Source: ClinicalTrials.gov — U.S. National Library of Medicine — A database of privately and publicly funded clinical studies conducted around the world (U.S. National Library of Medicine, public domain).
This page lists clinical trials related to Liver Cancer from the ClinicalTrials.gov database.
Trial Summary
- Total studies: 50
- Recruiting: 21
- Active, not recruiting: 7
- Completed: 7
- Other: 15
Results are refreshed periodically and may not reflect the most current information available from ClinicalTrials.gov.
Recruiting Trials
NCT00001532 — Role of Genetic Factors in the Development of Lung Disease
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Heart, Lung, and Blood Institute (NHLBI) |
| Enrollment | 3500 |
| Study Type | OBSERVATIONAL |
| Conditions | Cystic Fibrosis; Pulmonary Fibrosis; Tuberous Sclerosis; Asthma; Pulmonary Sarcoidosis |
This study is designed to evaluate the genetics involved in the development of lung disease by surveying genes involved in the process of breathing and examining the genes in lung cells of patients with lung disease.
The study will focus on defining the distribution of abnormal genes responsible for processes directly involved in different diseases affecting the lungs of patients and healthy v…
NCT06342440 — Early Detection of Advanced Adenomas and Colorectal Cancer
| Status | Recruiting |
| Phase | N/A |
| Sponsor | City of Hope Medical Center |
| Enrollment | 2000 |
| Study Type | OBSERVATIONAL |
| Conditions | Colorectal Cancer; Colorectal Neoplasms; Colorectal Polyp; Colorectal Adenocarcinoma; Colorectal Disorders |
| Interventions |
This study aims to develop a highly sensitive, specific, and cost-effective blood assay for early detection of colorectal adenomas and cancer, using advanced machine learning and state-of-the-art biological analyses.
NCT04634357 — ET140203 T Cells in Pediatric Subjects With Hepatoblastoma, HCN-NOS, or Hepatocellular Carcinoma
| Status | Recruiting |
| Phase | Phase 1 / Phase 2 |
| Sponsor | Eureka Therapeutics Inc. |
| Enrollment | 12 |
| Study Type | INTERVENTIONAL |
| Conditions | Hepatoblastoma; Hepatocellular Carcinoma (HCC); Liver Neoplasms; Metastatic Liver Cancer; Liver Cancer |
| Interventions |
Open-label, dose escalation, multi-center, Phase I/II clinical trial to assess the safety/tolerability and determine the recommended Phase II Dose (RP2D) of ET140203 T-cells in pediatric subjects who are AFP-positive/HLA-A2-positive and have relapsed/refractory HB, HCN-NOS, or HCC.
NCT06184152 — CEUS vs. AMRI for HCC Detection in Patients With Indeterminate Liver Nodules
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of Texas Southwestern Medical Center |
| Enrollment | 600 |
| Study Type | INTERVENTIONAL |
| Conditions | HCC; Hepatocellular Carcinoma |
| Interventions | ; |
The study will be conducted at the following locations:
- UT Southwestern Medical Center
- Parkland Health and Hospital System
- University of Michigan
Investigators will prospectively compare the performance of dynamic contrast enhanced abbreviated MRI (AMRI) and contrast-enhanced ultrasound for early-stage HCC detection in patients with indeterminate liver nodules.
NCT06342414 — An Exosome-Based Liquid Biopsy for the Differential Diagnosis of Primary Liver Cancer
| Status | Recruiting |
| Phase | N/A |
| Sponsor | City of Hope Medical Center |
| Enrollment | 400 |
| Study Type | OBSERVATIONAL |
| Conditions | Hepatocellular Carcinoma; Intrahepatic Cholangiocarcinoma; Cholangiocarcinoma; Primary Liver Cancer; Primary Liver Carcinoma |
| Interventions |
It is sometimes difficult to precisely understand whether a primary liver cancer is a hepatocellular carcinoma or a cholangiocarcinoma. The researchers will develop and validate a liquid biopsy, based on exosomal content analysis and powered by machine learning, to help clinicians differentiate these two cancers before surgery.
NCT06260943 — Targeted Navigation in Hepatocellular Carcinoma (HCC)
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of Miami |
| Enrollment | 210 |
| Study Type | INTERVENTIONAL |
| Conditions | Hepatocellular Carcinoma; Cholangiocarcinoma; Hepatobiliary Cancer |
| Interventions |
The investigators are trying to learn more about the personal perceptions and experiences regarding the needs of patients with liver cancer to help improve the care of all patients. The investigators would like to know whether there are needs that patients have or are aware of, especially those needs that the investigators have not been able to address. The investigators aim to develop a progra…
NCT07224724 — Exosome-derived Extrahepatic Metastasis Detection By Liquid Biopsy In Colorectal Cancer Liver Metastases
| Status | Recruiting |
| Phase | N/A |
| Sponsor | City of Hope Medical Center |
| Enrollment | 500 |
| Study Type | OBSERVATIONAL |
| Conditions | Colorectal Cancer Liver Metastases (CRLM); Metastatic Colorectal Carcinoma (mCRC) |
| Interventions |
Colorectal cancer is the third most common malignancy worldwide, and prognosis largely depends on how effectively metastatic disease is managed. The liver is the most frequent and prognostically important site of metastasis, and patients responding well to chemotherapy may become candidates for curative hepatic resection. However, the presence of extrahepatic metastasis (EHM) critically influen…
NCT07224750 — A Noninvasive and Screening miRNA Signature for Gastrointestinal Cancer
| Status | Recruiting |
| Phase | N/A |
| Sponsor | City of Hope Medical Center |
| Enrollment | 1000 |
| Study Type | OBSERVATIONAL |
| Conditions | Hepatocellular Carcinoma (HCC); Cholangiocarcinoma; Pancreatic Ductal Adenocarcinoma (PDAC); Esophageal Squamous Cell Carcinoma (ESCC); Gastric Cancer (GC) |
Gastrointestinal (GI) cancers remain a major global health burden, largely due to the lack of effective and accessible early screening strategies. Current diagnostic approaches-including endoscopy, computed tomography (CT), and magnetic resonance imaging (MRI)-are either invasive, resource-intensive, or insufficiently sensitive for detecting early-stage disease, and are therefore not suitable f…
NCT06050252 — Testing the Combination of the Anticancer Drug Durvalumab With Chemotherapy (Gemcitabine and Cisplatin) at Improving Outcomes for High-Risk Resectable Liver Cancer Before Surgery
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 27 |
| Study Type | INTERVENTIONAL |
| Conditions | Resectable Intrahepatic Cholangiocarcinoma |
| Interventions | ; ; |
This phase II trial tests how well giving durvalumab with standard chemotherapy, gemcitabine and cisplatin, before surgery works in treating patients with high risk liver cancer (cholangiocarcinoma) that can be removed by surgery (resectable). Durvalumab is a monoclonal antibody that may interfere with the ability of tumor cells to grow and spread. Chemotherapy drugs, such as gemcitabine and ci…
NCT06427941 — A Phase 1 Study of BGB-B2033, Alone or in Combination With Tislelizumab With or Without Bevacizumab, in Participants With Advanced or Metastatic Solid Tumors
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | BeOne Medicines |
| Enrollment | 392 |
| Study Type | INTERVENTIONAL |
| Conditions | Metastatic Hepatocellular Carcinoma; Local Advanced Hepatocellular Carcinoma; Alpha-fetoprotein (AFP)-Producing Gastric Cancer; Extragonadal Yolk Sac Tumors; Glypican-3 (GPC3)-Positive Squamous Non-small Cell Lung Cancer |
| Interventions | ; ; |
This is a first-in-human (FIH) clinical study designed to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD), and anti-tumor activity of BGB-B2033 administered as monotherapy and in combination with tislelizumab, with or without bevacizumab. The study will enroll participants with locally advanced or metastatic hepatocellular carcinoma (HCC), alpha-fetoprotein (AFP)…
NCT06486454 — Real-world Evaluation of the HistoSonics Edison System for Treatment of Liver Tumors Across Multidisciplinary Users (BOOMBOX: Master Study)
| Status | Recruiting |
| Phase | N/A |
| Sponsor | HistoSonics, Inc. |
| Enrollment | 5000 |
| Study Type | OBSERVATIONAL |
| Conditions | Liver Neoplasms; Primary Liver Cancer; Secondary Liver Cancer; Tumor Liver; Benign Liver Tumor |
| Interventions |
The goal of this observational study is to collect information on the use of the HistoSonics Edison System for the treatment of liver tumors. The main aim is to understand how different patient characteristics and procedural characteristics may affect histotripsy success at 36 hours post-histotripsy procedure. Sub-studies to the BOOMBOX: Master Study will investigate specific populations and/or…
NCT06788002 — LDRT and Chemoimmunotherapy in NPC With Liver Metastasis
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Hunan Cancer Hospital |
| Enrollment | 26 |
| Study Type | INTERVENTIONAL |
| Conditions | Nasopharyngeal Cancinoma (NPC) |
| Interventions |
This study aims to evaluate the efficacy and toxicity of adding low-dose radiotherapy to chemoimmunotherapy as a first-line treatment for nasopharyngeal carcinoma patients with liver metastasis.
NCT06995898 — The Vanguard Study: Testing a New Way to Screen for Cancer
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 24000 |
| Study Type | INTERVENTIONAL |
| Conditions | Bladder Carcinoma; Breast Carcinoma; Colorectal Carcinoma; Esophageal Carcinoma; Gastric Carcinoma |
| Interventions | ; ; |
The Vanguard Study is a feasibility study to explore several aspects of evaluating multi-cancer detection (MCD) tests in a future definitive randomized controlled trial. An MCD test measures markers in the blood in order to screen for multiple cancers simultaneously. There is a need to understand how MCDs may work as cancer screening tools. The goal of cancer screening is to reduce the burden o…
NCT07159048 — The Safety, Efficacy, and Immune Response of Multimodal Thermal Therapy in the Treatment of Malignant Liver Tumors
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Fudan University |
| Enrollment | 120 |
| Study Type | INTERVENTIONAL |
| Conditions | Hepatocellular Carcinoma; Colorectal Cancer Liver Metastasis |
| Interventions | ; |
Multimodal thermal therapy (MTT), as an initiative integration of cryotherapy and radiofrequency heating, has been applied to treat various solid tumors. The feasibility and safety for MTT in the treatment of malignant liver tumors is well-established. This prospective, multi-center, randomized controlled clinical study aimed to explore the ablation-induced immune activating response of MTT in …
NCT06066138 — A Study of Therapeutic Drug Monitoring-Based Atezolizumab Dosing
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Locally Advanced Alveolar Soft Part Sarcoma; Metastatic Alveolar Soft Part Sarcoma; Locally Advanced Non Small Cell Lung Cancer; Metastatic Non Small Cell Lung Cancer; Locally Advanced Small Cell Lung Cancer |
| Interventions |
Background:
A type of drug called monoclonal antibody immune checkpoint inhibitors are often used in cancer treatment. These drugs help the body s immune system fight cancer by blocking proteins that cause cancer cells to grow. One of these drugs (atezolizumab) is approved to treat certain cancers. Researchers want to find out if lower doses of this drug might provide the same benefit with few…
NCT07227012 — Symbiotic-GI-13: A Study to Learn About Study Medicine Called PF-08634404 as a Single Treatment and Combination Treatment in Adult Participants With a Liver Cancer Called Hepatocellular Carcinoma, That is Too Advanced to be Removed by Surgery and May Have Spread to Other Parts of the Body.
| Status | Recruiting |
| Phase | Phase 1 / Phase 2 |
| Sponsor | Pfizer |
| Enrollment | 138 |
| Study Type | INTERVENTIONAL |
| Conditions | Carcinoma, Hepatocellular; Hepatocellular Cancer; Hepatocellular Carcinoma; Unresectable Hepatocellular Carcinoma; Liver Neoplasms |
| Interventions | ; |
The purpose of this study is to learn about the effects of study medicine (PF-08634404) when given alone or with another antibody (ipilimumab) for the treatment of a type of liver cancer called hepatocellular carcinoma (HCC) that is either locally advanced (spread to nearby tissues) or has spread to other parts of the body.
To join the study, participants must meet the following conditions:
*…
NCT06990659 — Outpatient Versus Inpatient Care Pathway for Intra-arterial Treatment of Primary Liver Cancer (CHOC)
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University Hospital, Angers |
| Enrollment | 206 |
| Study Type | INTERVENTIONAL |
| Conditions | Hepato Cellular Carcinoma (HCC); Intrahepatic Cholangiocarcinoma |
| Interventions | ; |
Randomized multicentre trial comparing two care organisations (ambulatory vs conventional inpatient) for patients undergoing transarterial chemoembolization (TACE) or radioembolization (TARE) for primary liver cancer (Hepato Cellular Carcinoma (HCC) or intrahepatic cholangiocarcinoma (iCCA)). Patients are followed for 7 months to assess patient satisfaction, safety and clinical outcomes. A qual…
NCT07343960 — A Phase I Study to Investigate the Pharmacokinetics and Safety of Capivasertib in Participants With Moderate Hepatic Impairment
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | AstraZeneca |
| Enrollment | 20 |
| Study Type | INTERVENTIONAL |
| Conditions | Moderate Hepatic Impairment |
| Interventions |
The purpose of this study is to measure the pharmacokinetics (PK), safety, and tolerability of capivasertib in participants with moderate hepatic impairment and participants with normal hepatic function (as control).
NCT07337525 — A First in Human Study of PLT012 in Participants With Solid Tumor Cancers
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | Pilatus Biosciences Inc |
| Enrollment | 36 |
| Study Type | INTERVENTIONAL |
| Conditions | Advanced Malignant Solid Tumor; Solid Tumor Cancer |
| Interventions |
The goal of this clinical trial is to learn about what doses of PLT012 are safe to use in adults with advanced cancers in solid tumors. It will also learn about how effective different doses of PLT012 are in treating cancer. The main questions it aims to answer are:
What adverse events and toxicities (harmful side effects) are associated with different doses of PLT012? What are the blood level…
NCT07507643 — A Study of Methylprednisolone in People Having Liver Surgery
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Memorial Sloan Kettering Cancer Center |
| Enrollment | 750 |
| Study Type | INTERVENTIONAL |
| Conditions | Hepatectomy |
| Interventions |
The purpose of this study is to test whether receiving methylprednisolone before surgery will reduce the side effects of having surgery, such as infections and longer hospital stays.
NCT07459309 — Clinical Study on the Safety, Efficacy, and Exploration of Immune Mechanisms of a Combined Multimodal Tumor Therapy System for Hepatic Malignancies
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Fudan University |
| Enrollment | 20 |
| Study Type | INTERVENTIONAL |
| Conditions | Liver Cancer (Primary and Metastatic); Liver Ablation |
| Interventions |
Clinical Study on the Safety, Efficacy, and Exploration of Immune Mechanisms of a Combined Multimodal Tumor Therapy System for Hepatic Malignancies
Active, Not Recruiting
NCT02465060 — Targeted Therapy Directed by Genetic Testing in Treating Patients With Advanced Refractory Solid Tumors, Lymphomas, or Multiple Myeloma (The MATCH Screening Trial)
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 6452 |
| Study Type | INTERVENTIONAL |
| Conditions | Advanced Lymphoma; Advanced Malignant Solid Neoplasm; Bladder Carcinoma; Breast Carcinoma; Cervical Carcinoma |
| Interventions | ; ; |
This phase II MATCH screening and multi-sub-trial studies how well treatment that is directed by genetic testing works in patients with solid tumors, lymphomas, or multiple myelomas that may have spread from where it first started to nearby tissue, lymph nodes, or distant parts of the body (advanced) and does not respond to treatment (refractory). Patients must have progressed following at leas…
NCT04175912 — Testing the Combination of Pevonedistat With Chemotherapy for Bile Duct Cancer of the Liver
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 40 |
| Study Type | INTERVENTIONAL |
| Conditions | Metastatic Cholangiocarcinoma; Metastatic Hepatocellular Carcinoma; Stage III Hepatocellular Carcinoma AJCC v8; Stage III Intrahepatic Cholangiocarcinoma AJCC v8; Stage IIIA Hepatocellular Carcinoma AJCC v8 |
| Interventions | ; ; |
This phase II trial studies how well pevonedistat alone or in combination with chemotherapy (paclitaxel and carboplatin) works in treating patients with bile duct cancer of the liver. Pevonedistat may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Chemotherapy drugs, such as paclitaxel and carboplatin, work in different ways to stop the growth of tumor ce…
NCT05211323 — A Study to Determine Whether Chemotherapy and Atezolizumab is Better Than Chemotherapy, Bevacizumab and Atezolizumab in Patients With Advanced Liver Cancer
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 88 |
| Study Type | INTERVENTIONAL |
| Conditions | Combined Hepatocellular Carcinoma and Cholangiocarcinoma; Stage III Liver Cancer; Stage IV Liver Cancer |
| Interventions | ; ; |
This phase II trial compares the effect of adding bevacizumab and atezolizumab to gemcitabine and cisplatin (chemotherapy) versus chemotherapy and atezolizumab in treating patients with liver cancer that cannot be removed by surgery (unresectable) or that may have spread from where it first started to nearby tissue, lymph nodes, or distant parts of the body (advanced). Immunotherapy with monocl…
NCT05724563 — Domvanalimab and Zimberelimab in Advanced Liver Cancers
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | University of Texas Southwestern Medical Center |
| Enrollment | 58 |
| Study Type | INTERVENTIONAL |
| Conditions | Hepatobiliary Cancer; Liver Cancer; Cholangiocarcinoma; Hepatocellular Carcinoma |
| Interventions | ; |
The goal of this clinical trial is to learn about advanced liver and bile duct cancers. The main question it aims to answer is:
If the combination of Domvanalimab and Zimberelimab are effective in treating advanced hepatobiliary cancers that have failed prior treatment.
NCT06117891 — An Observational Study to Learn More About How Well a Treatment Works When Given After Treatment With Atezolizumab and Bevacizumab or Another Similar Combination of Drugs in Adults With Liver Cancer That Cannot be Treated With Surgery
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Bayer |
| Enrollment | 300 |
| Study Type | OBSERVATIONAL |
| Conditions | Unresectable Hepatocellular Carcinoma |
| Interventions | ; ; |
This is an observational study in which only data will be collected from adults with unresectable hepatocellular carcinoma. These adults should be prescribed a different treatment after treatment with atezolizumab and bevacizumab, or another similar combination of drugs, by their doctors.
Unresectable hepatocellular carcinoma (uHCC) is a type of liver cancer that cannot be treated with surgery…
NCT06859840 — LEAF(Liver Tumor dEtection And classiFication AI)
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Zhejiang University |
| Enrollment | 1528 |
| Study Type | INTERVENTIONAL |
| Conditions | Hepatocellular Carcinoma |
| Interventions |
This study plans to utilize multiphase contrast-enhanced and non-contrast CT(Computed Tomography) images from 10000 pathologically confirmed liver tumor patients at our hospital. An AI(artificial intelligence) model will be used to outline the 3D contours of liver masses, which will then be refined by radiologists and hepatobiliary-pancreatic surgeons to enhance model accuracy. By incorporating…
NCT07118176 — Determining the Biodistribution of an Imaging Tracer (68Ga-FAPi-46) in Patients With Solid Tumors or Hematologic Cancers
| Status | Active, not recruiting |
| Phase | Phase 1 |
| Sponsor | Jonsson Comprehensive Cancer Center |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Anal Carcinoma; Bladder Carcinoma; Breast Carcinoma; Cervical Carcinoma; Cholangiocarcinoma |
| Interventions | ; ; |
This phase I trial is evaluating a new imaging tracer (68Ga-FAPi-46) with positron emission tomography (PET)/computed tomography (CT) to determine where and to which degree the tracer (68Ga-FAPi-46) accumulates in normal and cancer tissues (the biodistribution) in patients with solid tumors or hematologic (blood) cancers. PET is an established imaging technique that utilizes small amounts of ra…
Not Yet Recruiting
NCT07676383 — Precision Navigation to Improve Community Cancer Screening Participation
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Hunan Cancer Hospital |
| Enrollment | 1500 |
| Study Type | INTERVENTIONAL |
| Conditions | Cancer Screening; Lung Cancer; Breast Cancer; Colorectal Cancer; Upper Gastrointestinal Cancer |
| Interventions | ; |
This study will evaluate whether a precision navigation intervention can help community residents at high risk for cancer complete recommended cancer screening. The study will be conducted in communities participating in an urban cancer screening program in China.
Eligible participants will be adults aged 45 to 74 years who are permanent residents of participating communities and have been ide…
NCT07446257 — THIO and Cadonilimab in Resectable Hepatocellular Carcinoma
| Status | Not yet recruiting |
| Phase | Early Phase 1 |
| Sponsor | University of Texas Southwestern Medical Center |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | Resectable Hepatocellular Carcinoma |
| Interventions | ; |
The goal of this clinical study is to find out if cadonilimab or ateganosine plus cadonilimab is effective and safe in treating resectable hepatocellular carcinoma (HCC).
NCT07685535 — HAIC + DEB-TACE + Toripalimab + Lenvatinib for Unresectable Intrahepatic Cholangiocarcinoma
| Status | Not yet recruiting |
| Phase | Phase 2 |
| Sponsor | Shanghai Zhongshan Hospital |
| Enrollment | 29 |
| Study Type | INTERVENTIONAL |
| Conditions | Liver Cancer |
| Interventions | ; ; |
Purpose: This phase II clinical trial evaluates whether a combination of liver-directed local therapies (HAIC and DEB-TACE) with immunotherapy (toripalimab) and targeted therapy (lenvatinib) is safe and effective for patients with unresectable intrahepatic cholangiocarcinoma (a type of liver cancer that cannot be removed by surgery).
Participants: Adults aged 18-85 years with pathologically co…
NCT07685548 — AI-Driven Tumor Response Evaluation for Solid Tumors
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Shanghai Zhongshan Hospital |
| Enrollment | 6120 |
| Study Type | OBSERVATIONAL |
| Conditions | Solid Tumor Cancer; Neoplasms; Hepatocellular Carcinoma |
| Interventions |
Purpose: This study is developing and validating an artificial intelligence (AI)-driven system to evaluate tumor response using changes in total tumor volume. The goal is to determine whether this AI-based approach can better predict patient survival compared with the current standard method (RECIST), which relies on linear measurements of a few selected tumors.
Participants: The study include…
NCT07675187 — HCC Risk and Monitoring in Patients With Type 2 Diabetes
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | National Taiwan University Hospital |
| Enrollment | 2400 |
| Study Type | INTERVENTIONAL |
| Conditions | Type 2 Diabetes (T2DM); Hepatocellular Carcinoma (HCC) |
| Interventions |
Liver cancer is a significant malignancy in Taiwan. With the widespread implementation of antiviral therapies, hepatitis B and C-related liver cancer has gradually declined; however, metabolic dysfunction-associated liver cancer continues to increase, particularly among patients with type 2 diabetes mellitus (T2DM) who also present with significant liver fibrosis. Current clinical guidelines la…
NCT07681817 — Risk Stratification and Proactive Nursing Intervention for Acute Kidney Injury Following Interventional Therapy in Patients With Liver Cancer
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Tianjin Medical University Cancer Institute and Hospital |
| Enrollment | 200 |
| Study Type | INTERVENTIONAL |
| Conditions | Liver Cancer, Adult |
| Interventions | ; |
This study focuses on the early identification and precision prevention of acute kidney injury (AKI) following interventional therapy in patients with liver cancer. A prospective, phased mixed-methods research design will be adopted. In the first phase, a prospective cohort study will be conducted to systematically collect clinical and nursing-related data. A Super Learner ensemble algorithm wi…
NCT07627191 — GLP-1 RA Plus SOC Treatment in First-line, Metastatic Pancreatic, Colorectal, or Hepatocellular Cancer
| Status | Not yet recruiting |
| Phase | Early Phase 1 |
| Sponsor | University of Arizona |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Pancreatic Cancer; Colorectal Cancer; Hepatocellular Carcinoma |
| Interventions |
There is a growing number of patients diagnosed with gastrointestinal cancers who are also simultaneously being treated with GLP-1 Receptor Agonists (RA)s. To date, no clinical trial data exists to establish safety and/or feasibility with use of GLP-1 RAs during chemotherapy in the metastatic setting. The goal of this clinical trial is to evaluate the safety, tolerability, preliminary efficacy,…
NCT07687914 — A Study of IMM2510 + IMM27M Combination Therapy in Patients With Advanced Hepatocellular Carcinoma
| Status | Not yet recruiting |
| Phase | Phase 2 |
| Sponsor | ImmuneOnco Biopharmaceuticals (Shanghai) Inc. |
| Enrollment | 50 |
| Study Type | INTERVENTIONAL |
| Conditions | HCC - Hepatocellular Carcinoma |
| Interventions |
This is a Phase 2, open-label, multicenter,study designed to evaluate the safety, tolerability, pharmacokinetics, and preliminary antitumor activity of IMM2510(Anti-PD-L1 and VEGF trap recombinant - Page 1 of 5 - protein) combine with IMM27M(Anti-CTLA-4 Humanized monoclonal antibody) in patients with advanced hepatocellular carcinoma who not have received the treatment for aHCC in past
NCT07684040 — A Study of Combination Therapy in Patients With Resectable Liver Cancer
| Status | Not yet recruiting |
| Phase | Phase 2 |
| Sponsor | Affiliated Hospital of Guangdong Medical University |
| Enrollment | 68 |
| Study Type | INTERVENTIONAL |
| Conditions | Liver Cancer (Primary and Metastatic) |
| Interventions |
This is a prospective, single-arm clinical study designed to evaluate the efficacy and safety of an initial combination treatment strategy followed by surgery in patients with cancer. Eligible participants will receive combination therapy prior to surgical intervention. Patients who meet predefined surgical criteria will undergo hepatic resection. Following surgery, additional treatment may be …
NCT07682454 — Utilize Imaging to Assess Changes in Hepatocellular Carcinoma Perfusion as Potentiated by Intra-Arterial Nitroglycerin
| Status | Not yet recruiting |
| Phase | Phase 2 |
| Sponsor | University of California, San Francisco |
| Enrollment | 50 |
| Study Type | INTERVENTIONAL |
| Conditions | Hepatocellular Carcinoma (HCC); Liver Cancer, Adult |
| Interventions | ; ; |
This is a single-arm, open-label, single-center, first-in-human feasibility study evaluating parenchymal blood volume (PBV) imaging as a tool to dynamically assess perfusional changes in hepatocellular carcinoma (HCC) potentiated by intra-arterial administration of nitroglycerin.
NCT07690683 — Patients With Hepatocellular Carcinoma (HCC)
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Fondazione Policlinico Universitario Agostino Gemelli IRCCS |
| Enrollment | 52 |
| Study Type | INTERVENTIONAL |
| Conditions | Hepatocellular Carcinoma; Hepatocellular Cancer; Liver Diseases; Liver Cancer |
| Interventions | ; |
Hepatocellular carcinoma (HCC) is one of the leading causes of cancer-related mortality worldwide and is frequently diagnosed at an advanced stage, resulting in limited therapeutic options. Despite the advances in immunotherapy, a substantial proportion of patients fail to respond adequately due to mechanisms of immune resistance. The gut microbiota plays a crucial role in modulating the respon…
NCT07689175 — Adaptive Dosing of Immune Checkpoint Inhibitors for Hepatocellular Carcinoma
| Status | Not yet recruiting |
| Phase | Phase 2 |
| Sponsor | University of Texas Southwestern Medical Center |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | Hepatocellular Carcinoma (HCC) |
| Interventions | ; |
The goal of this clinical trial is to learn if immunotherapy including nivolumab plus ipilimumab is effective and safe in treating hepatocellular carcinoma.
Completed Trials
NCT01387555 — A Phase 2b Study of Modified Vaccinia Virus to Treat Patients Advanced Liver Cancer Who Failed Sorafenib
| Status | Completed |
| Phase | Phase 2 |
| Sponsor | Jennerex Biotherapeutics |
| Enrollment | 129 |
| Study Type | INTERVENTIONAL |
| Conditions | Hepatocellular Carcinoma; Liver Cancer; HCC |
| Interventions | ; |
This study is to determine whether JX-594 (Pexa-Vec) plus best supportive care is more effective in improving survival than best supportive care in patients with advanced Hepatocellular Carcinoma (HCC) who have failed sorafenib.
NCT07687758 — Non-Invasive Risk Stratification for Hepatocellular Carcinoma in HCV-Related Compensated Advanced Chronic Liver Disease Following Sustained Virological Response: Validation of the aMAP Score
| Status | Completed |
| Phase | N/A |
| Sponsor | Siriraj Hospital |
| Enrollment | 571 |
| Study Type | OBSERVATIONAL |
| Conditions | Hepatitis C Virus Infection; Compensated Advanced Chronic Liver Disease; Hepatocellular Carcinoma (HCC) |
| Interventions |
This retrospective cohort study evaluated the performance of non-invasive risk scores for predicting de novo hepatocellular carcinoma in adults with hepatitis C virus-related compensated advanced chronic liver disease who achieved sustained virological response after sofosbuvir-based direct-acting antiviral therapy. Patients treated at Siriraj Hospital between 2013 and 2023 were included if the…
NCT02344680 — Liver Fibrosis in Zambian HIV-HBV Co-infected Patients
| Status | Completed |
| Phase | N/A |
| Sponsor | University of Alabama at Birmingham |
| Enrollment | 349 |
| Study Type | OBSERVATIONAL |
| Conditions | Human Immunodeficiency Virus; HBV; Fibrosis, Liver; Cirrhosis, Liver; Hepatocellular Carcinoma |
| Interventions |
A cohort of adults with HIV-HBV co-infection will be created in Lusaka, Zambia, to describe the short and long-term (up to 10 years of follow-up) HBV and liver outcomes, including the effectiveness of current therapies, and to identify the risk factors for major endpoints of interest, including HCC and HBV functional cure. This cohort will also create a pool of potential participants for in-dep…
NCT03519997 — A Study of Pembrolizumab and Bavituximab in Patients With Advanced Hepatocellular Carcinoma
| Status | Completed |
| Phase | Phase 2 |
| Sponsor | David Hsieh |
| Enrollment | 35 |
| Study Type | INTERVENTIONAL |
| Conditions | Hepatocellular Carcinoma |
| Interventions | ; |
This is a non-randomized, open-label, multi-site phase II therapeutic trial of pembrolizumab and bavituximab in patients with locally advanced HCC. Locally advanced or metastatic HCC is defined as disease that is not amenable to surgical and/or locoregional therapies. Subjects must not have received prior systemic therapy for advanced HCC in keeping with the first-line setting of this study.
NCT03472586 — Ipilimumab and Nivolumab With Immunoembolization in Treating Participants With Metastatic Uveal Melanoma in the Liver
| Status | Completed |
| Phase | Phase 2 |
| Sponsor | Sidney Kimmel Comprehensive Cancer Center at Thomas Jefferson University |
| Enrollment | 14 |
| Study Type | INTERVENTIONAL |
| Conditions | Metastatic Malignant Neoplasm in the Liver; Metastatic Uveal Melanoma; Stage IV Uveal Melanoma AJCC v7 |
| Interventions | ; ; |
This phase II trial studies ipilimumab and nivolumab with immunoembolization in treating patients with uveal melanoma that has spread to the liver. Immunotherapy with monoclonal antibodies, such as ipilimumab and nivolumab, may help the body’s immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread. Immunoembolization may kill tumor cells due to los…
NCT05249426 — A Study to Test Whether Different Combinations of BI 765063, Ezabenlimab, Chemotherapy, Cetuximab, and BI 836880 Help People With Head and Neck Cancer or Liver Cancer
| Status | Completed |
| Phase | Phase 1 |
| Sponsor | Boehringer Ingelheim |
| Enrollment | 48 |
| Study Type | INTERVENTIONAL |
| Conditions | Head and Neck Squamous Cell Carcinoma (HNSCC) |
| Interventions | ; ; |
With an amendment of the protocol, this study is only open to adults with head and neck cancer. Previously also adults with liver cancer joined. This is a study for people for whom previous treatment was not successful or no standard treatment exists. The purpose of this study is to find out whether combining different medicines make tumours shrink.
The tested medicines in this study are antib…
NCT06935149 — Detecting Colorectal Cancer With Liver Metastatic Lesions Using Novel Precise Imaging Tools
| Status | Completed |
| Phase | Phase 1 |
| Sponsor | Primo Biotechnology Co., Ltd |
| Enrollment | 5 |
| Study Type | INTERVENTIONAL |
| Conditions | Liver Metastasis Colon Cancer |
| Interventions |
This study will demonstrate the diagnostic utility of PSMA PET among patients with CRC with liver metastasis.
Other (Suspended)
NCT02506946 — NAFLD in Adolescents and Young Adults With PCOS
| Status | Suspended |
| Phase | N/A |
| Sponsor | Columbia University |
| Enrollment | 80 |
| Study Type | OBSERVATIONAL |
| Conditions | Polycystic Ovary Syndrome; Non-Alcoholic Fatty Liver Disease; Metabolic Syndrome |
This project focuses on an at-risk adolescent and young adult population who may gain long-term health benefits from detection of risk factors at a young age. The primary aims of this proposal are: 1) To observe whether adolescents and young adults with Polycystic Ovary Syndrome (PCOS) are more likely to have elevated liver fat (>/=4.8%) than controls by studying liver fat deposition measured …
Other (Terminated)
NCT05705791 — Clinical Investigation Evaluating Safety and Efficacy of Selective Intra-arterial 166Holmium Radiation Therapy in Combination With Atezolizumab and Bevacizumab for Non Resectable Hepatocellular Carcinoma
| Status | Terminated |
| Phase | N/A |
| Sponsor | Gustave Roussy, Cancer Campus, Grand Paris |
| Enrollment | 10 |
| Study Type | INTERVENTIONAL |
| Conditions | Hepatocellular Carcinoma |
| Interventions |
The goal of this clinical trial is to evaluate the added value of 166Holmium SIRT to Atezolizumab-Bevacizumab in patients with non resectable HCC. The primary endpoint is the Best Objective Response Rate at 6 months after 166Holmium SIRT according to mRECIST.
Participants will be treated by :
- Approved first line systemic therapy: Atezolizumab (1200mg Q3W, IV) with Bevacizumab (15mg/kg Q3W, …
NCT05797870 — Selective Internal Radiation Therapy and 188Re-SSS Lipiodol Treatment for Liver Cancer (Lip-Re2)
| Status | Terminated |
| Phase | Phase 2 |
| Sponsor | Center Eugene Marquis |
| Enrollment | 16 |
| Study Type | INTERVENTIONAL |
| Conditions | Hepatocellular Carcinoma Non-resectable |
| Interventions |
The goal of this monocentric interventional study is to evaluate the efficacy, in terms of objective response rate, of the 188Re-SSS lipiodol SIRT in patients with non-operable HCC.