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Individualizing Anti-TNF Therapy in Patients With Inflammatory Bowel Disease

11 juni 2026 bijgewerkt door: Shmuel Kivity, MD

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.

Studie Overzicht

Gedetailleerde beschrijving

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.

Studietype

Observationeel

Inschrijving (Geschat)

40

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studiecontact

Studie Contact Back-up

Studie Locaties

      • Tel Aviv, Israël
        • Werving
        • Dep. of Gastroenterology, Tel Aviv Sourasky Medical Center
        • Contact:

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

  • Volwassen
  • Oudere volwassene

Accepteert gezonde vrijwilligers

Nee

Bemonsteringsmethode

Niet-waarschijnlijkheidssteekproef

Studie Bevolking

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

Beschrijving

Inclusion Criteria:

  • 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

Exclusion Criteria:

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

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

Cohorten en interventies

Groep / Cohort
Interventie / Behandeling
IBD patients
naïve to anti-TNF therapy
Patients will receive therapy as part of their standard care according to the standard dose
Andere namen:
  • Adalimumab (Humira)
  • Infliximab (Remicade)
  • Certolizumab pegol (Cimzia)
  • Golimumab (Simponi)

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Rates of clinical response in UC patients
Tijdsspanne: Week 8
Defined as decrease from baseline in partial Mayo score (p-MS) of ≥30%, plus a decrease in each sub score of ≥1.
Week 8
Rates of clinical response in UC patients
Tijdsspanne: Week 24
Defined as decrease from baseline in partial Mayo score (p-MS) of ≥30%, plus a decrease in each sub score of ≥1.
Week 24
Rates of clinical response in UC patients
Tijdsspanne: Week 52
Defined as decrease from baseline in partial Mayo score (p-MS) of ≥30%, plus a decrease in each sub score of ≥1.
Week 52
Rates of clinical response in CD patients
Tijdsspanne: Week 8
Defined as decrease of at least 30% in Harvey-Bradshaw index (HBI).
Week 8
Rates of clinical response in CD patients
Tijdsspanne: Week 24
Defined as decrease of at least 30% in Harvey-Bradshaw index (HBI).
Week 24
Rates of clinical response in CD patients
Tijdsspanne: Week 52
Defined as decrease of at least 30% in Harvey-Bradshaw index (HBI).
Week 52
Rates of clinical remission for UC
Tijdsspanne: Week 8
p-MS <3 and no sub score>1
Week 8
Rates of clinical remission for UC
Tijdsspanne: Week 24
p-MS <3 and no sub score>1
Week 24
Rates of clinical remission for UC
Tijdsspanne: Week 52
p-MS <3 and no sub score>1
Week 52
Rates of clinical remission for CD
Tijdsspanne: Week 8
defined as HBI≤4
Week 8
Rates of clinical remission for CD
Tijdsspanne: Week 24
defined as HBI≤4
Week 24
Rates of clinical remission for CD
Tijdsspanne: Week 52
defined as HBI≤4
Week 52

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
c-reactive protein (CRP) levels
Tijdsspanne: Week 8
Change from baseline in CRP levels
Week 8
CRP levels
Tijdsspanne: Week 24
Change from baseline in CRP levels
Week 24
CRP levels
Tijdsspanne: Week 52
Change from baseline in CRP levels
Week 52
Fecal calprotectin levels
Tijdsspanne: Week 8
Change from baseline in fecal calprotectin levels
Week 8
Fecal calprotectin levels
Tijdsspanne: Week 24
Change from baseline in fecal calprotectin levels
Week 24
Fecal calprotectin levels
Tijdsspanne: Week 52
Change from baseline in fecal calprotectin levels
Week 52
Rates of endoscopic response for UC
Tijdsspanne: Up to 12 months after initiating treatment
Endoscopic response defined as Mayo endoscopic sub-score (MES) ≤1
Up to 12 months after initiating treatment
Rates of endoscopic response for CD
Tijdsspanne: Up to 12 month after initiation of treatment
Endoscopic response defined as decrease in CDEIS>50%
Up to 12 month after initiation of treatment
Rates of endoscopic remission for UC
Tijdsspanne: Up to 12 month after initiation of treatment
defined as MES=0
Up to 12 month after initiation of treatment
Rates of endoscopic remission for CD
Tijdsspanne: Up to 12 month after initiation of treatment
defined as CDEIS<6 (CDEIS≤4 for isolated ileitis).
Up to 12 month after initiation of treatment
Immunogenicity
Tijdsspanne: Week 8
anti-drug antibodies levels
Week 8
Immunogenicity
Tijdsspanne: Week 24
anti-drug antibodies levels
Week 24
Immunogenicity
Tijdsspanne: Week 52
anti-drug antibodies levels
Week 52
Drug levels
Tijdsspanne: Week 8
Serum drug levels
Week 8
Drug levels
Tijdsspanne: Week 24
Serum drug levels
Week 24
Drug levels
Tijdsspanne: Week 52
Serum drug levels
Week 52
Therapeutic success
Tijdsspanne: Through study completion, an average of 1 year
Therapy persistence or discontinuation
Through study completion, an average of 1 year

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Onderzoekers

  • Hoofdonderzoeker: Ayal Hirsch, MD, Tel Aviv Sourasky University Medical Center

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Werkelijk)

4 januari 2025

Primaire voltooiing (Geschat)

1 mei 2028

Studie voltooiing (Geschat)

1 december 2028

Studieregistratiedata

Eerst ingediend

31 mei 2026

Eerst ingediend dat voldeed aan de QC-criteria

11 juni 2026

Eerst geplaatst (Werkelijk)

12 juni 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

12 juni 2026

Laatste update ingediend die voldeed aan QC-criteria

11 juni 2026

Laatst geverifieerd

1 mei 2026

Meer informatie

Termen gerelateerd aan deze studie

Plan Individuele Deelnemersgegevens (IPD)

Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?

ONBESLIST

Beschrijving IPD-plan

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.

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Nee

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .

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