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临床试验/NCT04483531
NCT04483531No Longer Available不适用

Odevixibat (A4250) for the Treatment of Progressive Familial Intrahepatic Cholestasis (Expanded Access Program)

Albireo1 个研究点 分布在 1 个国家开始时间: 2020年7月23日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
No Longer Available
发起方
Albireo
试验地点
1

研究概览

简要总结

To provide treatment access to patients with PFIC in the US who have pruritus and elevated serum bile acids and who are not able to enroll in A4250-008 (PEDFIC2) for the following reasons: 1) Do not meet eligibility criteria for PEDFIC 2; 2) Are not able to get to a PEDFIC 2 site for geographical reasons, and 3) Do meet the eligibility criteria for PEDFIC 2 after recruitment has been completed

详细描述

Eligible patients will be enrolled into this expanded-access program and treated with an oral dose of 120 μg/kg/day of odevixibat and evaluated on an ongoing basis.

研究设计

研究类型
Expanded Access

入排标准

性别
All
接受健康志愿者
否

入选标准

  • •A male or female patient of any age, with a clinical diagnosis of PFIC, and with a body weight ≥5 kg at Screening visit
  • •Patient must have a clinical diagnosis of PFIC
  • •Patient must have clinically confirmed pruritus
  • •Patient must have elevated serum bile acid levels, specifically measured to be ≥2 × the upper limit of normal (ULN) prior to start of medication
  • •Patient and/or legal guardian must sign informed consent (and assent) as appropriate. Patients who turn 18 years of age (or legal age per country) during

排除标准

  • •Patient is expected to have a liver transplant within 6 months of Screening
  • •Decompensated liver disease, coagulopathy, history or presence of clinically significant ascites, variceal hemorrhage, and/or encephalopathy
  • •International normalized ratio (INR) >1.4 (the patient may be treated with Vitamin K intravenously, and if INR is ≤1.4 at resampling the patient may be started on program medication)
  • •Serum ALT >10 × ULN at Screening
  • •Serum ALT >15 × ULN at any time point during the last 6 months unless an alternate etiology was confirmed for the elevation
  • •Total bilirubin >10 × ULN at Screening
  • •Any patient who is pregnant, lactating, or planning to get pregnant
  • •Patients who qualify for enrollment in other Phase 2 or Phase 3 trials intended to support marketing approval in PFIC

研究者

发起方
Albireo
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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