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Alagille Syndrome clinical trials

View clinical trials related to Alagille Syndrome.

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NCT ID: NCT04674761 Completed - Alagille Syndrome Clinical Trials

Efficacy and Safety of Odevixibat in Patients With Alagille Syndrome

ASSERT
Start date: March 19, 2021
Phase: Phase 3
Study type: Interventional

Double-blind, randomized, placebo-controlled, Phase 3 study to investigate the efficacy and safety of odevixibat compared to placebo in Patients with Alagille Syndrome.

NCT ID: NCT03082937 Completed - Clinical trials for Primary Biliary Cirrhosis

An Open Label, Single-dose, Single Period ADME Study of A4250 in Healthy Subjects

Start date: January 31, 2017
Phase: Phase 1
Study type: Interventional

The primary objectives of the study are to assess the mass balance recovery after a single dose of carbon-14 [14C]-A4250 as a capsule and to provide plasma, urine and faecal samples for metabolite profiling and structural identification in healthy male subjects.

NCT ID: NCT02963077 Completed - Clinical trials for Primary Biliary Cirrhosis

A Safety and Pharmakokinetic Study of A4250 Alone or in Combination With A3384

Start date: July 2013
Phase: Phase 1
Study type: Interventional

The primary objectives of the study are to evaluate the safety, tolerability and pharmacokinetics of A4250 after single or multiple oral doses in healthy subjects. In addition, will evaluate A4250 in combination with cholestyramine.

NCT ID: NCT02160782 Completed - Alagille Syndrome Clinical Trials

Safety and Efficacy Study of LUM001 (Maralixibat) With a Drug Withdrawal Period in Participants With Alagille Syndrome (ALGS)

ICONIC
Start date: October 28, 2014
Phase: Phase 2
Study type: Interventional

This is a long-term, open-label study with a double-blind, placebo-controlled, randomized drug withdrawal period in children with Alagille Syndrome (ALGS) designed to evaluate the safety and efficacy of LUM001 (Also known as maralixibat or MRX).

NCT ID: NCT02131623 Completed - Alagille Syndrome Clinical Trials

Validation of the Itch Reported Outcome (ItchRO) Diaries in Pediatric Cholestatic Liver Disease

Start date: July 2014
Phase:
Study type: Observational

The purpose of the study is to validate the ItchRO instrument (a clinical outcome assessment measure of itching) prior to the analysis of longitudinal treatment effect data being generated in ongoing clinical trials.

NCT ID: NCT02117713 Completed - Alagille Syndrome Clinical Trials

An Extension Study to Evaluate the Long-Term Safety and Durability of Effect of LUM001 in the Treatment of Cholestatic Liver Disease in Pediatric Subjects With Alagille Syndrome

IMAGINE-II
Start date: March 16, 2015
Phase: Phase 2
Study type: Interventional

This is a multicentre, extension study of LUM001 in children diagnosed with Alagille Syndrome who have completed participation in a core LUM001 treatment protocol. The primary objective is to evaluate long-term safety and tolerability of LUM001. Efficacy will be assessed by evaluating the effect of LUM001 on the biochemical markers and pruritus associated with Alagille Syndrome.

NCT ID: NCT02057692 Completed - Alagille Syndrome Clinical Trials

Evaluation of LUM001 in the Reduction of Pruritus in Alagille Syndrome

ITCH
Start date: November 24, 2014
Phase: Phase 2
Study type: Interventional

The study is a randomized, double-blind, placebo-controlled study in children with Alagille Syndrome (ALGS). The study will investigate the effects of LUM001, compared to placebo, on pruritus, serum bile acids, liver enzymes, and other biochemical markers in patients with ALGS.

NCT ID: NCT02047318 Completed - Alagille Syndrome Clinical Trials

An Extension Study to Evaluate the Long-Term Safety and Durability of Effect of LUM001 in the Treatment of Cholestatic Liver Disease in Subjects With Alagille Syndrome (ALGS)

IMAGINE
Start date: December 20, 2013
Phase: Phase 2
Study type: Interventional

The purpose of this extension study is to determine the long-term safety and tolerability of an investigational treatment (LUM001 also known as Maralixibat) in children with ALGS who have completed participation in a core LUM001 treatment protocol. Efficacy will be assessed by evaluating the effect of LUM001 on pruritus, biochemical markers of pruritus, as well as biochemical markers of cholestasis and liver disease.

NCT ID: NCT01903460 Completed - Alagille Syndrome Clinical Trials

Safety and Efficacy Study of LUM001 in the Treatment of Cholestatic Liver Disease in Patients With Alagille Syndrome

IMAGO
Start date: August 2013
Phase: Phase 2
Study type: Interventional

The study is a randomized, double-blind, placebo-controlled study to evaluate the safety and tolerability of LUM001. Efficacy will be assessed by evaluating the effect of LUM001 versus placebo on the biochemical markers and pruritus associated with Alagille Syndrome.

NCT ID: NCT01515631 Completed - Alagille Syndrome Clinical Trials

Characterization of Pulmonary Artery Stenoses in Alagille Syndrome - a Medical Record Review

Start date: April 2007
Phase:
Study type: Observational

Patients who have Alagille Syndrome (AGS) also frequently have blockages (or "stenoses") of their pulmonary arteries. Little is known about the degree or variability of these stenoses, or the effect of this disease on the right ventricle (the chamber of the heart which pumps blood to the lungs). This study will first quantify and describe pulmonary artery stenosis in patients with Alagille Syndrome. The study will also assess the effect of these stenoses on the right ventricle. The investigators hope to learn the degree and characteristics of pulmonary artery stenosis in Alagille Syndrome. The investigators also hope to learn the effect of this pulmonary artery stenosis on the right ventricle in patients with Alagille Syndrome. This information is critical in the management of patients with Alagille syndrome, as there is currently no data to guide clinicians on the management of pulmonary artery stenosis. Furthermore, the information from this study may help physicians manage pulmonary artery stenosis in other patients as well.