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Irritable Bowel SyndromePhase 2NCT03721107

A Trial for New Treatment of Adult Participants With Irritable Bowel Syndrome

A Phase 2 study testing Blautix in people with Irritable Bowel Syndrome, run by 4D pharma plc at 34 sites in 3 countries.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

Trial summary

A study to evaluate the effectiveness of oral doses of Blautix in adult participants with irritable bowel syndrome (IBS). Read more about this study

Who is it for?
Ages 18 to 70 years
Conditions the study is for
Irritable Bowel Syndrome
What is being tested?
Blautix
Type of treatment
Pill or oral medicine
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
366 participants
Where
34 sitesin 3 countries
Study dates
11 Oct 2018to 13 May 2020
Phase
Phase 2
Are there results?
Yes, posted in the registrySummary in the doctors' view

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 70 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Written consent on an Institutional Review Board (IRB)/ Independent Ethics Committee (IEC) approved informed consent form before any study specific evaluation
  • Males and Females between 18 and 70 years of age
  • Body Mass Index (BMI): 18-39 kg/m^2
  • Having IBS-C or IBS-D as defined by Rome IV* including Subtype Classification as defined in Table 2
  • Recurrent abdominal pain on average, at least 1 day/week in the last 3 months associated with two or more of the following criteria:
  • Related to defecation
Show all 12Show fewer
  • Associated with a change in frequency of stool
  • Associated with a change in form (appearance) of stool
  • Have a moderate or severe IBS symptom severity score (> 175) as defined by IBS-SSS
  • Table 2:
  • IBS -C Abdominal Pain Intensity: weekly average of worst daily (in past 24 hours) abdominal pain score of > 3.0 on a 0 to 10-point scale And Stool Frequency: more than 25% of bowel movements with a consistency of Type 1 or Type 2 Bristol stool chart and less than 25% of bowel movements with Bristol stool form Type 6 or Type 7. Participants must have fewer than 3 complete spontaneous bowel movements (CSBMs) within a one week period (7 days)
  • IBS-D Abdominal Pain Intensity: weekly average of worst daily (in past 24 hours) abdominal pain score of > 3.0 on a 0 to 10-point scale And Stool Consistency: more than 25% of bowel movements with a consistency of Type 6 or Type 7 Bristol stool chart and less than 25% of bowel movements with Bristol stool form Type 1 or Type 2.Participants must have at least one Type 6 or Type 7 bowel movements on at least four days within a one week period (7 days).

Who cannot join

  • Males or females <18 and >70 years of age
  • Have a IBS symptom severity score < 175 as defined by IBS-SSS
  • BMI: <18 or >39 kg/m^2
  • Have a significant acute or chronic coexisting illness (cardiovascular, gastrointestinal, endocrine, immunological, metabolic or any condition which contraindicates, in the investigators' judgment, entry to the study)
  • Confirmed clinical diagnosis of bile acid malabsorption and / or on medication for bile acid malabsorption
  • Individuals who, in the opinion of the investigator, are poor attendees or unlikely for any reason to be able to comply with the study requirements
Show all 26Show fewer
  • Participant is currently enrolled in or has not yet completed at least 30 days since ending other investigational device or drug study(s), or participant is receiving other investigational agent(s)
  • Have a malignant disease or any concomitant end-stage organ disease.
  • Females who are pregnant or breast feeding
  • Refusal to use acceptable methods of birth control (true abstinence, sterilisation, birth control pills, injections or contraceptive implants) for fertile participants (females) while on treatment and following completion of 2 menstrual cycles/ months after the last dose of study treatment. For Males, a barrier method of birth control from randomisation until the Follow-Up visit
  • Use of antibiotics within 1 month of screening
  • Use of systemic steroids within the last month
  • Change in dose or introduction of an antipsychotic within the last month
  • Have suffered from a major psychiatric disorder
  • Clinically diagnosed Lactose intolerance
  • Clinically diagnosed Coeliac disease
  • Change of diet e.g. FODMAP, gluten-free within last 3 months
  • Those > 50 will be excluded if their diagnosis of IBS is recent (<12 months) and if they have not had a sigmoidoscopy or colonoscopy within previous 5 years.
  • Any gastrointestinal-related abdominal surgery other than hernia repair or appendectomy
  • Participants taking prucalopride
  • Other investigational procedures while participating in this study are excluded
  • Known HIV infection, or hepatitis A, B, or C active infection
  • Participants with abnormal laboratory values at screening deemed by the investigator to be clinically significant
  • Participants who have taken commercially available probiotics within the last month (30 days prior to randomization)
  • Participants with known or suspected hereditary fructose intolerance, glucose-galactose malabsorption or sucrase-isomaltose insufficiency
  • Participants taking guanylate cyclase agonists, such as linaclotide and lubiprostone

Trial locations and contacts

34 sites in 3 countries.

34 sites in 3 countries

United States24 sites
  • Connecticut Gastroenterology Clinical Research

    Bristol, Connecticut, 06010

  • WR-ClinSearch

    Chattanooga, Tennessee, 37421

  • Aventiv Research Inc.

    Columbus, Ohio, 43213

  • Digestive CARE of North Broward, LLC

    Coral Springs, Florida, 33065

  • Evanston Premier Healthcare & Research, LLC.

    Evanston, Illinois, 60201

  • PharmQuest

    Greensboro, North Carolina, 27408

  • Houston Methodist Gastroenterology Associates

    Houston, Texas, 77030

  • Clinical Research Associates

    Huntsville, Alabama, 35801

  • Borland-Groover Clinic

    Jacksonville, Florida, 32256

  • Centex Research, Inc.

    Lake Charles, Louisiana, 70601

  • Blue Ridge Medical Research

    Lynchburg, Virginia, 24502

  • Clinical Neuroscience Solutions, Inc

    Memphis, Tennessee, 38119

  • Gulf Coast Medical Research, LLC.

    Missouri City, Texas, 77459

  • Coastal Carolina Research Center

    Mt. Pleasant, South Carolina, 29464

  • Translational Research Group, Inc

    North Hollywood, California, 91606

  • Orlando Florida BioClinica Research Network

    Orlando, Florida, 32806

  • Elite Clinical Studies

    Phoenix, Arizona, 85018

  • Clinical Research Center of Florida

    Pompano Beach, Florida, 33060

  • Probe Clinical Research

    Riverside, California, 92501

  • Capitol Research

    Rockville, Maryland, 20850

  • East Coast Institute for Research, LLC.

    Saint Augustine, Florida, 32086

  • Georgia Medical Associates

    Snellville, Georgia, 30078

  • Specialists in Gastroenterology

    St Louis, Missouri, 63141

  • Guardian Angel Research Center

    Tampa, Florida, 33614

Other trials in United States

United Kingdom9 sites
  • MAC Clinical Research (Barnsley)

    Barnsley, S75 3DL

  • MAC Clinical Research (Blackpool)

    Blackpool

  • MAC Clinical Research (Cannock)

    Cannock, WS11 0BN

  • CPS Research

    Glasgow, G20 0XA

  • MAC Clinical Research (Leeds)

    Leeds, LS10 1DU

  • MAC Clinical Research (Liverpool)

    Liverpool, L34 1BH

  • MAC Clinical Research (Manchester)

    Manchester, M13 9NQ

  • Wythenshawe Hospital

    Manchester, M23 9LT

  • MAC Clinical Research (Stockton-on-Tees)

    Stockton-on-Tees, TS17 6EW

Other trials in United Kingdom

Ireland1 site
  • Cork University Hospital

    Cork, T12 YE02

Other trials in Ireland

About this study

Official title: A Phase II Randomized, Double Blind, Placebo-controlled, Parallel Group, Multicenter Study to Evaluate the Safety and Efficacy of Repeated Oral Doses of Blautix in Adult Subjects With Irritable Bowel Syndrome (IBS) Subtypes IBS-C and IBS-D

A study to evaluate the effectiveness of oral doses of Blautix in adult participants with irritable bowel syndrome (IBS).

Read the detailed description

Participants with a diagnosis of IBS will be enrolled as defined by Rome IV criteria and will be classified into cohorts according to the Rome IV classification of IBS subtypes.

Each cohort (Cohort C and Cohort D) will recruit participants who will randomly receive either Blautix or matching placebo in a 1:1 ratio overall of treated to control participants.

Participants will undergo five visits in total across approximately 13 weeks. During the study treatment phase, participants will be asked to complete a variety of Quality of Life questionnaires at certain time points. These will consist of abdominal pain intensity score, IBS symptom severity (IBS-SSS), IBS quality of life (IBS-QoL), hospital anxiety and depression score (HADS), stool frequency, stool consistency \& food frequency questionnaire.

Participants will be required to produce relevant blood, urine and faecal samples at pre-determined timepoints from screening through to End of Treatment and follow up visits.

Being tested
Blautix, Placebo
Keywords
constipation, diarrhea
Medical subject headings
Irritable Bowel Syndrome, Constipation, Diarrhea

What participants receive

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

  • BlautixBiological

    Also called MRx1234, Blautia Hydrogenotrophica

    Blautix is a live biotherapeutic product consisting of a lyophilised formulation of a proprietary strain of bacterium. The study dosing regimen was two capsules two times per day for the duration of the treatment period.

  • PlaceboOther

    Placebo control

Study groups in NCT03721107
Study groupRoleWhat they receive
Cohort C: BlautixExperimentalParticipants diagnosed with Irritable bowel syndrome subtype C (IBS-C) received two capsules of Blautix orally, twice daily for 8 weeks. Maximum daily dose of Blautix (strain of Blautia hydrogenotrophica) will be 10^10 to10^11 most probable number (MPN).
Receives: Biological: Blautix
Cohort C: PlaceboPlacebo comparatorParticipants diagnosed with IBS-C received two capsules of placebo matched to Blautix orally, twice daily for 8 weeks.
Receives: Other: Placebo
Cohort D: BlautixExperimentalParticipants diagnosed with Irritable bowel syndrome subtype D (IBS-D) received two capsules of Blautix orally, twice daily for 8 weeks. Maximum daily dose of Blautix (strain of Blautia hydrogenotrophica) will be 10^10 to10^11 MPN.
Receives: Biological: Blautix
Cohort D PlaceboPlacebo comparatorParticipants diagnosed with IBS-D received two capsules of placebo matched to Blautix orally, twice daily for 8 weeks.
Receives: Other: Placebo

What is being measured

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

  1. Percentage of Participants With Overall Response

    Overall responder was a participant who has at least 7 evaluable weeks of data and has reported an improvement in their weekly symptoms (abdominal pain intensity [API] and stool frequency [SF] or consistency [SC]) for greater than or equal to (>=) 50 percent (%) of the treatment period. Improvement for abdominal pain intensity was defined as decrease in weekly average of worst abdominal pain in the past 24 hours score of at least 30% compared with baseline for Cohort C and Cohort D, for stool frequency was defined as increase of 1 or more complete spontaneous bowel movements (CSBM) per week compared with baseline for Cohort C and for stool consistency was defined as decrease at least 50% in the proportion of days per week with at least one stool that has a consistency of Type 6 or 7 compared with baseline for Cohort D. Participants with <4 weeks available were considered non-responders.

    Measured: Baseline up to Week 8

Secondary outcomes (8)
  1. Number of Participants With Treatment-Related Treatment-Emergent Adverse Events (TEAEs)

    An adverse event (AE) was any untoward medical occurrence in a participant administered study medication and which does not necessarily have a causal relationship with this treatment. A TEAE was defined as an AE that started or worsened in severity on or after the start date of the study treatment and includes all AEs recorded through the follow-up visit. A treatment-related TEAE was a TEAE possibly related to the study treatment.

    Measured: Baseline up to follow-up visit (up to Week 14)

  2. Number of Participants With Response to Subject Global Assessment of Relief

    The subject global assessment of relief was collected weekly through the electronic clinical outcome assessment (eCOA) system. It was a comparison of how the participant has felt over the past week with regards to their IBS to the way they felt before entering the study. It was measured on a 5-point Likert scale with the following responses: Completely relieved; considerably relieved; somewhat relieved; unchanged; worse. The total score ranged from 0-20, where higher scores indicated worsening of condition.

    Measured: Week 1, 4, 8, follow-up visit (Week 12, 13 and 14)

  3. Change in Percentage of Days Per Week With Undesired Stool Consistency From Baseline at Week 1, 4, 8, Follow-up Visit (Week 12, 13 and 14)

    Stool consistency of each bowel movement was rated on 7-level Bristol Stool Chart where Type 1 = separate hard lumps, like nuts (hard to pass), Type 2 = sausage-shaped but lumpy, Type 3 = like a sausage but with cracks on the surface, Type 4 = like a sausage or snake, smooth and soft, Type 5 = soft blobs with clear-cut edges (passed easily), Type 6 = fluffy pieces with ragged edges, a mushy stool, Type 7 = watery, no solid pieces; entirely liquid. A score range of 1 to 7 where, 1 or 2 indicates constipation and a score of 6 or 7 indicates diarrhea. Change in percentage of days per week with at least 1 stool with a undesired stool consistency of 1 or 2 for Cohort C and 6 or 7 for Cohort D on the Bristol Stool Chart from baseline at Week 1, 4, 8, Follow-up Visit (Week 12, 13 and 14) was reported.

    Measured: Baseline, Week 1, 4, 8, follow-up visit (Week 12, 13 and 14)

  4. Percent Change From Baseline in Stool Consistency Assessed by Bristol Stool Form Scale (BSFS) at Week 1, 4, 8, Follow-up Visit (Week 12, 13 and 14)

    Stool consistency of each bowel movement was assessed by participants using the 7-point BSFS from 1 to 7 where Type 1 = separate hard lumps, like nuts (hard to pass), Type 2 = sausage-shaped but lumpy, Type 3 = like a sausage but with cracks on the surface, Type 4 = like a sausage or snake, smooth and soft, Type 5 = soft blobs with clear-cut edges (passed easily), Type 6 = fluffy pieces with ragged edges, a mushy stool, Type 7 = watery, no solid pieces; entirely liquid. A score of 1 or 2 indicates constipation and a score of 6 or 7 indicates diarrhea. Lower numbers represented more formed stools and higher numbers represented less formed stools. A negative change from Baseline indicates improvement.

    Measured: Baseline, Week 1, 4, 8, follow-up visit (Week 12, 13 and 14)

  5. Change From Baseline in Weekly Average Stool Frequency Assessed by Bristol Stool Form Scale (BSFS) at Week 1, 4, 8, Follow-up Visit (Week 12, 13 and 14)

    Stool frequency was defined as a sum of weekly CSBMs. Participants were reminded to rate all their bowel movements in the Bristol Stool Chart (BSC) before answering the question. Stool types were assessed using the 7-point BSFS where 1 = separate hard lumps, like nuts (hard to pass), 2 = sausage-shaped but lumpy, 3 = like a sausage but with cracks on the surface, 4 = like a sausage or snake, smooth and soft, 5 = soft blobs with clear-cut edges (passed easily), 6 = fluffy pieces with ragged edges, a mushy stool, 7 = watery, no solid pieces; entirely liquid. A score of 1 or 2 indicates constipation and a score of 6 or 7 indicates diarrhea. Weekly stool frequency was based on the daily stool frequency which was calculated as follows: if there was 1 or more entry for BSC, the number of BSC entries was summed up. If on that day laxative was used, the daily stool frequency was set to 0. If an answer to CSBMs, but no BSC entry was provided, the daily stool frequency was set to 0 on that day.

    Measured: Baseline, Week 1, 4, 8, follow-up visit (Week 12, 13 and 14)

  6. Change From Baseline in IBS Quality of Life (IBS-QOL) Questionnaire Subscale and Total Scores at Week 4, 8 and Follow-up Visit (Weeks 12-14)

    Participants were asked to complete a QOL of 34 items which formed 8 scales: dysphoria (8 items), interference with activity (7 items), body image (4 items), health worry (3 items), food avoidance (3 items), social reaction (4 items), sexual (2 items), and relationships (3 items). All 8 scales were rated on a five-point response scale where, 1= not at all, 2= slightly, 3= moderately, 4= quite a bit, 5= extremely or a great deal. Scores for individual items were averaged to obtain a total score for each sub-scale of IBSQoL. Total and subscale scores were transformed to a 0 to 100 point scale (0=lowest score, 100=highest possible score) with higher scores indicating better IBS-specific quality of life. Transformed scale score = (Sum of the items-lowest possible score/Possible raw score range)∗100. A positive change from baseline indicates improved quality of life.

    Measured: Baseline, Week 4, 8, follow-up visit (Weeks 12-14)

  7. Change From Baseline in IBS Symptom Severity Score (IBS-SSS) at Week 4, 8 and Follow-up Visit (Weeks 12-14)

    Participants were asked to complete a questionnaire on the severity of abdominal distension and pain, frequency of abdominal pain, dissatisfaction with bowel habits, and interference of IBS symptoms with daily life. The IBS-SSS was measured on a Visual Analog Scale (VAS scale) in combination with reported numeric values which equated to an overall score. The scale range was from 0 (no symptoms) to 500 (maximum severity). Participants were categorized as having mild (74-174), moderate (175-299), or severe (>300) IBS symptoms based on symptomology. Higher scores were indicative of greater disease severity (worse outcome). A negative change from Baseline indicates improvement.

    Measured: Baseline, Week 4, 8, follow-up visit (Weeks 12-14)

  8. Change From Baseline in Hospital Anxiety and Depression (HADS) Total Score at Week 4, 8 and Follow-up Visit (Weeks 12-14)

    Participants were asked to complete the HADS which was a 14-item scale (7 items- anxiety and 7 items-depression) that generated ordinal data. Each question was rated on a scale from 0 - 3. The outcome of the HADS questionnaire was two total scores, the HADS-A (for anxiety) and the HADS-D (for depression). Both total scores are graded on a scale of 0 - 21 and can be categorized as Normal (0 - 7), Borderline Abnormal (8 - 10) and Abnormal (11 - 21). Higher scores indicate higher levels of anxiety and depression. A negative change from Baseline indicates improvement.

    Measured: Baseline, Week 4, 8, follow-up visit (Weeks 12-14)

Timeline

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

  1. First posted26 Oct 2018
  2. Study start11 Oct 2018
  3. Primary completion13 May 2020
  4. Study completion13 May 2020

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 2
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Double blind
Who is masked
Participant, Investigator
Enrolment
366 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03721107
Sponsor's protocol ID
BHT-II-002
Status last verified
Dec 2021
First submitted
1 Oct 2018
Last updated
11 Jan 2022
Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
Individual data sharing
No

Publications

  • Quigley EMM, Markinson L, Stevenson A, Treasure FP, Lacy BE. Randomised clinical trial: efficacy and safety of the live biotherapeutic product MRx1234 in patients with irritable bowel syndrome. Aliment Pharmacol Ther. 2023 Jan;57(1):81-93. doi: 10.1111/apt.17310. Epub 2022 Nov 11.

    PubMed 36369645

Questions about this trial

What is this clinical trial studying?

A Phase 2 study testing Blautix in people with Irritable Bowel Syndrome, run by 4D pharma plc at 34 sites in 3 countries.

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 12 inclusion and 26 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: finished, as of the sponsor's last update on 11 Jan 2022. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 34 sites in United States, United Kingdom, Ireland. 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.

What does this phase mean?

Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

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

Are results available for this study?

Yes. Results are posted in the registry (first posted 11 Jan 2022). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.

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

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Percentage of Participants With Overall Response (time frame: Baseline up to Week 8). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT03721107, which also lists 1 linked publication.

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 11 Jan 2022.

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