- Trials with a EudraCT protocol (335)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
335 result(s) found for: HCC.
Displaying page 5 of 17.
| EudraCT Number: 2020-005504-18 | Sponsor Protocol Number: APHP201185 | Start Date*: 2021-05-21 |
| Sponsor Name:Assistance Publique – Hôpitaux de Paris (AP-HP) | ||
| Full Title: Lenvatinib in neo-adjuvant and adjuvant therapy for poor-prognosis BCLC A HepatoCellular Carcinoma treated by ablative procedure in a curative intent: multicentre phase 2 therapeutic trial | ||
| Medical condition: NA | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-003555-16 | Sponsor Protocol Number: 21469 | Start Date*: 2020-12-11 | |||||||||||
| Sponsor Name:BAYER AG | |||||||||||||
| Full Title: An Open-Label Study of Regorafenib in Combination with Pembrolizumab in Patients with Advanced or Metastatic Hepatocellular Carcinoma (HCC) after PD-1/PD-L1 Immune Checkpoint Inhibitors | |||||||||||||
| Medical condition: A type of liver cancer which may have spread to nearby tissue and is unlikely to be cured or controlled with treatment | |||||||||||||
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| Population Age: | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) DE (Completed) IT (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-002755-29 | Sponsor Protocol Number: CA209-9DX | Start Date*: 2018-11-19 | |||||||||||
| Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
| Full Title: A Phase 3, Randomized, Double-blind Study of Adjuvant Nivolumab versus Placebo for Participants with Hepatocellular Carcinoma Who Are at High Risk of Recurrence after Curative Hepatic Resection or ... | |||||||||||||
| Medical condition: Hepatocellular Carcinoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Trial now transitioned) ES (Ongoing) AT (Trial now transitioned) FR (Trial now transitioned) GB (GB - no longer in EU/EEA) BE (Trial now transitioned) NL (Trial now transitioned) IT (Trial now transitioned) RO (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-000390-67 | Sponsor Protocol Number: ACT15377 | Start Date*: 2020-01-13 | |||||||||||
| Sponsor Name:Sanofi-aventis recherche & développement | |||||||||||||
| Full Title: A Phase 1/2 open-label, multi-center, safety, preliminary efficacy and pharmacokinetic (PK) study of isatuximab (SAR650984) in combination with atezolizumab or isatuximab alone in patients with adv... | |||||||||||||
| Medical condition: Neoplasm | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) BE (Completed) NL (Completed) ES (Ongoing) GR (Prematurely Ended) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-002423-19 | Sponsor Protocol Number: BGB-A317-301 | Start Date*: 2018-08-24 | |||||||||||
| Sponsor Name:BeiGene, Ltd. | |||||||||||||
| Full Title: A Randomized, Open-label, Multicenter Phase 3 Study to Compare the Efficacy and Safety of BGB-A317 versus Sorafenib as First-Line Treatment in Patients with Unresectable Hepatocellular Carcinoma | |||||||||||||
| Medical condition: Unresectable Hepatocellular Carcinoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) DE (Completed) CZ (Completed) FR (Completed) ES (Ongoing) PL (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-003649-14 | Sponsor Protocol Number: Bay73-4506/15982 | Start Date*: 2013-01-30 | |||||||||||
| Sponsor Name:Bayer AG | |||||||||||||
| Full Title: A randomized, double blind, placebo-controlled, multicenter phase III study of regorafenib in patients with hepatocellular carcinoma (HCC) after sorafenib | |||||||||||||
| Medical condition: Hepatocellular carcinoma (HCC) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) BE (Completed) GB (Completed) AT (Completed) ES (Completed) CZ (Completed) FR (Completed) HU (Completed) NL (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-004597-26 | Sponsor Protocol Number: IMMUWIN | Start Date*: 2020-09-15 | ||||||||||||||||
| Sponsor Name:Frankfurter Institut für Klinische Krebsforschung IKF GmbH am Krankenhaus Nordwest | ||||||||||||||||||
| Full Title: A Phase II study of immunotherapy with durvalumab (MEDI4736) and tremelimumab in combination with Y-90 SIRT for intermediate stage HCC - IMMUWIN | ||||||||||||||||||
| Medical condition: Intermediate stage hepatocellular carcinoma (HCC) | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2015-001663-39 | Sponsor Protocol Number: D4190C00022 | Start Date*: 2015-11-27 | |||||||||||
| Sponsor Name:MedImmune | |||||||||||||
| Full Title: A Study of Safety, Tolerability, and Clinical Activity of MEDI4736 and Tremelimumab Administered as Monotherapy and in Combination to Subjects with Unresectable Hepatocellular Carcinoma | |||||||||||||
| Medical condition: Hepatocellular Carcinoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-000051-16 | Sponsor Protocol Number: JX594-HEP018 | Start Date*: 2012-12-21 | |||||||||||
| Sponsor Name:Jennerex, Inc | |||||||||||||
| Full Title: A Phase 2b Randomized Open-Label Trial of JX-594 (Vaccinia GM-CSF / TK-deactivated Virus) Plus Best Supportive Care Versus Best Supportive Care in Patients with Advanced Hepatocellular Carcinoma Wh... | |||||||||||||
| Medical condition: Advanced hepatocellular carcinoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) ES (Completed) IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-002992-33 | Sponsor Protocol Number: E7080-G000-304 | Start Date*: 2013-07-04 | |||||||||||
| Sponsor Name:Eisai Limited | |||||||||||||
| Full Title: A Multicenter, Randomized, Open-Label, Phase 3 Trial to Compare the Efficacy and Safety of Lenvatinib (E7080) Versus Sorafenib in First-Line Treatment of Subjects With Unresectable Hepatocellular... | |||||||||||||
| Medical condition: Unresectable Hepatocellular Carcinoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) DE (Completed) GB (GB - no longer in EU/EEA) ES (Completed) PL (Completed) BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-010760-42 | Sponsor Protocol Number: 4SC-201-1-2009 | Start Date*: 2009-06-19 | |||||||||||
| Sponsor Name:4SC AG | |||||||||||||
| Full Title: A proof-of-concept Phase II study to evaluate efficacy, safety and pharmacokinetics of 4SC-201 and the treatment combination of Sorafenib plus 4SC-201 in patients with hepatocellular carcinoma exhi... | |||||||||||||
| Medical condition: Patients aged ≥ 18, of both gender, with advanced stage hepatocellular carcinoma, BCLC class B (intermediate stage, performance status-ECOG 0, multinodular HCC) or C (advanced stage, performance st... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-002491-14 | Sponsor Protocol Number: WO41535 | Start Date*: 2019-12-17 | |||||||||||
| Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
| Full Title: A PHASE III, MULTICENTER, RANDOMIZED, OPEN-LABEL STUDY OF ATEZOLIZUMAB (ANTI-PD-L1 ANTIBODY) PLUS BEVACIZUMAB VERSUS ACTIVE SURVEILLANCE AS ADJUVANT THERAPY IN PATIENTS WITH HEPATOCELLULAR CARCINOM... | |||||||||||||
| Medical condition: High-risk hepatocellular carcinoma (HCC) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Trial now transitioned) CZ (Trial now transitioned) FR (Trial now transitioned) ES (Ongoing) PL (Trial now transitioned) NL (Trial now transitioned) BE (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-001985-86 | Sponsor Protocol Number: JX594-HEP024 | Start Date*: 2016-09-29 | |||||||||||
| Sponsor Name:SillaJen Inc. | |||||||||||||
| Full Title: A Phase 3 Randomized, Open-Label Study Comparing Pexa-Vec (Vaccinia GM-CSF / Thymidine Kinase-Deactivated Virus) Followed by Sorafenib Versus Sorafenib in Patients with Advanced Hepatocellular Carc... | |||||||||||||
| Medical condition: Advanced Hepatocellular Carcinoma (HCC) without prior systemic therapy | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) PT (Prematurely Ended) PL (Prematurely Ended) FR (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-003691-31 | Sponsor Protocol Number: YO40245 | Start Date*: Information not available in EudraCT | |||||||||||||||||||||||||||||||
| Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||||||||||||||||||||||
| Full Title: A PHASE III, OPEN-LABEL, RANDOMIZED STUDY OF ATEZOLIZUMAB IN COMBINATION WITH BEVACIZUMAB COMPARED WITH SORAFENIB IN PATIENTS WITH UNTREATED LOCALLY ADVANCED OR METASTATIC HEPATOCELLULAR CARCINOMA | |||||||||||||||||||||||||||||||||
| Medical condition: Locally advanced or Metastatic hepatocellular carcinoma (HCC) | |||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
| Trial protocol: PL (Completed) DE (Completed) GB (GB - no longer in EU/EEA) CZ (Completed) ES (Prematurely Ended) IT (Completed) | |||||||||||||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2012-002206-52 | Sponsor Protocol Number: CD-ON-MEDI4736-1108 | Start Date*: 2012-12-05 |
| Sponsor Name:MedImmune | ||
| Full Title: A Phase 1/2 Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of MEDI4736 in Subjects with Advanced Solid Tumors | ||
| Medical condition: Advanced Solid Tumors | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) GB (Completed) DK (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2005-003284-22 | Sponsor Protocol Number: AI463080 | Start Date*: 2007-03-19 | |||||||||||
| Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
| Full Title: Randomized, Observational Study of Entecavir to Assess Long-term Outcomes Associated with Nucleoside/Nucleotide Monotherapy for Patients with Chronic HBV Infection: The REALM Study | |||||||||||||
| Medical condition: CHRONIC HEPATITIS B VIRUS INFECTION | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) DE (Completed) ES (Completed) IT (Completed) PT (Completed) GR (Completed) CZ (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-003354-24 | Sponsor Protocol Number: XL184–312 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:Exelixis, Inc. | |||||||||||||
| Full Title: A Randomized, Controlled Phase 3 Study of Cabozantinib (XL184) in Combination with Atezolizumab versus Sorafenib in Subjects with Advanced Hepatocellular Carcinoma Who Have Not Received Previous... | |||||||||||||
| Medical condition: Hepatocellular carcinoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) HU (Trial now transitioned) NL (Completed) ES (Ongoing) BE (Trial now transitioned) DE (Completed) AT (Completed) PL (Completed) FR (Trial now transitioned) GB (GB - no longer in EU/EEA) IT (Completed) RO (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-001049-10 | Sponsor Protocol Number: M14-726 | Start Date*: 2015-09-24 | |||||||||||
| Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
| Full Title: Open-label Study to Evaluate the Safety and Efficacy of the Combination of Ombitasvir, Paritaprevir/r ± Dasabuvir with Ribavirin (RBV) in Adult Patients with GT1 or GT4 Chronic HCV Infection and Re... | |||||||||||||
| Medical condition: Chronic Hepatitis C Infection | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-005422-76 | Sponsor Protocol Number: CRAD001C24100 | Start Date*: 2008-09-01 | |||||||||||
| Sponsor Name:PD Dr. Gerhard Treiber | |||||||||||||
| Full Title: Antiangiogenic Treatment of Advanced or Metastatic Hepatocellular Cancer (HCC) - An open label, stratified, single-arm phase II study of Bevacizumab and RAD001 | |||||||||||||
| Medical condition: Antiangiogenic Treatment of Advanced or Metastatic Hepatocellular Cancer (HCC) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-002929-35 | Sponsor Protocol Number: CFGF401X2101 | Start Date*: 2015-01-02 | ||||||||||||||||
| Sponsor Name:Novartis Farmacéutica, S.A. | ||||||||||||||||||
| Full Title: A phase I/II, multicenter, open-label study of oral FGF401 in adult patients with hepatocellular carcinoma or solid malignancies characterized by positive FGFR4 and KLB expression | ||||||||||||||||||
| Medical condition: Hepatocellular carcinoma or other solid tumors characterized by positive FGFR4 and KLB expression | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: ES (Completed) DE (Prematurely Ended) FR (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
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