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临床试验/NCT02425865
NCT02425865已完成4 期

Intensive Treatment to Reach the Target With Golimumab in ulcErative coliTis- In-TARGET

Groupe d'Etude Therapeutique des Affections Inflammatoires Digestives23 个研究点 分布在 2 个国家目标入组 202 人开始时间: 2016年12月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
202
试验地点
23
主要终点
Continuous Clinical Response and Endoscopic Remission

研究概览

简要总结

PHASE: IV

TYPE OF STUDY: With direct benefit

DESCRIPTIVE: multicenter, open-label, uncontrolled trial

INCLUSION CRITERIA: Adults with moderate to severe ulcerative colitis who failed corticosteroids and immunosupressive therapy, or are intolerant to immunosuppressors. All included patients will be naïve to anti-TNF therapy. Active disease at golimumab treatment initiation defined as a MAYO score ≥6 and with an endoscopic sub score ≥2.

OBJECTIVE: To determine the proportion of patients with Continuous Clinical Response (CCR) and endoscopic remission after one year of golumimab at week 54.

STUDY DESIGN:

Induction Phase :

Week 0: golimumab 200mg- Week 2: golimumab 100 mg- Week 6: golimumab 50 mg

Maintenance Phase I : Week 10-Week 54 Week 10-Week 54 • Patients with primary clinical response*: Standard regimen with golimumab 50 mg Q4W (or 100 mg Q4W if > 80 kg)

  • Patients without primary clinical response at week 10 or with flare between week 10-week 54*: Optimization to 100 mg Q4W (or combination therapy with azathioprine if > 80 kg or switch from azathioprine to methotrexate if already on azathioprine at golimumab initiation or patient with known intolerance to thiopurines)

  • Early escape at Week 18: Primary non-responders who are still not responding at week 18 to dose optimization at Weeks 10 and 14 will be considered treatment failures and will be followed up (call or visit) at week 54 for safety.

  • Clinical response is defined as a decrease from baseline in the Mayo score ≥30% and ≥3 points, accompanied by either a rectal bleeding sub score of 0 or 1 or a decrease from baseline in the rectal bleeding sub score ≥1

Intermittent Phase II : Week 54-Week 108

• Patients with CCR and MH at week 54 and on golimumab 50 mg every 4 weeks: Stop golimumab and continuation of thiopurines or methotrexate if on combination therapy

• Patients with CCR and MH at week 54 and on golimumab 100 mg every 4 weeks: De-escalation to 50 mg every 4 weeks and continuation of thiopurines or methotrexate if on combination therapy

• Restart/Escalate golimumab on flare (defined in section 4 of the protocol) to the phase I dose; 50 mg q4wk or 100mg q4wk (similar to the phase I regimen)

详细描述

NUMBER OF PATIENTS: 200 patients

INCLUSION PERIOD: 33 months

STUDY DURATION: 57 months

MAIN EVALUATION Primary endpoints

• Week 10-54: proportion of patients in CCR and with MH (endoscopic Mayo score of 0 or 1) at week 54

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

open-label, uncontrolled trial

Other

All patients will receive Standard regimen with golimumab 50 mg Q4W, or 100 mg Q4W if > 80 kg

干预措施: GOLIMUMAB (Drug)

结局指标

主要结局

Continuous Clinical Response and Endoscopic Remission

时间窗: Week 54

proportion of patients in CCR and with MH (endoscopic Mayo score of 0 or 1) at week 54

次要结局

  • Continuous Clinical Response and Endoscopic Remission after discontinuation or de- escalation of golimumab(Week 108)
  • Clinical remission at week 54(week 54)
  • Changes in faecal calprotectin levels from baseline at week 54 and 108(week 108)
  • Colectomy between W0 and W54 and 108(week 108)
  • Histological remission at W54 and 108(week 108)
  • MH (endoscopic score MAYO 0-1) at week 54 and 108(week 108)
  • Efficacy of dose optimization in patients who loose response between week 10 and 54(Week 54)
  • PRO2 (Partial Mayo minus PGA) at week 54 and 108(week 108)
  • CCR between study inclusion and week 54 and 108(week 108)
  • Clinical remission at week 108(week 108)
  • Steroid-free clinical remission at week 54 and 108(week 108)
  • UC-related hospitalizations throughout the trial(week 108)
  • Late responders being in Clinical Response from week 18 to week 54 and with MH at week 54 following treatment intensification in Maintenance Phase(week 108)
  • PRO: Fatigue (FACIT), disability (IBD Disability index), QoL (SHS-IBD VAS)(week 108)
  • PK data (golimumab trough levels and antibodies against golimumab)(week 108)

研究者

发起方
Groupe d'Etude Therapeutique des Affections Inflammatoires Digestives
申办方类型
Other
责任方
Sponsor

研究点 (23)

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