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FirST Lines of Biologics in pAtients With ulceRaTivE Colitis: a Randomised Controlled Trial (STARTER)

17 de setembro de 2026 atualizado por: University Hospital, Clermont-Ferrand

Ulcerative colitis (UC) is a chronic bowel disease. It causes inflammation of the rectum and sometimes the colon. This disease can also affect other parts of the body. It can be very difficult to live with on a daily basis. People with UC may experience frequent diarrhea, rectal bleeding, urgency to defecate, and even incontinence. All of this can significantly reduce their quality of life.

The goal of treatment is twofold:

  • To eliminate or reduce symptoms (this is clinical remission),
  • To allow the bowel to heal.

When these two goals are achieved, the risk of relapse, hospitalization, surgery, or colorectal cancer decreases.

To monitor the progression of the disease, gastroenterologists use a test called fecal calprotectin: this is a protein measured in stool that helps detect intestinal inflammation.

When conventional treatments like corticosteroids or immunosuppressants are ineffective or poorly tolerated, the investigators use more targeted therapies.

For a long time, doctors have used drugs called anti-TNFs. They block a protein responsible for inflammation (TNF-alpha). These treatments are often injected under the skin, which is generally well-tolerated by patients.

A drug called infliximab, now available as a subcutaneous injection, could be used as a first-line treatment for ulcerative colitis because it appears to be more effective than other injectable anti-TNFs.

Another drug, vedolizumab, works differently from anti-TNFs and can also be used as a first-line treatment.

More recently, new classes of drugs have shown promise:

  • JAK inhibitors (such as filgotinib),
  • interleukin-12 and interleukin-23 inhibitors (such as ustekinumab).

These new treatments have advantages, such as the oral administration method for filgotinib and the fact that they can be used alone, without any other associated medication, which could simplify patients' lives and improve their quality of life.

Today, there are increasingly more different treatments for ulcerative colitis, and the investigators still don't know clearly what the best strategy is:

Is it better to start with one type of medication rather than another? Does the order in which the investigators try treatments lead to different results?

This is an important question for gastroenterologists, as their goal is to choose the most appropriate treatment for each patient from the outset.

The main objective of this research is to compare four strategies, corresponding to four treatment arms, starting with the use of infliximab, filgotinib, vedolizumab, or ustekinumab, to maintain remission in patients with ulcerative colitis.

The following four arms are therefore proposed:

  • Based on efficacy: infliximab - filgotinib - ustekinumab - vedolizumab
  • Based on safety: ustekinumab - vedolizumab - infliximab - filgotinib
  • Based on current practice: vedolizumab - infliximab - filgotinib - ustekinumab
  • Based on convenience and route of administration: filgotinib - ustekinumab - vedolizumab - infliximab

This study will also allow for a comparison of the efficacy, safety, participant acceptability, and quality of life of the four treatment regimens.

This study is intended for adult patients (aged 18 to 65), male or female, with moderate or severe ulcerative colitis (UC) for at least 3 months. Treatment for these patients must require biologic therapy, as determined by the investigator. Participants must be able to provide informed consent to participate in the research and must be covered by a national health insurance plan. Women of childbearing age must be using active contraception for at least the duration of the study (2 years).

Patients will be followed for two years. They will be seen at the initial visit, then every two months during the first year, and then every three months during the second year. At each visit, they will be required to undergo blood and stool tests and complete a questionnaire. Endoscopies will be scheduled for weeks 16, 52, and 104. Patient treatments can be optimized once, and based on the endoscopic score, patients may change treatments according to a predefined sequence.

Visão geral do estudo

Tipo de estudo

Intervencional

Inscrição (Estimado)

240

Estágio

  • Fase 4

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Contato de estudo

Locais de estudo

      • Clermont-Ferrand, França
      • La Roche-sur-Yon, França
        • CHD de Vendée
      • Montpellier, França, 34000

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Adulto
  • Adulto mais velho

Aceita Voluntários Saudáveis

Não

Descrição

Inclusion Criteria:

  • Male or female patients (using effective contraception and a negative pregnancy test for women of childbearing age) diagnosed with UC for at least 3 months
  • Age ≥ 18 years and ≤ 65 years
  • Moderate to severe UC according to modified Mayo score (from 5 to 9)
  • With endoscopic Mayo score ≥ 2
  • With an inadequate response, failure, loss of response, or intolerance to 5-ASA, steroids, or immunosuppressants.
  • Patient capable of giving consent
  • Patient covered by the French healthcare system
  • Women of childbearing age using active contraception (contraceptive implant, oral contraception, female condom or abstinence)) for at least the duration of the study

Exclusion Criteria:

  • Usual contra-indication to infliximab, filgotinib, vedolizumab or ustekinumab
  • Steroids > 20 mg/day within two weeks before inclusion
  • Low proctitis (disease limited to the rectum with an extent < 5 cm)
  • Prior history of thromboembolism events
  • Prior history of major cardiovascular problems (such as heart attack or stroke)
  • Long-standing smokers (> 40 pack years)
  • Crohn's disease
  • Stoma or colectomy
  • Prior exposure to anti-TNF agents, anti-integrins, anti-interleukines 12 and 23 or JAK inhibitor
  • Prior exposure to other biologics or experimental drug
  • No health insurance
  • Pregnant or lactating women : a pregnancy test will be performed for women of childbearing age
  • Patients already included in biomedical research other than an observational study (e.g: registry, cohort)
  • Concomitant Clostridioides difficile infection
  • HIV infection
  • Patient who does not master the French language
  • Patient under guardianship, curatorship or safeguard of justice
  • Minors

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Tratamento
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: Time to efficacy (1: infliximab 2: filgotinib 3: ustekinumab 4: vedolizumab)
Follow the processing sequence based on time to efficacy.
Experimental: Safety profile (1: ustekinumab 2: vedolizumab 3: infliximab 4: filgotinib)
Follow the processing sequence based on safety.
Experimental: French current use* (1: vedolizumab 2: infliximab 3: filgotinib 4: ustekinumab)
Follow the processing sequence based on French current use.
Experimental: Convenience (1: filgotinib 2: ustekinumab 3: vedolizumab 4: infliximab)
Follow the processing sequence based on convenience.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Clinical remission
Prazo: Remission will be assessed as a binary criterion (yes/no) each month (i.e. 4 weeks-period) between week 4 and week 52, the month being considered as the statistical unit and not the patient.
Remission (composite criteria) = no rectal bleeding, normalization of bowel habits (Mayo sub-score of stool frequency = 0) AND faecal calprotectin < 150 µg/g AND no steroids.
Remission will be assessed as a binary criterion (yes/no) each month (i.e. 4 weeks-period) between week 4 and week 52, the month being considered as the statistical unit and not the patient.

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Investigadores

  • Investigador principal: Anthony Buisson, University Hospital, Clermont-Ferrand

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Estimado)

1 de dezembro de 2026

Conclusão Primária (Estimado)

1 de junho de 2030

Conclusão do estudo (Estimado)

1 de dezembro de 2030

Datas de inscrição no estudo

Enviado pela primeira vez

4 de maio de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

4 de maio de 2026

Primeira postagem (Real)

8 de maio de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

18 de setembro de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

17 de setembro de 2026

Última verificação

1 de março de 2026

Mais Informações

Termos relacionados a este estudo

Outros números de identificação do estudo

  • PHRC N 2020 BUISSON (STARTER)
  • 2024-514964-24-00 (Outro identificador: 2024-514964-24-00)

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

NÃO

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

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