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
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
相似试验
招募中
1 期
ABTECT-Maintenance – ABX464 Treatment Evaluation for ulcerative Colitis TherapyModerately to severely active ulcerative colitisMedDRA version: 20.0Level: PTClassification code: 10009900Term: Colitis ulcerative Class: 100000004856CTIS2022-500537-84-01Abivax1,241
招募中
3 期
ABTECT - MaintenanceJPRN-jRCT2031230257jRCT Inquiries IQVIA Contact person80
进行中(未招募)
1 期
ABTECT-Maintenance – ABX464 Treatment Evaluation for ulcerative Colitis TherapyCTIS2022-500537-84-00Abivax1,036
进行中(未招募)
不适用
A randomized, double-blind, multi-center phase III study comparing everolimus (RAD001) plus best supportive care versus placebo plus best supportive care in patients with advanced gastric cancer after progression on prior systemic chemotherapyadvanced gastric cancerMedDRA version: 9.1Level: PTClassification code 10017758Term: Gastric cancerEUCTR2008-006544-20-DEovartis Pharma Services AG633
进行中(未招募)
不适用
A randomized, double-blind, multi-center phase III study comparing everolimus (RAD001) plus best supportive care versus placebo plus best supportive care in patients with advanced gastric cancer after progression on prior systemic chemotherapyEUCTR2008-006544-20-NLovartis Pharma Services AG633
