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Efficacy of Upadacitinib Re-induction Therapy in Patients With Ulcerative Colitis Who Lost Response to 30 mg Maintenance Dose (ReCOUP)

A Single Arm, Multicenter Open-Label Interventional to Evaluate the Efficacy of Upadacitinib Re-induction Therapy in Patients With Ulcerative Colitis Who Lost Response to 30 mg Maintenance Dose

ReCOUP is a multicenter clinical study designed to evaluate the efficacy of upadacitinib (Rinvoq®) in patients with ulcerative colitis whose disease has become active again despite maintenance treatment with upadacitinib 30 mg.

This study involves adult patients aged 18 to 64 years with active ulcerative colitis, who are being treated with upadacitinib and are not participating in another interventional clinical trial.

Participation in this study will depend on the patients' response to treatment during the 52-week maintenance period.

Several follow-up visits will be scheduled throughout the study according to a timetable defined by the protocol, and additional visits may be arranged if necessary depending on patients' health status.

研究概览

地位

尚未招聘

研究类型

介入性

注册 (估计的)

100

阶段

  • 第四阶段

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

  • 姓名:Project Director Getaid
  • 电话号码:+33 (0)9 72 57 61 60
  • 邮箱:jmussot@getaid.org

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人

接受健康志愿者

不

描述

Inclusion Criteria:

  1. Subjects must voluntarily sign and date an informed consent, approved by an IEC/IRB, prior to the initiation of any screening or study-specific procedures.
  2. Individuals at least 18 years old and less than 65 years.
  3. Laboratory values meeting the following criteria within the screening period prior to the first dose of study drug:

    • Serum alanine transaminase (ALT) < 2 × ULN;
    • Serum aspartate aminotransferase (AST) < 2 x ULN;
    • Estimated glomerular filtration rate (GFR) by simplified 4-variable Modification of Diet in Renal Disease (MDRD) formula > 0 mL/min/1.73 m2;
    • Total white blood cell (WBC) count > 2,500/μL;
    • Absolute neutrophil count (ANC) > 1,500/μL;
    • Platelet count > 100,000/μL;
    • Absolute lymphocyte count > 850/μL;
    • Hemoglobin > 10 g/dL.
  4. Are willing and able to comply with procedures required in this protocol.
  5. Subjects must not be incarcerated and must be freely willing and able to provide informed consent. Examples of subjects unable to freely provide informed consent may include some adults under legal protection measures (e.g., under guardianship/curatorship) or unable to express their consent and select adults under psychiatric care. Investigator's discretion should be applied.
  6. Diagnosis of moderate to severe active ulcerative colitis with a documented initial response to upadacitinib treatment (defined as adapted Mayo score of 5-9) and subsequent documented loss of response to upadacitinib 30 mg QD dose. This should be within 8 weeks of screening. This will allow for short term non-UC related flares to self-resolve, while at the same time allowing for adequate time interval between appointments.
  7. Subject has documented diagnosis of moderate to severe active UC with a modified Mayo score of 5 to 9 points and endoscopic subscore of 2 to 3 at the time of screening.
  8. Pregnancy testing in females of childbearing potential/individuals of childbearing potential; Contraception Recommendations of this protocol :

    Females of childbearing potential/Individuals of childbearing potential must have a negative serum pregnancy test at the Screening Visit.

  9. Female subjects of childbearing potential must practice at least 1 protocol-specified method of birth control, from Study Day 1 through at least 30 days after the last dose of study drug. Female subjects of nonchildbearing potential do not need to use birth control.

Exclusion Criteria:

  1. Subject with current diagnosis of Crohn's Disease or diagnosis of indeterminate colitis.
  2. Current diagnosis of fulminant colitis and/or toxic megacolon.
  3. History of clinically significant (per investigator's judgment) drug or alcohol abuse within the last 6 months.
  4. Conditions that could interfere with drug absorption including but not limited to short bowel syndrome.
  5. History of colectomy (total or subtotal), ileoanal pouch, Kock pouch, or ileostomy or is planning bowel surgery.
  6. Subject has active TB or latent TB.
  7. Subject who received fecal microbial transplantation within 30 days prior to Baseline.
  8. Subject with new or chronic systemic use of known strong cytochrome P450 (CYP)3A inhibitors or strong CYP3A inducers while on UPA therapy should be evaluated by caring physician as to possibility of this medication being responsible for the loss of response to UPA. Herbal therapies and other traditional medicines are defined as any herbal formulation that is intended to treat or prevent health problems and may include supplements based on herbs which the subject is taking.
  9. Subject currently receiving total parenteral nutrition (TPN) or plan to receive TPN at any time during study treatment.
  10. Subject with positive C. difficile toxin stool assay during screening.
  11. Infection(s) requiring treatment with intravenous anti-infectives within 30 days prior to the Baseline visit or oral/intramuscular anti-infectives within 14 days prior to the baseline visit.
  12. Chronic recurring infection and/or active viral infection that, based on the investigator's clinical assessment, makes the subject an unsuitable candidate for the study
  13. Subject has current or past history of recurrent or disseminated (even a single episode) herpes zoster
  14. Subject has current or past history of disseminated (even a single episode) herpes simplex
  15. Prior or current gastrointestinal (GI) dysplasia, other than completely removed dysplastic lesion in any biopsy performed during or before the screening endoscopy.
  16. History of any malignancy, except for successfully treated nonmelanoma skin cancer (NMSC) or localized carcinoma in situ of the cervix.
  17. History of gastrointestinal (GI) perforation (other than due to appendicitis or mechanical injury), diverticulitis, or significantly increased risk of GI perforation per investigator's judgment.
  18. History of an allergic reaction or significant sensitivity to constituents of upadacitinib (and its excipients)
  19. Subject who previously received stem cell transplantation
  20. Subject has been a previous recipient of an organ transplant which requires continued immunosuppression.
  21. History of cerebrovascular accident, myocardial infarction, coronary stenting, or aortocoronary bypass stenting or retinal vein occlusion; however, if the investigator determines there are no suitable treatment alternatives available for a subject who has experienced one of these events more than 6 months prior to the Baseline visit, the investigator must document a favorable benefit-risk assessment to justify the subject's inclusion in the study.

    In patients with known VTE risk factors other than cardiovascular or alignancy risk factors, participation in this clinical trial is considered the most suitable treatment option among treatment alternatives and the risks and benefits have been discussed with the subject.

  22. A serious AE or AE that is identified or a possible risk of UPA during prior treatment with upadacitinib that is deemed to have a causal relationship with upadacitinib by Investigator
  23. Subjects who have been treated with any investigational drug of chemical or biologic nature within 30 days or five half-lives (whichever is longer) prior to the first dose of study treatment or who are currently enrolled in another interventional clinical study.
  24. Received treatment with rectal aminosalicylates or corticosteroids, other enemas/suppositories (other than required for endoscopy), within 7 days prior to the Screening endoscopy and during the remainder of the Screening Period.
  25. Received cyclosporine, tacrolimus, mycophenolate mofetil or thalidomide within 30 days prior to Baseline.
  26. Subjects who received azathioprine or 6-mercaptopurine within 10 days of Baseline.
  27. Subjects who received intravenous corticosteroids within 14 days prior to screening or during the screening period.
  28. Subjects who require corticosteroids to remain in the study
  29. Subject who received non-steroidal anti-inflammatory drugs (NSAIDs) (except topicalNSAIDs and the useof low dose aspirin for cardiovascular [CV] protection) within 7 days prior to baseline

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:不适用
  • 介入模型:单组作业
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:Upadacitinib re-induction strategy
Patients with moderate to severe active UC who have had a loss of response to upadacitinib 30 mg maintenance dose will receive receive higher dose of upadacitinib for a specified period. Followed by a 52-week maintenance phase with upadacitinib 30 mg QD.
Upadacitinib is a selective JAK1 inhibitor. In this study, patients receive higher dose of upadacitinib as re-induction strategy. in the first timepoint, patients are managed according to disease response : patients without clinical response continue on higher updacatinib dose , patients with clinical response undergo endoscopy : patients with a positive endoscopy continue higher upadacitinib dose and patients with a negative endoscopy transition to the maintenance dose.

研究衡量的是什么?

主要结果指标

结果测量
大体时间
To determine the rate of re-capture of clinical response in subjects with moderate to severe active ulcerative colitis who had a loss of response to upadacitinib 30 mg QD maintenance dose prior to the study entry.
大体时间:from baseline to Wk8
from baseline to Wk8

次要结果测量

结果测量
大体时间
To determine the proportion of subjects achieving clinical response
大体时间:From baseline to Wk8
From baseline to Wk8
To determine the proportion of subjects achieving clinical response
大体时间:Frome baseline to Wk16
Frome baseline to Wk16
To determine the rate of clinical remission
大体时间:Frome baseline to wk8 and wk16
Frome baseline to wk8 and wk16
To determine the proportion of subjects achieving clinical remission
大体时间:Frome basline to 52-week maintenance period.
Frome basline to 52-week maintenance period.

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Lucine Vuitton、CHU de Besançon, FRANCE

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年11月15日

初级完成 (估计的)

2029年11月1日

研究完成 (估计的)

2030年4月1日

研究注册日期

首次提交

2026年7月8日

首先提交符合 QC 标准的

2026年7月8日

首次发布 (实际的)

2026年7月14日

研究记录更新

最后更新发布 (实际的)

2026年7月31日

上次提交的符合 QC 标准的更新

2026年7月29日

最后验证

2026年7月1日

更多信息

与本研究相关的术语

其他研究编号

  • GETAID-2026-01
  • 2026-526174-16-00 (克蒂斯)

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

未定

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

在美国制造并从美国出口的产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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