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IBD (Inflammatory Bowel Disease)NCT07644117

Individualizing Anti-TNF Therapy in Patients With Inflammatory Bowel Disease

An observational study of IBD (Inflammatory Bowel Disease) and Crohn Disease (CD), run by Shmuel Kivity, MD at 1 site in Israel.

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

This observational study aims to identify genes that may affect how patients with inflammatory bowel disease respond to anti-TNF treatment and why some patients lose response to treatment over time. Read more about this study

Who is it for?
Ages 18 years and older
How many people
40 participants
Where
1 siteIsrael
Study dates
4 Jan 2025to Dec 2028
How long will I take part?
52 Weeks
Phase
Observational
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 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Patients followed in the IBD unit in TLVMC starting or switching biologic therapy

Who may be able to join

  • Established IBD: Crohn's disease (CD) or ulcerative colitis (UC)
  • Anti-TNF naïve
  • Clinically active disease (HBI>5 for CD, p-MS≥ 3 for UC)
  • Elevated inflammatory indices CRP>10 or fecal calprotectin>250

Who cannot join

  • Unable to provide informed consent
  • Anti-TNF experienced
  • Unable to complete the study protocol

Trial locations and contacts

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

Rony Izhar, PhD contact

+97237772613

ronyi@tlvmc.gov.il

Ayal Hirsch, MD contact

+972535289492

ayalh@tlvmc.gov.il

Israel1 site, 1 recruiting
  • Dep. of Gastroenterology, Tel Aviv Sourasky Medical Center

    Tel Aviv

    Ayal Hirsch, MD, +972535289492, ayalh@tlvmc.gov.il

    Recruiting

Other trials in Israel

About this study

Official title: Individualizing Anti-TNF Therapy in Patients With Inflammatory Bowel Disease: Pre-Treatment Prediction of Immunogenicity and Response. A Prospective Observational Study.

This observational study aims to identify genes that may affect how patients with inflammatory bowel disease respond to anti-TNF treatment and why some patients lose response to treatment over time. The study will examine whether genetic markers can help predict which patients are more likely to respond to anti-TNF therapy.

Participants who have not previously received anti-TNF treatment and are about to start advanced therapy will provide a blood sample to test for the genetic markers. Participants will also undergo regular assessments of current treatment, disease activity, and inflammatory markers during follow-up.

Read the detailed description

The introduction of anti-TNF therapy was a pivotal milestone in the treatment of inflammatory bowel diseases (IBD). Since then, additional advanced therapies with novel mechanisms of action have been introduced. The plethora of biologics and small molecule drugs increases the ability of IBD patients to achieve therapeutic goals, such as clinical, endoscopic and mucosal healing. However, primary non-response and loss of response remain a challenge and are linked to increase risks related to ongoing inflammation and disease progression.

Predicting the response rates of individual patients to therapy is the goal of a large body of research, linked to clinical characteristics, genetics, microbiome composition and pharmacokinetics. Two promising research topics are Triggering Receptor Expressed in Myeloid cells 1 (TREM1) and HLA-DQA1*05.

TREM1 is a receptor expressed on innate immune cells, known to amplify inflammatory signals triggered by Toll-like receptors, thus contributing to the pathophysiology of acute and chronic inflammatory conditions. Increased protein and mRNA levels of TREM1 in whole blood and colonic biopsies are associated with clinical and endoscopic non-response to anti-TNF. The suggested best cut-off point is 3.346 folds increase in mRNA expression in whole blood samples, with a specificity of 91.3% and sensitivity of 58.1%.

HLA class II gene HLA-DQA1 is expressed by antigen presenting cells and encodes the α-chain of the HLA-DQ heterodimer that forms part of the antigen-binding site where epitopes are presented to T-helper cells. Carriage of HLA-DQA1*05 allele confers a 2-fold risk of immunogenicity to anti-TNF therapy. This risk was mitigated using a concomitant immunomodulator.

Our goal is to evaluate the predictive power of these tests separately in a prospective observational study, and assess whether combining the tests' outcomes prior to initiation of anti-TNF therapy improve therapy outcomes, including efficacy and durability.

The aims of this study are to assess the effectiveness of each test, and the combined tests for TREM1 and HLA-DQA1*05 to improve clinical and endoscopic response and remission rates, in patients with IBD starting anti-TNF therapy. The study will also assess the effectiveness of each test, and the combined tests for TREM1 and HLA-DQA1*05 in improving anti-TNF treatment durability and immunogenicity.

Participants will provide blood samples prior to treatment initiation for the assessment of HLA-DQA1*05 using quantitative real-time polymerase chain reaction (qRT-PCR) and TREM1 levels using an enzyme-linked immunosorbent assay (ELISA).

Drug and antibody levels will be measured at weeks 8, 24, and 52. Participants will also undergo periodic evaluations of their medical therapy and clinical disease activity throughout the study period.

Endoscopic disease activity (endoscopic MAYO score [eMAYO] for UC, and simple endoscopic score [SES-CD] for CD) will be evaluated with endoscopy 6-12 months after starting therapy, if performed as standard of care by the treating physician's discretion.

Statistical analysis Continuous variables will be presented as mean ± standard deviation for normal distribution and median with interquartile range for non-normal distribution. Nominal variables will be presented as proportions. Pearson correlation coefficient will be calculated to find association between HLA-DQA1*05 and anti-TNF immunogenicity, and between TREM1 expression and anti-TNF response rates. ROC curve with Youden index will be used to calculated area under the curve and optimal tests results predicting immunogenicity and response to therapy. Chi-Square test will be used to test the association between nominal variables. Comparison of continued variables groups will be performed by the independent samples t-test for variables which distribute normally, and by the Mann-Whitney test for variables which did not distribute normally. Normality will be tested graphically and using the Shapiro Wilk's test. Comparison of immunogenicity and response to therapy between study visits, and evaluation of the overtime trends in these parameters, in accordance with HLA-DQA1*05 and TREM1 tests results, will be performed by using the linear mixed model analysis (three or more visits) and by the paired sample T test (two visits). Statistical significance was set at P ≤ 0.05. All statistical analyses will be performed using R-4.3.2 for Windows.

Being tested
This is an observational study with no intervention. Patients will receive anti- TNF therapy as part of their standard care
Keywords
IBD, Anti-TNF, Response to treatment
Medical subject headings
Inflammatory Bowel Diseases, Crohn Disease, Colitis, Ulcerative

What participants receive

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

  • This is an observational study with no intervention. Patients will receive anti- TNF therapy as part of their standard careOther

    Also called Infliximab (Remicade), Adalimumab (Humira), Certolizumab pegol (Cimzia), Golimumab (Simponi)

    Patients will receive therapy as part of their standard care according to the standard dose

Study groups in NCT07644117
Study groupRoleWhat they receive
IBD patientsnaïve to anti-TNF therapy
Receives: Other: This is an observational study with no intervention. Patients will receive anti- TNF therapy as part of their standard care

What is being measured

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

  1. Rates of clinical response in UC patients

    Defined as decrease from baseline in partial Mayo score (p-MS) of ≥30%, plus a decrease in each sub score of ≥1.

    Measured: Week 8

  2. Rates of clinical response in UC patients

    Defined as decrease from baseline in partial Mayo score (p-MS) of ≥30%, plus a decrease in each sub score of ≥1.

    Measured: Week 24

  3. Rates of clinical response in UC patients

    Defined as decrease from baseline in partial Mayo score (p-MS) of ≥30%, plus a decrease in each sub score of ≥1.

    Measured: Week 52

  4. Rates of clinical response in CD patients

    Defined as decrease of at least 30% in Harvey-Bradshaw index (HBI).

    Measured: Week 8

  5. Rates of clinical response in CD patients

    Defined as decrease of at least 30% in Harvey-Bradshaw index (HBI).

    Measured: Week 24

  6. Rates of clinical response in CD patients

    Defined as decrease of at least 30% in Harvey-Bradshaw index (HBI).

    Measured: Week 52

  7. Rates of clinical remission for UC

    p-MS <3 and no sub score>1

    Measured: Week 8

  8. Rates of clinical remission for UC

    p-MS <3 and no sub score>1

    Measured: Week 24

  9. Rates of clinical remission for UC

    p-MS <3 and no sub score>1

    Measured: Week 52

  10. Rates of clinical remission for CD

    defined as HBI≤4

    Measured: Week 8

  11. Rates of clinical remission for CD

    defined as HBI≤4

    Measured: Week 24

  12. Rates of clinical remission for CD

    defined as HBI≤4

    Measured: Week 52

Secondary outcomes (17)
  1. c-reactive protein (CRP) levels

    Change from baseline in CRP levels

    Measured: Week 8

  2. CRP levels

    Change from baseline in CRP levels

    Measured: Week 24

  3. CRP levels

    Change from baseline in CRP levels

    Measured: Week 52

  4. Fecal calprotectin levels

    Change from baseline in fecal calprotectin levels

    Measured: Week 8

  5. Fecal calprotectin levels

    Change from baseline in fecal calprotectin levels

    Measured: Week 24

  6. Fecal calprotectin levels

    Change from baseline in fecal calprotectin levels

    Measured: Week 52

  7. Rates of endoscopic response for UC

    Endoscopic response defined as Mayo endoscopic sub-score (MES) ≤1

    Measured: Up to 12 months after initiating treatment

  8. Rates of endoscopic response for CD

    Endoscopic response defined as decrease in CDEIS>50%

    Measured: Up to 12 month after initiation of treatment

  9. Rates of endoscopic remission for UC

    defined as MES=0

    Measured: Up to 12 month after initiation of treatment

  10. Rates of endoscopic remission for CD

    defined as CDEIS<6 (CDEIS≤4 for isolated ileitis).

    Measured: Up to 12 month after initiation of treatment

  11. Immunogenicity

    anti-drug antibodies levels

    Measured: Week 8

  12. Immunogenicity

    anti-drug antibodies levels

    Measured: Week 24

  13. Immunogenicity

    anti-drug antibodies levels

    Measured: Week 52

  14. Drug levels

    Serum drug levels

    Measured: Week 8

  15. Drug levels

    Serum drug levels

    Measured: Week 24

  16. Drug levels

    Serum drug levels

    Measured: Week 52

  17. Therapeutic success

    Therapy persistence or discontinuation

    Measured: Through study completion, an average of 1 year

Timeline

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

  1. First posted12 Jun 2026
  2. Study start4 Jan 2025
  3. Primary completionMay 2028 (estimated)
  4. Study completionDec 2028 (estimated)

Resources

More details

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

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
40 participants (estimated)
Target duration
52 Weeks
IDs, dates and publications
ClinicalTrials.gov ID
NCT07644117
Sponsor's protocol ID
0156-TLV-GN
Status last verified
May 2026
First submitted
31 May 2026
Last updated
12 Jun 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided: At this time, there are no plans for data sharing or external collaborations. If data sharing is pursued in the future; only de-identified participant data will be shared, including demographic information, clinical indices and response to treatment.

Questions about this trial

What is this clinical trial studying?

An observational study of IBD (Inflammatory Bowel Disease) and Crohn Disease (CD), run by Shmuel Kivity, MD at 1 site in Israel.

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 4 inclusion and 3 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 12 Jun 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 Israel. 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.

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 Rony Izhar, PhD (+97237772613, ronyi@tlvmc.gov.il), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Rates of clinical response in UC patients (time frame: Week 8). The study lists 12 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 12 Jun 2026.

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