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Individualizing Anti-TNF Therapy in Patients With Inflammatory Bowel Disease

11 czerwca 2026 zaktualizowane przez: 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.

Przegląd badań

Szczegółowy opis

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.

Typ studiów

Obserwacyjny

Zapisy (Szacowany)

40

Kontakty i lokalizacje

Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.

Kontakt w sprawie studiów

Kopia zapasowa kontaktu do badania

Lokalizacje studiów

      • Tel Aviv, Izrael
        • Rekrutacyjny
        • Dep. of Gastroenterology, Tel Aviv Sourasky Medical Center
        • Kontakt:

Kryteria uczestnictwa

Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.

Kryteria kwalifikacji

Wiek uprawniający do nauki

  • Dorosły
  • Starszy dorosły

Akceptuje zdrowych ochotników

Nie

Metoda próbkowania

Próbka bez prawdopodobieństwa

Badana populacja

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

Opis

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

Plan studiów

Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.

Jak projektuje się badanie?

Szczegóły projektu

Kohorty i interwencje

Grupa / Kohorta
Interwencja / Leczenie
IBD patients
naïve to anti-TNF therapy
Patients will receive therapy as part of their standard care according to the standard dose
Inne nazwy:
  • Adalimumab (Humira)
  • Infliximab (Remicade)
  • Certolizumab pegol (Cimzia)
  • Golimumab (Simponi)

Co mierzy badanie?

Podstawowe miary wyniku

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

Miary wyników drugorzędnych

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

Współpracownicy i badacze

Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.

Śledczy

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

Daty zapisu na studia

Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.

Główne daty studiów

Rozpoczęcie studiów (Rzeczywisty)

4 stycznia 2025

Zakończenie podstawowe (Szacowany)

1 maja 2028

Ukończenie studiów (Szacowany)

1 grudnia 2028

Daty rejestracji na studia

Pierwszy przesłany

31 maja 2026

Pierwszy przesłany, który spełnia kryteria kontroli jakości

11 czerwca 2026

Pierwszy wysłany (Rzeczywisty)

12 czerwca 2026

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Rzeczywisty)

12 czerwca 2026

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

11 czerwca 2026

Ostatnia weryfikacja

1 maja 2026

Więcej informacji

Terminy związane z tym badaniem

Plan dla danych uczestnika indywidualnego (IPD)

Planujesz udostępniać dane poszczególnych uczestników (IPD)?

NIEZDECYDOWANY

Opis planu 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.

Informacje o lekach i urządzeniach, dokumenty badawcze

Bada produkt leczniczy regulowany przez amerykańską FDA

Nie

Bada produkt urządzenia regulowany przez amerykańską FDA

Nie

Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .

Badania kliniczne na Choroba Leśniowskiego-Crohna (CD)

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