NCT03905330已完成3 期
MRX-502: Randomized Double-blind Placebo-controlled Phase 3 Study to Evaluate the Efficacy and Safety of Maralixibat in the Treatment of Subjects With Progressive Familial Intrahepatic Cholestasis (PFIC) - MARCH-PFIC
适应症
干预措施
相关药物
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 93
- 试验地点
- 31
- 主要终点
- Mean Change in the Average Morning ItchRO(Obs) Severity Score in the Primary Cohort
研究概览
简要总结
The purpose of this study is to determine whether the investigational treatment (maralixibat) is safe and effective in pediatric participants with Progressive Familial Intrahepatic Cholestasis (PFIC).
详细描述
This study was conducted at multiple sites in North America, Europe, Asia and South America.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 1 Year 至 17 Years（Child）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Informed consent and assent (as applicable) per Institutional Review Board/Ethics Committee (IRB/EC)
- •Male or female subjects with a body weight ≥5 kg, who are ≥12 months and <18 years of age at time of baseline
- •Cholestasis as manifested by total sBA ≥3× ULN (applies to primary cohort only)
- •An average AM ItchRO(Obs) score ≥1.5 during 4 consecutive weeks of the screening period, leading to the baseline visit (Visit 1)
- •Completion of at least 21 valid* morning ItchRO(Obs) entries during 4 consecutive weeks of the screening period, leading to the baseline visit (Visit 1) (*valid = completed and not answered as "I don't know"; maximum allowed invalid reports = 7, no more than 2 invalid reports during the last 7 days before randomization)
- •Diagnosis of PFIC based on the following:
- •Chronic cholestasis as manifested by persistent (>6 months) pruritus in addition to biochemical abnormalities and/or pathological evidence of progressive liver disease and
- •Primary Cohort: Subjects with genetic testing results consistent with biallelic disease-causing variation in ABCB11 (PFIC2), based on standard of care genotyping
- •Supplemental Cohort: i. Subjects with genetic testing results consistent with biallelic disease-causing variation in ATP8B1 (PFIC1), ABCB4 (PFIC3), or TJP2 (PFIC4), based on standard of care genotyping. ii. Subjects with PFIC phenotype without a known mutation or with another known mutation not described above or with intermittent cholestasis as manifested by fluctuating sBA levels. iii. Subjects with PFIC after internal or external biliary diversion surgery or for whom internal or external biliary diversion surgery was reversed.
- •Male and females of non-childbearing potential. Males and non-pregnant, non-lactating females of childbearing potential who are sexually active must agree to use acceptable methods of contraception during the study and 30 days following the last dose of the study medication. Females of childbearing potential must have a negative pregnancy test
- •Access to email or phone for scheduled remote visits
- •Ability to read and understand the questionnaires (both caregivers and subjects above the age of assent)
- •Access to consistent caregiver(s) during the study
- •Subject and caregiver willingness to comply with all study visits and requirements.
排除标准
- •Predicted complete absence of bile salt excretion pump (BSEP) function based on the type of ABCB11 mutation (PFIC2), as determined by a standard of care genotyping (applies to primary cohort only). Subjects can enter the study in the Supplemental Cohort (under inclusion criteria 6.ii or 6.iii).
- •Recurrent intrahepatic cholestasis, indicated by a history of sBA levels <3x ULN or intermittent pruritus (applies to primary cohort only)
- •Current or recent history (<1 year) of atopic dermatitis or other non-cholestatic diseases associated with pruritus.
- •History of surgical disruption of the enterohepatic circulation (applies to primary cohort only)
- •Chronic diarrhea requiring intravenous fluid or nutritional intervention for the diarrhea and/or its sequelae at screening or during the 6 months prior to screening
- •Previous or need for imminent liver transplant
- •Decompensated cirrhosis (international normalized ratio [INR] >1.5, albumin <30 g/L, history or presence of clinically significant ascites, variceal hemorrhage, and/or encephalopathy)
- •ALT or total serum bilirubin (TSB) >15× ULN at screening
- •Presence of other liver disease
- •Presence of any other disease or condition known to interfere with the absorption, distribution, metabolism or excretion of drugs, including bile salt metabolism in the intestine (e.g., inflammatory bowel disease), per Investigator discretion
- •Possibly malignant liver mass on imaging, including screening ultrasound
- •Known diagnosis of human immunodeficiency virus (HIV) infection
- •Any prior cancer diagnosis (except for in situ carcinoma) within 5 years of the screening visit (Visit 0)
- •Any known history of alcohol or substance abuse
- •Administration of bile acids or lipid binding resins, or phenylbutyrates during the screening period
- •Criterion has been deleted as of Amendment 3
- •Administration of any investigational drug, biologic, or medical device during the screening period
- •Previous use of an ileal bile acid transporter inhibitor (IBATi)
- •History of non-adherence to medical regimens, unreliability, medical condition, mental instability or cognitive impairment that, in the opinion of the Investigator or Sponsor medical monitor, could compromise the validity of informed consent, compromise the safety of the subject, or lead to nonadherence with the study protocol or inability to conduct the study procedures
- •Known hypersensitivity to maralixibat or any of its excipients.
研究组 & 干预措施
Maralixibat
Experimental
Participants will receive Maralixibat oral solution (up to 600 microgram per kilogram [mcg/kg]) orally twice daily for 26 weeks.
干预措施: Maralixibat (Drug)
Placebo
Placebo Comparator
Participants will receive placebo matched to maralixibat oral solution twice daily for 26 weeks.
干预措施: Placebo (Other)
结局指标
主要结局
Mean Change in the Average Morning ItchRO(Obs) Severity Score in the Primary Cohort
时间窗: MMRM model was used with inputs of the average changes from baseline (BL) to Weeks 1-6, 7-10, 11-14, 15-18, 19-22, 23-26, and other covariates. The average change from BL over Weeks 15-26 is calculated in the model and presented as a single number.
The primary efficacy endpoint is the mean change in the average morning ItchRO(Obs) severity score between baseline and Weeks 15-26, using 4-week average morning ItchRO(Obs) severity scores (Mixed Model Repeated Measures). The baseline average morning ItchRO(Obs) severity score is defined as the 4-week average morning ItchRO(Obs) severity score prior to the first dose of the study medication. ItchRo(Obs) Severity Score = Itch Reported Outcome Observer assessment severity score; scale between 0 (not itchy at all) and 4 (extremely itchy); the lower the score the better.
次要结局
- Mean Change in Total sBA Level in the Primary Cohort.(Baseline and average of Weeks 18, 22 and 26)
- Mean Change in the Average Morning ItchRO(Obs) Severity Score in Participants With PFIC (PFIC1, Nt-PFIC2, PFIC3, PFIC4 and PFIC6)(Between Baseline and Week 15 through Week 26)
- Mean Change in Total sBA Level in Participants With PFIC (PFIC1, PFIC2, PFIC3, PFIC4 and PFIC6)(Between Baseline and average of Weeks 18, 22 and 26)
- Proportion of ItchRO(Obs) Responders in the Primary Cohort(Week 15 to Week 26 using the average value from the three 4-week periods (Weeks 15-18, 19-22 and 23-26))
- Proportion of sBA Responders in the Primary Cohort(Average value from Weeks 18, 22 and 26)
- Proportion of ItchRO(Obs) Responders PFIC (PFIC1, PFIC2, PFIC3, PFIC4 and PFIC6)(From Week 15 to Week 26)
- Proportion of sBA Responders PFIC (PFIC1, PFIC2, PFIC3, PFIC4 and PFIC6)(Week 18 to Week 26)
研究者
研究点 (31)
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