- Trials with a EudraCT protocol (20)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
20 result(s) found for: Secondary sclerosing cholangitis.
Displaying page 1 of 1.
EudraCT Number: 2018-004258-77 | Sponsor Protocol Number: CM-101-PSC-001 | Start Date*: 2019-02-05 | |||||||||||
Sponsor Name:ChemomAb Ltd. | |||||||||||||
Full Title: A Phase 2, Open Label, Multiple Center Study to Evaluate the Safety, Tolerability, and Efficacy of CM-101 Administered for 12 Weeks in Adult Subjects with Primary Sclerosing Cholangitis. | |||||||||||||
Medical condition: Treatment of Primary Sclerosing Cholangitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-002754-31 | Sponsor Protocol Number: NUC-3/PSC | Start Date*: 2012-08-02 | |||||||||||
Sponsor Name:Dr. Falk Pharma GmbH | |||||||||||||
Full Title: Double-blind, randomized, placebo-controlled, phase II dose-finding study comparing different doses of norursodeoxycholic acid capsules with placebo in the treatment of primary sclerosing cholangitis | |||||||||||||
Medical condition: primary sclerosing cholangitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) NL (Completed) LT (Completed) NO (Completed) SE (Completed) GB (Completed) ES (Completed) FI (Completed) HU (Completed) DK (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003392-30 | Sponsor Protocol Number: 15-0106 | Start Date*: 2016-04-18 | |||||||||||||||||||||||||||||||
Sponsor Name:NGM Biopharmaceuticals, Inc. | |||||||||||||||||||||||||||||||||
Full Title: A PHASE 2, RANDOMIZED, DOUBLE BLIND, PLACEBO CONTROLLED, PARALLEL GROUP, MULTIPLE CENTER STUDY TO EVALUATE THE SAFETY, TOLERABILITY, AND EFFICACY OF NGM282 ADMINISTERED FOR 12 WEEKS IN PATIENTS WIT... | |||||||||||||||||||||||||||||||||
Medical condition: PRIMARY SCLEROSING CHOLANGITIS (PSC) | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: GB (Completed) NL (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-002945-39 | Sponsor Protocol Number: CM-101-PSC-101 | Start Date*: 2020-04-15 | |||||||||||
Sponsor Name:ChemomAb Ltd | |||||||||||||
Full Title: A Phase 2a, Randomized, Double-Blind, Placebo-Controlled, Clinical Trial Evaluating the Safety and Efficacy of CM-101 in Subjects with Primary Sclerosing Cholangitis | |||||||||||||
Medical condition: Primary Sclerosing Cholangitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-003367-19 | Sponsor Protocol Number: NUC-5/PSC | Start Date*: 2017-09-28 | |||||||||||
Sponsor Name:Dr. Falk Pharma GmbH | |||||||||||||
Full Title: Double-blind, randomized, placebo-controlled, phase III study comparing norursodeoxycholic acid capsules with placebo in the treatment of primary sclerosing cholangitis | |||||||||||||
Medical condition: Primary Sclerosing Cholangitis (PSC) is a slowly progressing chronic cholestatic liver disease of assumed autoimmune, but finally unidentified etiology, characterized by a chronic inflammatory and ... | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) AT (Trial now transitioned) GB (GB - no longer in EU/EEA) HU (Trial now transitioned) LT (Completed) FI (Trial now transitioned) CZ (Prematurely Ended) BE (Completed) DK (Trial now transitioned) NL (Trial now transitioned) FR (Trial now transitioned) SE (Completed) NO (Trial now transitioned) PL (Trial now transitioned) IE (Prematurely Ended) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-002393-37 | Sponsor Protocol Number: RG_13-027 | Start Date*: 2015-01-06 | |||||||||||
Sponsor Name:University of Birmingham | |||||||||||||
Full Title: A single arm, two-stage, multi-centre, phase II clinical trial investigating the safety and activity of the use of BTT1023, a human monoclonal antibody targeting vascular adhesion protein (VAP-1), ... | |||||||||||||
Medical condition: Primary Sclerosing Cholangitis (PSC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-000875-37 | Sponsor Protocol Number: VanC-IT | Start Date*: 2022-11-03 | |||||||||||
Sponsor Name:UNIVERSITÀ DEGLI STUDI MILANO BICOCCA | |||||||||||||
Full Title: A Prospective, Randomized, Placebo-controlled Clinical Trial of oral vancomycin in adults and young adults (15-17 years old) affected by Primary Sclerosing Cholangitis with or without Inflammatory ... | |||||||||||||
Medical condition: Primary Sclerosing Cholangitis | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-000204-14 | Sponsor Protocol Number: GS-US-428-4194 | Start Date*: 2019-09-11 | |||||||||||
Sponsor Name:Gilead Sciences, Inc. | |||||||||||||
Full Title: A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study Evaluating the Safety, Tolerability, and Efficacy of Cilofexor in Non-Cirrhotic Subjects with Primary Sclerosing Cholangitis | |||||||||||||
Medical condition: Primary Sclerosing Cholangitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Prematurely Ended) BE (Completed) AT (Completed) GB (GB - no longer in EU/EEA) DK (Prematurely Ended) FR (Completed) ES (Restarted) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002473-61 | Sponsor Protocol Number: GS-US-321-0102 | Start Date*: 2013-05-08 | |||||||||||
Sponsor Name:Gilead Sciences Inc | |||||||||||||
Full Title: A Phase 2b, Dose-Ranging, Randomized, Double-Blind, Placebo-Controlled Trial Evaluating the Safety and Efficacy of GS-6624, a Monoclonal Antibody Against Lysyl Oxidase Like 2 (LOXL2) in Subjects wi... | |||||||||||||
Medical condition: Primary Sclerosing Cholangitis (PSC) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) SE (Completed) IT (Completed) DK (Completed) ES (Completed) BE (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-005558-21 | Sponsor Protocol Number: LUM001-401 | Start Date*: 2015-03-25 | |||||||||||
Sponsor Name:Lumena Pharmaceuticals LLC | |||||||||||||
Full Title: A Pilot, Open-Label Study to Evaluate the Safety, Tolerability and Efficacy of LUM001, an Apical Sodium-dependent Bile Acid Transporter Inhibitor (ASBTi), in Patients with Primary Sclerosing Cholan... | |||||||||||||
Medical condition: Primary sclerosing cholangitis (PSC) is a chronic cholestatic liver disease of unknown aetiology. PSC is characterized by inflammation and fibrosis of the intra- and extrahepatic biliary tree re... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-002695-37 | Sponsor Protocol Number: CLIN-60190-453 | Start Date*: 2023-04-27 | |||||||||||
Sponsor Name:Ipsen Bioscience, Inc. | |||||||||||||
Full Title: A Phase II, Multicenter, Double-Blind, Randomised, Placebo-Controlled Study and Open-Label Long Term Extension to Evaluate the Safety and Efficacy of Elafibranor in Adult Participants with Primary ... | |||||||||||||
Medical condition: Adults patients with Primary Sclerosing Cholangitis (PSC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) ES (Ongoing) PT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-002205-38 | Sponsor Protocol Number: 747-207 | Start Date*: 2015-12-02 | |||||||||||
Sponsor Name:INTERCEPT PHARMACEUTICALS INC. | |||||||||||||
Full Title: A Phase 2, Randomized, Double-Blind, Placebo-Controlled,Dose-Finding, Clinical Trial Evaluating the Efficacy and Safety of Obeticholic Acid in Subjects with Primary Sclerosing Cholangitis | |||||||||||||
Medical condition: Primary Sclerosing Cholangitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001438-27 | Sponsor Protocol Number: 48885 | Start Date*: 2015-08-19 |
Sponsor Name:Academic Medical Center | ||
Full Title: The effect of bezafibrate on cholestatic itch | ||
Medical condition: Primary biliary cirrhosis (PBC) Primary sclerosing cholangitis (PSC) Secondary sclerosing cholangitis (SSC) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) ES (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2021-002526-25 | Sponsor Protocol Number: EP-547-201 | Start Date*: 2022-11-30 | |||||||||||
Sponsor Name:Escient Pharmaceuticals, Inc. | |||||||||||||
Full Title: Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Effects of EP547 in Subjects with Cholestatic Pruritus Due to Primary Biliary Cholangitis or Primary Sclerosing Cholangitis | |||||||||||||
Medical condition: Subjects with Cholestatic Pruritus Due to Primary Biliary Cholangitis or Primary Sclerosing Cholangitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001760-30 | Sponsor Protocol Number: CB8025-21845 | Start Date*: 2019-10-11 | |||||||||||
Sponsor Name:CymaBay Therapeutics | |||||||||||||
Full Title: A Phase 2, Randomized, Double-Blind, Placebo-Controlled Multiple Center Study to Evaluate the Safety, Tolerability, and Efficacy of Seladelpar Administered for 24 Weeks in Adult Patients with Prima... | |||||||||||||
Medical condition: Primary Sclerosing Cholangitis (PSC) is a chronic cholestatic liver disease that is characterized by diffuse inflammation and fibrosis of the bile ducts. The intra and/or extrahepatic bile ducts ca... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) PL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001157-32 | Sponsor Protocol Number: A4250-003 | Start Date*: 2015-05-13 |
Sponsor Name:Albireo AB | ||
Full Title: An exploratory Phase II Study to demonstrate the Safety and Efficacy of A4250 in Children with Cholestatic Pruritus | ||
Medical condition: Patients wih Cholestatic Pruritus | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) DK (Completed) DE (Completed) GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-020480-21 | Sponsor Protocol Number: pro-duct001 | Start Date*: 2010-11-18 |
Sponsor Name:Universitätsmedizin Charite | ||
Full Title: Feasibility and efficacy of adjuvant gemcitabine chemotherapy after liver transplantation for proximal bile duct cancer | ||
Medical condition: proximal bile duct cancer | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-002404-18 | Sponsor Protocol Number: NRL972-03/2006 (CIR) | Start Date*: 2008-04-04 | |||||||||||
Sponsor Name:Norgine Limited | |||||||||||||
Full Title: A multi-centre, multi-national open study in patients with hepatic cirrhosis to characterise the association between the pharmacokinetics of NRL972 and disease severity | |||||||||||||
Medical condition: Hepatic cirrhosis. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) LT (Completed) IT (Completed) BG (Completed) AT (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-004695-18 | Sponsor Protocol Number: RES-Q-HR | Start Date*: 2020-12-02 | ||||||||||||||||||||||||||
Sponsor Name:Heinrich-Heine-University Düsseldorf | ||||||||||||||||||||||||||||
Full Title: Reconvalescent plasma/Camostat mesylate early in Sars-CoV-2 Q-PCR positive high risk individuals | ||||||||||||||||||||||||||||
Medical condition: The novel coronavirus designated SARS CoV-2, and the disease caused by this virus designated COVID-19. No treatment is available for early disease stages and non-hospitalized patients to date. This... | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-004730-42 | Sponsor Protocol Number: IQVIA-ODYS-001-LZA45541 | Start Date*: 2022-10-24 | |||||||||||||||||||||||||||||||
Sponsor Name:IQVIA RDS FRANCE SAS | |||||||||||||||||||||||||||||||||
Full Title: Prospective evaluation of potential effects of repeated gadolinium-based contrast agent (GBCA) administrations of the same GBCA on motor and cognitive functions in neurologically normal adults in c... | |||||||||||||||||||||||||||||||||
Medical condition: Long term potential effect of repeated exposure to either a linear or a macrocyclic gadolinium-based contrast agent (GBCA) on change from baseline to Year 5 in motor and cognitive function among ne... | |||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: NL (Completed) IT (Trial now transitioned) FR (Trial now transitioned) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
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