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临床试验/CTRI/2023/05/053075
CTRI/2023/05/053075招募中3 期

A randomized, double-blind, multicenter phase III study to evaluate the long-term efficacy and safety of ABX464 25 mg or 50 mg once daily as a maintenance therapy in subjects with moderately to severely active ulcerative colitis. – ABTECT Maintenance - ABTECT Maintenance

Abivax SA0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
招募中
发起方
Abivax SA

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • A subject will be eligible to participate in this study if ALL the following criteria are met:
  • 1. Subjects must have completed the induction treatment study (ABX464-105 or ABX464-106), and subjects’ clinical response status must be available.
  • 2. Subjects with a valid endoscopy performed at the end of the induction study and results from central reader available at Day 1.
  • 3. Subjects must understand, sign and date the written voluntary informed consent form at the visit prior to any protocol-specific procedures. For under-aged subjects, national requirements regarding consent should also be met.
  • 4. Women of childbearing potential (WOCBP) subjects and male subjects with WOCBP partner must agree to use highly effective contraception methods as stated in Section 4.4. (Contraception) of this protocol.
  • 5. Subjects must be able and willing to comply with study visits and procedures as per protocol.
  • 6. Subjects should be affiliated to a health insurance policy whenever required by a participating country or state.

排除标准

  • Subjects who meet ANY of the following exclusion criteria will be excluded from the study:
  • 1.Subjects who permanently discontinued the study treatment during the induction study (either ABX464-105 or ABX464-106).
  • 2.Subjects who plan to participate in other investigational studies during the maintenance study.
  • 3.Pregnant or breast-feeding women or male subject of a pregnant partner.
  • 4.Male or female subjects planning a pregnancy within the coming 12 months.
  • 5.Subjects who have not adhered to abstinence of prohibited and/or concomitant medications.
  • 6.Any changes in the laboratory values during the induction period that correspond with the following:
  • Hemoglobin = 8.0 g dL-1
  • Absolute neutrophil count < 750 mm-3
  • Platelets < 100,000 mm-3
  • Creatinine clearance < 60 mL.min-1 (Cockcroft-Gault formula)
  • Total serum bilirubin > 1.5 x ULN
  • Alkaline phosphatase, aspartate aminotransferase (AST) and alanine aminotransferase (ALT) > 2 x

研究者

发起方
Abivax SA

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