- Trials with a EudraCT protocol (25)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (5)
25 result(s) found for: Fibrolamellar.
Displaying page 1 of 2.
EudraCT Number: 2005-000427-42 | Sponsor Protocol Number: LT 2005 XX | Start Date*: 2005-04-15 |
Sponsor Name:UK Children’s Cancer Study Group | ||
Full Title: SIOPEL 5 (HCC-1) trial on the hepatocellular carcinoma family of tumours in children/adolescents and young adults | ||
Medical condition: Hepatocellular carcinoma | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-000525-30 | Sponsor Protocol Number: A6181055 | Start Date*: 2006-06-14 | |||||||||||
Sponsor Name:Pfizer Hellas A.E. | |||||||||||||
Full Title: AN OPEN LABEL INTERNATIONAL MULTI-CENTER PHASE 2 ACTIVITY AND SAFETY STUDY OF SU011248 IN PATIENTS WITH UNRESECTABLE HEPATOCELLULAR CARCINOMA | |||||||||||||
Medical condition: Histologically confirmed diagnosis of hepatocellular carcinoma. Patients with the fibrolamellar histology or a mixed histology are not eligible. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-007629-32 | Sponsor Protocol Number: TAC101-202 | Start Date*: 2009-02-19 | |||||||||||
Sponsor Name:Taiho Pharma USA, Inc. | |||||||||||||
Full Title: A PHASE 2, DOUBLE-BLIND, PLACEBO-CONTROLLED, RANDOMIZED, INTERNATIONAL, MULTICENTER STUDY OF ORAL TAC 101 AS SECOND LINE TREATMENT IN PATIENTS WITH ADVANCED HEPATOCELLULAR CARCINOMA WHO RECEIVED SO... | |||||||||||||
Medical condition: Advanced Hepatocellular carcinoma (HCC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) FR (Completed) BE (Completed) IT (Prematurely Ended) DE (Prematurely Ended) GR (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-004800-20 | Sponsor Protocol Number: MK-3475-937 | Start Date*: 2019-08-22 | |||||||||||
Sponsor Name:Merck Sharp & Dohme LLC., a subsidiary of Merck & Co., Inc. | |||||||||||||
Full Title: A Phase 3 Double-blinded, Two-arm Study to Evaluate the Safety and Efficacy of Pembrolizumab (MK-3475) versus Placebo as Adjuvant Therapy in Participants with Hepatocellular Carcinoma and Complete ... | |||||||||||||
Medical condition: Adjuvant treatment of HCC | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Trial now transitioned) SE (Trial now transitioned) DE (Trial now transitioned) NO (Trial now transitioned) HU (Trial now transitioned) PL (Trial now transitioned) BE (Trial now transitioned) DK (Trial now transitioned) FR (Trial now transitioned) ES (Ongoing) GB (GB - no longer in EU/EEA) IT (Trial now transitioned) BG (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-003574-84 | Sponsor Protocol Number: NP27884 | Start Date*: 2012-01-31 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd. | |||||||||||||
Full Title: A Randomized, Placebo-controlled, Double-blind, Multicenter Phase II Trial of Intravenous GC33 at 1600 mg Q2W in Previously Treated Patients with Unresectable Advanced or Metastatic Hepatocellul... | |||||||||||||
Medical condition: Second-line treatment for adult patient with unresectable advanced or metastatic hepatocellular cancer. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) GB (Completed) ES (Completed) DE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000995-14 | Sponsor Protocol Number: MIV-818-101/201 | Start Date*: 2018-08-10 | |||||||||||||||||||||
Sponsor Name:Medivir AB | |||||||||||||||||||||||
Full Title: A Phase 1/2a Study in 3 Parts (Phase 1a and Phase 1b - Dose Escalations and Phase 2a Expansion Cohorts) to Evaluate the Safety, Tolerability, Pharmacokinetics, and Preliminary Antitumor Activity of... | |||||||||||||||||||||||
Medical condition: hepatocellular carcinoma (HCC), intrahepatic cholangiocarcinoma (iCCA), or, metastatic liver disease | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) BE (Completed) ES (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-019318-26 | Sponsor Protocol Number: IMCL_CP12-0919_(I4T-IE-JVBF) | Start Date*: 2010-09-27 | |||||||||||
Sponsor Name:ImClone LLC | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Phase 3 Study of Ramucirumab (IMC-1121B) Drug Product and Best Supportive Care (BSC) Versus Placebo and BSC as Second-Line Treatment in Patients With Hepato... | |||||||||||||
Medical condition: Hepatocellular Carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) DE (Completed) CZ (Completed) PT (Completed) BE (Completed) ES (Completed) AT (Completed) FR (Completed) BG (Completed) HU (Completed) IT (Completed) SE (Completed) NO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-018058-44 | Sponsor Protocol Number: D09-1 | Start Date*: 2010-05-07 | |||||||||||
Sponsor Name:GERCOR | |||||||||||||
Full Title: Proof-of-concept phase II study to evaluate the anti-tumoractivity of sorafenib along with pathological and molecularchanges in tumor samples from patients with resectable hepatocellular carcinoma. | |||||||||||||
Medical condition: Hepatocellular carcinoma resectable | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000591-42 | Sponsor Protocol Number: JX594-IV-HEP021 | Start Date*: 2012-09-21 | |||||||||||
Sponsor Name:Jennerex, Inc | |||||||||||||
Full Title: A Single-Arm, Open-Label Phase 2 Study of JX 594 (Thymidine Kinase-Deactivated Vaccinia Virus plus GM-CSF) Administered by Weekly Intravenous (IV) Infusions in Sorafenib-naïve Patients with Advance... | |||||||||||||
Medical condition: Advanced Hepatocellular Carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000085-32 | Sponsor Protocol Number: TG6006.01 | Start Date*: 2018-05-04 | |||||||||||
Sponsor Name:TRANSGENE SA | |||||||||||||
Full Title: A phase I/IIa trial to evaluate the safety and efficacy of the combination of the oncolytic immunotherapy Pexa-Vec with the PD-1 receptor blocking antibody nivolumab in the first-line treatment of ... | |||||||||||||
Medical condition: Hepatocellular carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000232-34 | Sponsor Protocol Number: NASIR-HCC | Start Date*: 2017-09-11 | |||||||||||
Sponsor Name:Clínica Universidad de Navarra/Universidad de Navarra | |||||||||||||
Full Title: A multicenter, open-label, single-arm study of the safety and antitumoral efficacy of nivolumab in combination with selective internal radiation therapy (SIRT) using SIR-Spheres for the treatment o... | |||||||||||||
Medical condition: Hepatocellular carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-002767-98 | Sponsor Protocol Number: UCDCRC/19/01 | Start Date*: 2020-05-28 | |||||||||||
Sponsor Name:University College Dublin | |||||||||||||
Full Title: A Pilot Study of Combined Immune Checkpoint Inhibition in combination with ablative therapies in Subjects with Hepatocellular Carcinoma (HCC) | |||||||||||||
Medical condition: Patients with Hepatocellular Carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-002625-35 | Sponsor Protocol Number: CALGB80802 | Start Date*: 2013-09-23 |
Sponsor Name:All Ireland Co-operative Oncology Research Group (ICORG) | ||
Full Title: Phase III Randomized Study Of Sorafenib Plus Doxorubicin Versus Sorafenib In Patients With Advanced Hepatocellular Carcinoma (HCC) | ||
Medical condition: Advanced or Metastatic Hepatocellular Carcinoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2015-004567-36 | Sponsor Protocol Number: MK-3475-240 | Start Date*: 2016-05-13 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||
Full Title: A Phase III Study of Pembrolizumab (MK-3475) vs. Best Supportive Care as Second-Line Therapy in Subjects with Previously Systemically Treated Advanced Hepatocellular Carcinoma (KEYNOTE-240) | |||||||||||||
Medical condition: Hepatocellular Carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) DE (Completed) DK (Completed) HU (Completed) FR (Completed) GB (GB - no longer in EU/EEA) PL (Completed) BE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-000707-20 | Sponsor Protocol Number: AFM24-102 | Start Date*: 2021-09-07 | |||||||||||
Sponsor Name:Affimed GmbH | |||||||||||||
Full Title: A Phase 1/2a Open Label, Multicenter Study to Assess the Safety, Tolerability, Pharmacokinetics, and Efficacy of AFM24 in Combination with Atezolizumab in Patients with Selected Advanced/Metastatic... | |||||||||||||
Medical condition: Advanced/Metastatic EGFR-expressing Cancers | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) PL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-002326-75 | Sponsor Protocol Number: 8-55-58102-004 | Start Date*: 2012-09-27 |
Sponsor Name:Ipsen Pharma | ||
Full Title: A multicentre, open label, early stopping design, proof of concept study with tasquinimod in treating patients with advanced or metastatic hepatocellular, ovarian, renal cell and gastric carcinomas. | ||
Medical condition: advanced or metastatic hepatocellular, ovarian, renal cell and gastric carcinomas in patients who have progressed after standard therapies | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) BE (Completed) ES (Completed) | ||
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: 2018-002983-26 | Sponsor Protocol Number: MK-7902-002 | Start Date*: 2019-01-21 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||
Full Title: Phase 3 Multicenter, Randomized, Double-blinded, Active-controlled, Clinical Study to Evaluate the Safety and Efficacy of Lenvatinib (E7080/MK- 7902) in Combination with Pembrolizumab (MK-3475) Ver... | |||||||||||||
Medical condition: Advanced hepatocellular carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) IE (Completed) ES (Completed) DE (Completed) PL (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-005386-67 | Sponsor Protocol Number: 20140318 | Start Date*: 2017-03-27 | ||||||||||||||||
Sponsor Name:Amgen Inc. | ||||||||||||||||||
Full Title: A Phase 1b/2, Multicenter, Open-label, Basket Trial to Evaluate the Safety of Talimogene Laherparepvec Injected into Liver Tumors Alone and in Combination With Systemic Pembrolizumab in Phase 1b an... | ||||||||||||||||||
Medical condition: Hepatocellular carcinoma (HCC) and metastatic liver tumors (non-HCC) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) DE (Completed) AT (Completed) PL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-005086-41 | Sponsor Protocol Number: B1030-101 | Start Date*: 2022-12-06 | ||||||||||||||||||||||||||
Sponsor Name:SOTIO Biotech Inc | ||||||||||||||||||||||||||||
Full Title: A First-in-Human, Phase 1/2, Dose Escalation Study of BOXR1030 T cells in Subjects With Advanced GPC3-Positive Solid Tumors. | ||||||||||||||||||||||||||||
Medical condition: Histologically confirmed advanced unresectable or metastatic hepatocellular carcinoma (HCC), squamous cell carcinoma (SCC) of the lung, myxoid/round cell liposarcoma, or Merkel cell carcinoma (MCC)... | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
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