances
  • Using drugs (e.g. antibiotics) influencing gastrointestinal function (12 weeks before intervention)
  • Use of laxatives
  • diabetes (plasma glucose test, fasting blood glucose > 6.5 mmol/l (120 mg/dL)
  • Volunteers currently involved or will be involved in another clinical/ food study for the duration of this study
  • History of drug (pharmaceutical or recreational) or alcohol abuse.
  • If participants are pregnant or are lactating
  • Regular intake of probiotic or prebiotic supplements
  • Smoker
  • Those who follow extreme diets (Keto-diet, Atkins diet, vegan)
  • Those taking prescribed medication for existing health condition(s)
  • Those with a pacemaker
Terms in these criteria, in plain language(3)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Hemoglobin (Hb)

The protein in red blood cells that carries oxygen. A low level is anaemia, which can cause tiredness and breathlessness. Measured in g/dL or g/L (9 g/dL is 90 g/L).

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

Clinically significant

Judged by the study doctor to matter for your health or for the study. It is a doctor’s decision, so ask the study team if you are unsure whether something counts.

05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Investigator)
Enrollment
40 participants (estimated)

Study arms

  • Active comparator
    7-KLCA

    7-KLCA intervention (400mg, taken once daily, in tablet form)

    Dietary Supplement: 7-KLCA

  • Placebo comparator
    Maltodextrin

    Maltodextrin placebo (also in tablet form, taken once daily)

    Dietary Supplement: Maltodextrin

Interventions

  • Dietary supplement7-KLCA

    This study will be conducted as a 16 week duration parallel study. The trial will last for 112 days (16 weeks, includes a 1 month washout period and a follow up study visit to assess lasting effects) maximum, with participants assigned the intervention (400mg, taken once daily, 7-KLCA in tablet form) or maltodextrin placebo (also in matched tablet form) for 84 days.

  • Dietary supplementMaltodextrin

    This study will be conducted as a 16 week duration parallel study. The trial will last for 112 days (16 weeks, includes a 1 month washout period and a follow up study visit to assess lasting effects) maximum, with participants assigned the intervention (400mg, taken once daily, 7-KLCA in tablet form) or maltodextrin placebo (also in matched tablet form) for 84 days.

06

What researchers measure

Primary outcomes

  1. Gut Microbiome Composition

    Changes in microbial composition in stool will be measured by Flow-FISH to directly assess the benefits of 7-KLCA on modulating the gut microbiome (baseline, Weeks 4, 12, 16). 16s sequencing will be used to assess response to 7-KLCA before and after intervention (baseline and Week 12).

    Time frame: Baseline, Weeks 4, 12 and 16

Secondary outcomes

  1. Change in production of SCFA by the gut microbiota

    Gas chromatography will be used to analyse changes in SCFA content in stool to assess the activity of the gut microbiota as a result of 7-KLCA intervention.

    Time frame: Baseline, Weeks 4, 12 and 16

  2. Blood markers of health

    Fasting blood glucose, Hb1Ac (baseline and Week 12), blood lipids (total cholesterol, HDL, LDL, triglycerides), liver function (ALT, AST), kidney function (eGFR, creatnine), inflammatory markers (CRP, ESR) and immune markers (TNF-alpha, IL-6) will be measured to assess the benefits of 7-KLCA, which may help reduce the risk of developing disease.

    Time frame: Baseline, Weeks 4, 12 and 16

07

Study locations

1 of 1 sites recruiting
  • Hugh Sinclair Unit, Harry Nursten Building, University of Reading, Whiteknights Campus, RG6 6UR
    Reading, United Kingdom
    Recruiting
    • Abigail Basson, PhD · Contactbiomet-7@reading.ac.uk · +44(0)7756872508
    • Kimberly Watson, DPhil · Contactbiomet-7@reading.ac.uk · +44(0)1183786640
    • Kimberly Watson, DPhil · Principal investigator
    • Abigail Basson, PhD · Sub investigator
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for Apr 2026; primary completion for Apr 2027, 11 months later.

How these figures are worked out, and which studies are left out of them.

Registered
Mar 17, 2026
First posted
Mar 30, 2026
StartEst.
Apr 6, 2026
Primary completionEst.
Apr 5, 2027
CompletionEst.
Dec 31, 2027
Last update
Mar 30, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Mar 30, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07499414
Collaborators
ABC Farmaceutici S.p.A.
Responsible party
Kimberly Watson (Professor, University of Reading) — Principal investigator
First posted
Mar 30, 2026
Start date
Apr 6, 2026 (estimated)
Primary completion
Apr 5, 2027 (estimated)
Completion
Dec 31, 2027 (estimated)
Last update
Mar 30, 2026

Study contacts

Abigail Basson, PhD
Contact
biomet-7@reading.ac.uk
+44(0)7756872508
Kimberly Watson, DPhil
Contact
biomet-7@reading.ac.uk
+44(0)1183786640

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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