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Alagille Syndrome - 13 Studies Found

Status Study
Completed Study Name: An Open Label, Single-dose, Single Period ADME Study of A4250 in Healthy Subjects
Condition: Orphan Cholestatic Liver Diseases Progressive Familial Intrahepatic Cholestasis
Date: 2017-02-27
Interventions: Drug: 3 mg [14C]-A4250 capsule Each subject will receive a single administration of 3 mg [14C]-A4250 cap
Completed Study Name: A Safety and Pharmakokinetic Study of A4250 Alone or in Combination With A3384
Condition: Orphan Cholestatic Liver Diseases Primary Biliary Cirrhosis
Date: 2016-11-01
Interventions: Drug: A4250 Drug: CRC (A3384)
Enrolling by invitation Study Name: FibroScan™ in Pediatric Cholestatic Liver Disease Study Protocol
Condition: Biliary Atresia Alagille Syndrome
Date: 2016-09-20
Interventions: Other: Liver Stiffness Measurement (LSM) LSM will be measured via transient elastography utilizing the n
Active, not recruiting Study Name: A Long-Term, Open-Label Study of LUM001 With a Double-Blind, Placebo Controlled, Randomized Drug Withdrawal Period to Evaluate Safety and Efficacy in Children With Alagille Syndrome
Condition: Alagille Syndrome
Date: 2014-06-09
Interventions: Drug: LUM001 LUM001 administer
Completed Study Name: Validation of the Itch Reported Outcome (ItchRO) Diaries in Pediatric Cholestatic Liver Disease
Condition: Alagille Syndrome Progressive Familial Intrahepatic Cholestasis
Date: 2014-05-01
Active, not recruiting Study Name: 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
Condition: Alagille Syndrome
Date: 2014-04-16
Interventions: Drug: LUM001 Administered orally daily
Completed Study Name: Evaluation of LUM001 in the Reduction of Pruritus in Alagille Syndrome
Condition: Alagille Syndrome
Date: 2014-02-05
Interventions: Drug: LUM001 LUM001 administer
Active, not recruiting Study Name: 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)
Condition: Alagille Syndrome
Date: 2014-01-23
Interventions: Drug: LUM001 Dosing of LUM001 with the objective of achieving optimal control of pruritus at a dose leve
Completed Study Name: Safety and Efficacy Study of LUM001 in the Treatment of Cholestatic Liver Disease in Patients With Alagille Syndrome
Condition: Alagille Syndrome
Date: 2013-07-16
Interventions: Drug: LUM001 Drug: Placebo
Recruiting Study Name: Characterization of Pulmonary Artery Stenoses in Alagille Syndrome - a Medical Record Review
Condition: Alagille Syndrome
Date: 2012-01-18
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