Diese Seite wurde automatisch übersetzt und die Genauigkeit der Übersetzung wird nicht garantiert. Bitte wende dich an die englische Version für einen Quelltext.

Individualizing Anti-TNF Therapy in Patients With Inflammatory Bowel Disease

11. Juni 2026 aktualisiert von: 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.

Studienübersicht

Detaillierte Beschreibung

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.

Studientyp

Beobachtungs

Einschreibung (Geschätzt)

40

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienkontakt

Studieren Sie die Kontaktsicherung

Studienorte

      • Tel Aviv, Israel
        • Rekrutierung
        • Dep. of Gastroenterology, Tel Aviv Sourasky Medical Center
        • Kontakt:

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

  • Erwachsene
  • Älterer Erwachsener

Akzeptiert gesunde Freiwillige

Nein

Probenahmeverfahren

Nicht-Wahrscheinlichkeitsprobe

Studienpopulation

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

Beschreibung

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

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

Kohorten und Interventionen

Gruppe / Kohorte
Intervention / Behandlung
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)

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Rates of clinical response in UC patients
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: Week 8
Defined as decrease of at least 30% in Harvey-Bradshaw index (HBI).
Week 8
Rates of clinical response in CD patients
Zeitfenster: Week 24
Defined as decrease of at least 30% in Harvey-Bradshaw index (HBI).
Week 24
Rates of clinical response in CD patients
Zeitfenster: Week 52
Defined as decrease of at least 30% in Harvey-Bradshaw index (HBI).
Week 52
Rates of clinical remission for UC
Zeitfenster: Week 8
p-MS <3 and no sub score>1
Week 8
Rates of clinical remission for UC
Zeitfenster: Week 24
p-MS <3 and no sub score>1
Week 24
Rates of clinical remission for UC
Zeitfenster: Week 52
p-MS <3 and no sub score>1
Week 52
Rates of clinical remission for CD
Zeitfenster: Week 8
defined as HBI≤4
Week 8
Rates of clinical remission for CD
Zeitfenster: Week 24
defined as HBI≤4
Week 24
Rates of clinical remission for CD
Zeitfenster: Week 52
defined as HBI≤4
Week 52

Sekundäre Ergebnismessungen

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

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Ermittler

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

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Tatsächlich)

4. Januar 2025

Primärer Abschluss (Geschätzt)

1. Mai 2028

Studienabschluss (Geschätzt)

1. Dezember 2028

Studienanmeldedaten

Zuerst eingereicht

31. Mai 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

11. Juni 2026

Zuerst gepostet (Tatsächlich)

12. Juni 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

12. Juni 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

11. Juni 2026

Zuletzt verifiziert

1. Mai 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Plan für individuelle Teilnehmerdaten (IPD)

Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?

UNENTSCHIEDEN

Beschreibung des IPD-Plans

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.

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Nein

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .

Klinische Studien zur Morbus Crohn (CD)

Abonnieren