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

2026年9月17日 更新者: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.

調査の概要

研究の種類

介入

入学 (推定)

240

段階

  • フェーズ 4

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

研究場所

      • Clermont-Ferrand、フランス
      • La Roche-sur-Yon、フランス
        • CHD de Vendée
      • Montpellier、フランス、34000

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 大人
  • 高齢者

健康ボランティアの受け入れ

いいえ

説明

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

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的:Time to efficacy (1: infliximab 2: filgotinib 3: ustekinumab 4: vedolizumab)
Follow the processing sequence based on time to efficacy.
実験的:Safety profile (1: ustekinumab 2: vedolizumab 3: infliximab 4: filgotinib)
Follow the processing sequence based on safety.
実験的:French current use* (1: vedolizumab 2: infliximab 3: filgotinib 4: ustekinumab)
Follow the processing sequence based on French current use.
実験的:Convenience (1: filgotinib 2: ustekinumab 3: vedolizumab 4: infliximab)
Follow the processing sequence based on convenience.

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Clinical remission
時間枠: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.

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

捜査官

  • 主任研究者:Anthony Buisson、University Hospital, Clermont-Ferrand

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2026年12月1日

一次修了 (推定)

2030年6月1日

研究の完了 (推定)

2030年12月1日

試験登録日

最初に提出

2026年5月4日

QC基準を満たした最初の提出物

2026年5月4日

最初の投稿 (実際)

2026年5月8日

学習記録の更新

投稿された最後の更新 (実際)

2026年9月18日

QC基準を満たした最後の更新が送信されました

2026年9月17日

最終確認日

2026年3月1日

詳しくは

本研究に関する用語

その他の研究ID番号

  • PHRC N 2020 BUISSON (STARTER)
  • 2024-514964-24-00 (その他の識別子:2024-514964-24-00)

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

いいえ

医薬品およびデバイス情報、研究文書

米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

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