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HealthyBioMet-7NCT07499414

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

A study testing 7-KLCA and Maltodextrin in people with Healthy, run by University of Reading at 1 site in United Kingdom.

Recruiting

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

Sites and contacts
Official record
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Trial 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. Read more about this study

Who is it for?
Ages 18 to 65 yearsHealthy volunteers can take part
Conditions the study is for
Healthy
What is being tested?
7-KLCA and Maltodextrin
Type of treatment
Pill or oral medicine
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
40 participants
Where
1 siteUnited Kingdom
Study dates
6 Apr 2026to 31 Dec 2027
Phase
Interventional
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 18 to 65 years
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • Volunteer is healthy (good physical and mental condition, disease-free, with haemoglobin 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 informed consent
  • 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

Who cannot join

  • 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
  • Clinically significant diabetes (plasma glucose test, fasting blood glucose > 6.5 mmol/l (120 mg/dL)
Show all 14Show fewer
  • 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

Trial locations and contacts

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

Abigail Basson, PhD contact

+44(0)7756872508

biomet-7@reading.ac.uk

Kimberly Watson, DPhil contact

+44(0)1183786640

biomet-7@reading.ac.uk

United Kingdom1 site, 1 recruiting
  • Hugh Sinclair Unit, Harry Nursten Building, University of Reading, Whiteknights Campus, RG6 6UR

    Reading

    Abigail Basson, PhD, +44(0)7756872508, biomet-7@reading.ac.uk

    Kimberly Watson, DPhil, +44(0)1183786640, biomet-7@reading.ac.uk

    Recruiting

Other trials in United Kingdom

About this study

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.

Conditions
Healthy
Being tested
7-KLCA, Maltodextrin
Keywords
gut microbiome, metabolic health, 7-KLCA, bile acid

What participants receive

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

  • 7-KLCADietary supplement

    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.

  • MaltodextrinDietary supplement

    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.

Study groups in NCT07499414
Study groupRoleWhat they receive
7-KLCAActive comparator7-KLCA intervention (400mg, taken once daily, in tablet form)
Receives: Dietary Supplement: 7-KLCA
MaltodextrinPlacebo comparatorMaltodextrin placebo (also in tablet form, taken once daily)
Receives: Dietary Supplement: Maltodextrin

What is being measured

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

  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).

    Measured: Baseline, Weeks 4, 12 and 16

Secondary outcomes (2)
  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.

    Measured: 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.

    Measured: Baseline, Weeks 4, 12 and 16

Timeline

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

  1. First posted30 Mar 2026
  2. Study start6 Apr 2026 (estimated)
  3. Primary completion5 Apr 2027 (estimated)
  4. Study completion31 Dec 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 N/A
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Masking
Double blind
Who is masked
Participant, Investigator
Enrolment
40 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07499414
Sponsor's protocol ID
BioMet-7
Acronym
BioMet-7
Status last verified
Mar 2026
First submitted
17 Mar 2026
Last updated
30 Mar 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing 7-KLCA and Maltodextrin in people with Healthy, run by University of Reading at 1 site in United Kingdom.

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

Who may be eligible to take part?

The sponsor lists 8 inclusion and 14 exclusion criteria. 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 30 Mar 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United Kingdom. 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. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

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 Abigail Basson, PhD (+44(0)7756872508, biomet-7@reading.ac.uk), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Gut Microbiome Composition (time frame: Baseline, Weeks 4, 12 and 16). 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 30 Mar 2026.

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