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Individualizing Anti-TNF Therapy in Patients With Inflammatory Bowel Disease

11 giugno 2026 aggiornato da: 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.

Panoramica dello studio

Descrizione dettagliata

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.

Tipo di studio

Osservativo

Iscrizione (Stimato)

40

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Backup dei contatti dello studio

Luoghi di studio

      • Tel Aviv, Israele
        • Reclutamento
        • Dep. of Gastroenterology, Tel Aviv Sourasky Medical Center
        • Contatto:

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

No

Metodo di campionamento

Campione non probabilistico

Popolazione di studio

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

Descrizione

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

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

Coorti e interventi

Gruppo / Coorte
Intervento / Trattamento
IBD patients
naïve to anti-TNF therapy
Patients will receive therapy as part of their standard care according to the standard dose
Altri nomi:
  • Adalimumab (Humira)
  • Infliximab (Remicade)
  • Certolizumab pegol (Cimzia)
  • Golimumab (Simponi)

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Rates of clinical response in UC patients
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: Week 8
Defined as decrease of at least 30% in Harvey-Bradshaw index (HBI).
Week 8
Rates of clinical response in CD patients
Lasso di tempo: Week 24
Defined as decrease of at least 30% in Harvey-Bradshaw index (HBI).
Week 24
Rates of clinical response in CD patients
Lasso di tempo: Week 52
Defined as decrease of at least 30% in Harvey-Bradshaw index (HBI).
Week 52
Rates of clinical remission for UC
Lasso di tempo: Week 8
p-MS <3 and no sub score>1
Week 8
Rates of clinical remission for UC
Lasso di tempo: Week 24
p-MS <3 and no sub score>1
Week 24
Rates of clinical remission for UC
Lasso di tempo: Week 52
p-MS <3 and no sub score>1
Week 52
Rates of clinical remission for CD
Lasso di tempo: Week 8
defined as HBI≤4
Week 8
Rates of clinical remission for CD
Lasso di tempo: Week 24
defined as HBI≤4
Week 24
Rates of clinical remission for CD
Lasso di tempo: Week 52
defined as HBI≤4
Week 52

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
c-reactive protein (CRP) levels
Lasso di tempo: Week 8
Change from baseline in CRP levels
Week 8
CRP levels
Lasso di tempo: Week 24
Change from baseline in CRP levels
Week 24
CRP levels
Lasso di tempo: Week 52
Change from baseline in CRP levels
Week 52
Fecal calprotectin levels
Lasso di tempo: Week 8
Change from baseline in fecal calprotectin levels
Week 8
Fecal calprotectin levels
Lasso di tempo: Week 24
Change from baseline in fecal calprotectin levels
Week 24
Fecal calprotectin levels
Lasso di tempo: Week 52
Change from baseline in fecal calprotectin levels
Week 52
Rates of endoscopic response for UC
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: Week 8
anti-drug antibodies levels
Week 8
Immunogenicity
Lasso di tempo: Week 24
anti-drug antibodies levels
Week 24
Immunogenicity
Lasso di tempo: Week 52
anti-drug antibodies levels
Week 52
Drug levels
Lasso di tempo: Week 8
Serum drug levels
Week 8
Drug levels
Lasso di tempo: Week 24
Serum drug levels
Week 24
Drug levels
Lasso di tempo: Week 52
Serum drug levels
Week 52
Therapeutic success
Lasso di tempo: Through study completion, an average of 1 year
Therapy persistence or discontinuation
Through study completion, an average of 1 year

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Investigatori

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

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

4 gennaio 2025

Completamento primario (Stimato)

1 maggio 2028

Completamento dello studio (Stimato)

1 dicembre 2028

Date di iscrizione allo studio

Primo inviato

31 maggio 2026

Primo inviato che soddisfa i criteri di controllo qualità

11 giugno 2026

Primo Inserito (Effettivo)

12 giugno 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

12 giugno 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

11 giugno 2026

Ultimo verificato

1 maggio 2026

Maggiori informazioni

Termini relativi a questo studio

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

INDECISO

Descrizione del piano IPD

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.

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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