Clinical Trials for Intestinal Cancer

Currently registered clinical trials for Intestinal Cancer from ClinicalTrials.gov. 26 recruiting, 50 total studies.

This content is for informational purposes only. Always consult a healthcare professional.

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 Intestinal Cancer from the ClinicalTrials.gov database.

Trial Summary

  • Total studies: 50
  • Recruiting: 26
  • Active, not recruiting: 10
  • Completed: 5
  • Other: 9

Results are refreshed periodically and may not reflect the most current information available from ClinicalTrials.gov.

Recruiting Trials

NCT01174121 — Immunotherapy Using Tumor Infiltrating Lymphocytes for Patients With Metastatic Cancer

StatusRecruiting
PhasePhase 2
SponsorNational Cancer Institute (NCI)
Enrollment332
Study TypeINTERVENTIONAL
ConditionsMetastatic Colorectal Cancer; Metastatic Pancreatic Cancer; Metastatic Ovarian Cancer; Metastatic Breast Carcinoma; Metastatic Endocrine Tumors/ Neuroendocrine Tumors
Interventions; ;

Background:

The NCI Surgery Branch has developed an experimental therapy that involves taking white blood cells from patients’ tumors, growing them in the laboratory in large numbers, and then giving the cells back to the patient. These cells are called Tumor Infiltrating Lymphocytes, or TIL and we have given this type of treatment to over 200 patients with melanoma. Researchers want to know i…

NCT01915225 — Obtaining Solid Tumor Tissue From People Having Biopsy or Surgery for Certain Types of Cancer

StatusRecruiting
PhaseN/A
SponsorNational Cancer Institute (NCI)
Enrollment1800
Study TypeOBSERVATIONAL
ConditionsColorectal Neoplasms; Gastric Neoplasms; Cholangiocarcinoma; Bile Duct Cancer; Pancreas Cancer

Background:

- Recent advances in cancer research have led to new therapies to treat the disease. It is important to continue these advances and discover new ones. To do that, researchers need tissue samples from solid tumors. This study will collect such samples from people already scheduled to have a procedure at the National Institutes of Health Clinical Center (NIHCC).

Objectives:

- To …

NCT02595957 — Genomic Services Research Program

StatusRecruiting
PhaseN/A
SponsorNational Human Genome Research Institute (NHGRI)
Enrollment5000
Study TypeOBSERVATIONAL
ConditionsColon Cancer; Breast Cancer

Background:

Genes are the instructions a person s body uses to function. Genome sequencing reads through all of a person s genes. Everyone has many gene variants, and most do not cause disease. Some gene variants called secondary findings may be important for a person s health even if they are not related to the reason why a person had genome sequencing done. Researchers want to learn more abo…

NCT03805919 — Men at High Genetic Risk for Prostate Cancer

StatusRecruiting
PhaseN/A
SponsorNational Cancer Institute (NCI)
Enrollment500
Study TypeOBSERVATIONAL
ConditionsProstatic Neoplasms

Background:

Research studies have shown that genetic changes and family history may increase a man s risk for prostate cancer. Researchers want to follow the prostate health of men who have specific genetic changes associated with prostate cancer to help them learn more about which men are at higher risk for prostate cancer.

Objectives:

To study men with specific genetic changes and determin…

NCT04222413 — Metarrestin (ML-246) in Subjects With Metastatic Solid Tumors

StatusRecruiting
PhasePhase 1
SponsorNational Cancer Institute (NCI)
Enrollment116
Study TypeINTERVENTIONAL
ConditionsAdvanced Solid Tumors; Metastatic Pancreatic Cancer; Pediatric Solid Tumor; Advanced Breast Cancer; Malignant Peripheral Nerve Sheath Tumor
Interventions

Background:

Metastasis is the spread of cancer from one organ to a nonadjacent organ. It causes 90% of cancer deaths. No treatment specifically prevents or reduces metastasis. Researchers hope a new drug can help. It stops cancer cells from growing and spreading further and possibly shrink cancer lesions in distant organs.

Objective:

To find a safe dose of metarrestin and to see if this dose…

NCT04847063 — Individual Response to Hyperthermic Intraperitoneal Chemotherapy (HIPEC) Treatment of Peritoneal Carcinomatosis From Peritoneal Mesothelioma or Atypical Mesothelial Proliferation or From Ovarian, Colorectal, or Appendiceal Histologies

StatusRecruiting
PhasePhase 1
SponsorNational Cancer Institute (NCI)
Enrollment60
Study TypeINTERVENTIONAL
ConditionsPeritoneal Mesothelioma; Peritoneal Carcinomatosis; Ovarian Cancer; Gastrointestinal Cancer; Appendiceal Cancer
Interventions; ;

Background:

Cytoreductive surgery (CRS) removes tumors in the abdomen. HIPEC is hyperthermic (heated) chemotherapy that washes the inside of the abdomen. CRS with HIPEC may help people with peritoneal carcinomatosis. These are tumors that have spread to the lining of the abdomen from other cancers. Researchers think they can improve the results of CRS with HIPEC treatment on these tumors by ch…

NCT06342401 — Early Onset Colorectal Cancer Detection

StatusRecruiting
PhaseN/A
SponsorCity of Hope Medical Center
Enrollment400
Study TypeOBSERVATIONAL
ConditionsColorectal Cancer; Colorectal Neoplasms; Colorectal Adenocarcinoma; Colorectal Cancer Stage I; Colorectal Cancer Stage IV
Interventions

Colorectal cancer (CRC) once predominantly affected older individuals, but in recent years has witnessed a progressive increase in incidence among young adults. Once rare, early-onset colorectal cancer (EOCRC, that is, a CRC diagnosed before the age of 50) now constitutes 10-15% of all newly diagnosed CRC cases and it stands as the first cause of cancer-related death in young men and the second…

NCT07224724 — Exosome-derived Extrahepatic Metastasis Detection By Liquid Biopsy In Colorectal Cancer Liver Metastases

StatusRecruiting
PhaseN/A
SponsorCity of Hope Medical Center
Enrollment500
Study TypeOBSERVATIONAL
ConditionsColorectal 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…

NCT07224815 — cfDNA 5mC/5hmC Biomarkers to Predict Chemotherapy Response in Metastatic Colorectal Cancer

StatusRecruiting
PhaseN/A
SponsorCity of Hope Medical Center
Enrollment600
Study TypeOBSERVATIONAL
ConditionsCRC (Colorectal Cancer)
Interventions;

The EpiCORE study aims to identify cfDNA-based epigenetic markers predictive of response to first-line chemotherapy (FOLFOX or FOLFIRI) in metastatic colorectal cancer (mCRC).

By integrating 5-methylcytosine (5mC) and 5-hydroxymethylcytosine (5hmC) profiling, this study seeks to establish a non-invasive biomarker panel capable of distinguishing responders from non-responders.

NCT07224841 — Development of a cfDNA 5mC/5hmC-based Biomarker Panel to Predict Targeted Therapy Efficacy in mCRC

StatusRecruiting
PhaseN/A
SponsorCity of Hope Medical Center
Enrollment500
Study TypeOBSERVATIONAL
ConditionsCRC (Colorectal Cancer)
Interventions;

The EpiDRIVE study aims to identify cfDNA-based epigenetic determinants of response in metastatic colorectal cancer (mCRC) patients treated with EGFR- or VEGF-targeted therapy.

By integrating 5-methylcytosine (5mC) and 5-hydroxymethylcytosine (5hmC) profiling, this study seeks to develop a predictive biomarker panel capable of differentiating responders from non-responders to targeted therapy.

NCT07226115 — Splicing-based Predictive Learning for Individual Chemotherapy Evaluation in Colorectal Cancer

StatusRecruiting
PhaseN/A
SponsorCity of Hope Medical Center
Enrollment200
Study TypeOBSERVATIONAL
ConditionsColorectal Cancer; Colorectal Cancer Recurrent; Colorectal Cancer Stage II; Colorectal Cancer Stage III
Interventions

Colorectal cancer (CRC) remains one of the leading causes of cancer-related mortality worldwide. Although adjuvant chemotherapy improves survival after curative resection, its efficacy varies widely among patients. The absence of reliable predictive biomarkers often leads to overtreatment or undertreatment.

This study aims to develop a machine learning-based predictive model for adjuvant chemo…

NCT06562192 — Phase I Study of [177Lu]Lu-NNS309 in Patients With Pancreatic, Lung, Breast and Colorectal Cancers

StatusRecruiting
PhasePhase 1
SponsorNovartis Pharmaceuticals
Enrollment162
Study TypeINTERVENTIONAL
ConditionsPancreatic Ductal Adenocarcinoma; Non-small Cell Lung Cancer; HR+/HER2- Ductal and Lobular Breast Cancer; Triple Negative Breast Cancer; Colorectal Cancer
Interventions;

The purpose of this study is to evaluate the safety, tolerability, dosimetry and preliminary efficacy of [177Lu]Lu-NNS309 and the safety and imaging properties of [68Ga]Ga-NNS309 in patients aged ≥ 18 years with locally advanced or metastatic pancreatic ductal adenocarcinoma (PDAC), non-small cell lung cancer (NSCLC), HR+/HER2- ductal and lobular breast cancer (BC), triple negative breast c…

NCT06562543 — A Trial to Evaluate the Safety and Activity of Fruquintinib in Minority Populations With Advanced, Previously Treated Colorectal Cancer

StatusRecruiting
PhasePhase 4
SponsorTakeda
Enrollment78
Study TypeINTERVENTIONAL
ConditionsColorectal Cancer
Interventions

High blood pressure (hypertension) is a known side effect of the treatment with fruquintinib. Current research does not provide a clear answer whether minority groups such as Black/African American and/or Hispanic/Latino with refractory metastatic colorectal cancer (mCRC) have a bigger risk of higher blood pressure after treatment with fruquintinib. The main aim of this study is to learn how of…

NCT07255729 — An Exosomal microRNA Signature for Preoperative Staging in Colon Cancer

StatusRecruiting
PhaseN/A
SponsorCity of Hope Medical Center
Enrollment400
Study TypeOBSERVATIONAL
ConditionsColon Cancer
Interventions;

Recent studies have highlighted the potential benefits of neoadjuvant chemotherapy (NAC) in colon cancer; however, its indication is generally limited to cases corresponding to pathological stage IIB or higher. Accurately identifying such high-risk cases before surgery remains challenging using conventional clinical diagnostics alone. Therefore, we hypothesized that integrating molecular biomar…

NCT06760819 — A Study to Learn More About How Well Treatment With Sevabertinib (BAY 2927088) Tablets Works and How Safe it is in Participants Who Have a Solid Tumor With Mutations of the Human Epidermal Growth Factor Receptor 2 (HER2)

StatusRecruiting
PhasePhase 2
SponsorBayer
Enrollment111
Study TypeINTERVENTIONAL
ConditionsAdvanced Solid Tumors; HER2 Mutation
Interventions

Researchers are looking for a better way to treat people who have solid tumors with HER2-activating mutations. Before a treatment can be approved for people to take, researchers do clinical trials to better understand its safety and how it works.

In this trial, the researchers want to learn how well BAY2927088 (sevabertinib) works in people with different types of solid tumors with HER2 mutati…

NCT06995898 — The Vanguard Study: Testing a New Way to Screen for Cancer

StatusRecruiting
PhaseN/A
SponsorNational Cancer Institute (NCI)
Enrollment24000
Study TypeINTERVENTIONAL
ConditionsBladder 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…

NCT06696768 — Clinical Trial of an Anti-cancer Drug, CA-4948 (Emavusertib), in Combination With Chemotherapy Treatment (FOLFOX Plus Bevacizumab) in Metastatic Colorectal Cancer

StatusRecruiting
PhasePhase 1
SponsorNational Cancer Institute (NCI)
Enrollment24
Study TypeINTERVENTIONAL
ConditionsMetastatic Colorectal Adenocarcinoma; Stage III Colorectal Cancer AJCC v8; Stage IV Colorectal Cancer AJCC v8; Unresectable Colorectal Adenocarcinoma
Interventions; ;

This phase I trial studies the side effects and best dose of CA-4948 when given together with fluorouracil, leucovorin, oxaliplatin (FOLFOX) plus bevacizumab in treating patients with colorectal cancer that has spread from where it first started (primary site) to other places in the body (metastatic). CA-4948 may stop the growth of tumor cells by blocking some of the enzymes needed for cell gro…

NCT07114601 — A Study of LY4257496 in Participants With Cancer (OMNIRAY)

StatusRecruiting
PhasePhase 1
SponsorEli Lilly and Company
Enrollment421
Study TypeINTERVENTIONAL
ConditionsBreast Neoplasms; Colorectal Neoplasms; Prostate Neoplasm; Endometrial Neoplasms; Neoplasm Metastasis
Interventions; ;

The main purpose of this study is to evaluate safety, tolerability, and efficacy of LY4257496 alone and as part of relevant standard of care (SOC) combination therapy in participants with Gastrin-releasing Peptide Receptor (GRPR)-positive advanced cancer, including but not limited to breast, colorectal, prostate, endometrial, esophageal, gastroesophageal (GE) junction, and gastric cancer. The s…

NCT07213791 — A Study of LY4337713 in Participants With FAP-Positive Solid Tumors

StatusRecruiting
PhasePhase 1
SponsorEli Lilly and Company
Enrollment241
Study TypeINTERVENTIONAL
ConditionsOvarian Neoplasms; Breast Neoplasms; Pancreatic Intraductal Neoplasms; Colorectal Neoplasms; Esophageal Neoplasms
Interventions

This is a study of LY4337713 in participants with certain types of cancer that is advanced or has spread. Participants must have cancer with high levels of a protein called fibroblast activation protein (FAP). The purpose of this study is to evaluate safety, side effects, and efficacy of LY4337713. In addition, this study will evaluate how much LY4337713 gets into the bloodstream, how it is bro…

NCT07296887 — CARE Tool Study Aim 3

StatusRecruiting
PhaseN/A
SponsorWashington University School of Medicine
Enrollment430
Study TypeINTERVENTIONAL
ConditionsGynecologic Cancer; Prostate Cancer; Lung Cancer; Colorectal Cancer
Interventions; ;

This study is a multi-site randomized trial to study the implementation of the CARE Tool and evaluate the CARE Tool. The CARE Tool is a web-based tool that gives people information about cancer care costs, health insurance, and resources to help with costs. Overall, the study aims to help patients with cancer overcome barriers they face navigating insurance and accessing financial resources.

NCT07525206 — A Study to Access Intravenous (IV) Telisotuzumab Adizutecan in Combination With IV Bevacizumab Compared to Standard of Care IV Bevacizumabin Combination With Oral Trifluridine and Tipiracil in Adult Participants With Refractory Metastatic Colorectal Cancer

StatusRecruiting
PhasePhase 3
SponsorAbbVie
Enrollment700
Study TypeINTERVENTIONAL
ConditionsColorectal Cancer
Interventions; ;

Colorectal cancer (CRC) is the third most common type of cancer diagnosed worldwide. The purpose of this study is to assess the adverse events and change in disease activity of telisotuzumab adizutecan plus bevacizumab compared to standard of care (SOC) of LONSURF (trifluridine and tipiracil) plus bevacizumab in adult participants with c-Met over-expressed refractory metastatic colorectal cance…

NCT07406633 — KQB198 in Combination With Imatinib in Participants With Advanced/Metastatic GIST in 1st Line Setting (SynerGIST-1st Line)

StatusRecruiting
PhasePhase 2
SponsorKumquat Biosciences Inc.
Enrollment46
Study TypeINTERVENTIONAL
ConditionsGIST - Gastrointestinal Stromal Tumor; GIST; GIST Metastatic Cancer; Gastro Intestinal Stromal Tumour; Gastrointestinal Tumors
Interventions;

This study will test an experimental drug called KQB198 in combination with imatinib. The goal is to determine if this combination is safe and tolerable and assess how effective the combination is at treating GIST. Imatinib has been approved by the FDA for the treatment of different types of cancer including GIST.

NCT07676461 — Oral, Fecal and Intratumoral Microbiome Atlas in Colombian Patients With Advanced Solid Tumors Receiving First-Line Immunotherapy

StatusRecruiting
PhaseN/A
SponsorCentro de Tratamiento e Investigación sobre Cáncer, Luis Carlos Sarmiento Angulo
Enrollment150
Study TypeOBSERVATIONAL
ConditionsGastric Cancer; Colorectal Cancer; Breast Cancer; Cervical Cancer; Head and Neck Cancer (H&N)
Interventions

This is a prospective observational cohort study conducted at Fundación CTIC in Bogotá, Colombia. It characterizes the oral, fecal and intratumoral microbiome of Colombian adults with advanced solid tumors (gastric, colorectal, breast, cervical and head-and-neck cancer) who receive first-line immunotherapy as standard of care, and compares them with healthy volunteers. Using multi-omics (HiFi m…

NCT07687875 — Oncolytic Virotherapy to Enhance PReoperative IMmunotherapy Efficacy in Patients With Proficient Mismatch Repair (pMMR) Rectal Cancer

StatusRecruiting
PhasePhase 1
SponsorHenry Smith
Enrollment20
Study TypeINTERVENTIONAL
ConditionsRectal Cancer Patients
Interventions

A Phase I clinical trial that will investigate the safety and tolerability of combining the modified vaccinia virus BT-001 with systemic pembrolizumab in patients with localised pMMR rectal cancer

NCT07529808 — Phase 1/2 Study of BHB810 in Advanced Gastric and GEJ Adenocarcinoma

StatusRecruiting
PhasePhase 1 / Phase 2
SponsorBigHat Biosciences, Inc.
Enrollment164
Study TypeINTERVENTIONAL
ConditionsGastric Cancer; Gastric Adenocarcinoma; Gastric (Stomach) Cancer; Gastroesophageal Adenocarcinoma; Gastroesophageal Cancer (GC)
Interventions

This study is looking at how safe BHB810 is in adults with gastric and gastroesophageal adenocarcinoma (GEJ). The purpose of this study is also to look at: how well the study drug works, how the study drug moves into, through, and out of the body, and how your body reacts to the study drug. Participants will get an IV infusion of BHB810 every 2 weeks while on study treatment.

NCT07659795 — A Phase 2 Study of VS-7375 in Patients With KRAS G12D-Mutated Colorectal Cancer

StatusRecruiting
PhasePhase 2
SponsorVerastem, Inc.
Enrollment150
Study TypeINTERVENTIONAL
ConditionsColorectal Cancer
Interventions; ;

This study will assess the safety and efficacy of VS-7375 alone and in combination with cetuximab or panitumumab and cetuximab plus mFOLFOX in patients with metastatic KRAS G12D - mutated Colorectal Cancer

Active, Not Recruiting

NCT02484404 — Phase I/II Study of the Anti-Programmed Death Ligand-1 Durvalumab Antibody (MEDI4736) in Combination With Olaparib and/or Cediranib for Advanced Solid Tumors and Advanced or Recurrent Ovarian, Triple Negative Breast, Lung, Prostate and Colorectal Can…

StatusActive, not recruiting
PhasePhase 1 / Phase 2
SponsorNational Cancer Institute (NCI)
Enrollment268
Study TypeINTERVENTIONAL
ConditionsColorectal Neoplasms; Breast Neoplasms
Interventions; ;

Background:

- Durvalumab is a drug that may help people s immune systems respond to and kill cancer cells. Olaparib is a drug that may inhibit repairing DNA damage of cancer cells. Cediranib is a drug that may stop the blood vessel growth of cancer cells. This study has two components. In the phase 1 component of the study, researchers want to investigate how well participants tolerate the co…

NCT02465060 — Targeted Therapy Directed by Genetic Testing in Treating Patients With Advanced Refractory Solid Tumors, Lymphomas, or Multiple Myeloma (The MATCH Screening Trial)

StatusActive, not recruiting
PhasePhase 2
SponsorNational Cancer Institute (NCI)
Enrollment6452
Study TypeINTERVENTIONAL
ConditionsAdvanced 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…

NCT02997228 — Testing the Addition of Atezolizumab to Combination Chemotherapy or Atezolizumab Alone for Metastatic Colon or Rectal Cancer, the COMMIT Study

StatusActive, not recruiting
PhasePhase 3
SponsorNational Cancer Institute (NCI)
Enrollment120
Study TypeINTERVENTIONAL
ConditionsMetastatic Colorectal Adenocarcinoma; Stage IV Colorectal Cancer AJCC v7
Interventions; ;

This phase III trial studies how well combination chemotherapy, bevacizumab, and/or atezolizumab work in treating patients with deficient deoxyribonucleic acid (DNA) mismatch repair colorectal cancer that has spread from where it first started (primary site) to other places in the body (metastatic). Chemotherapy drugs, such as fluorouracil, oxaliplatin, and leucovorin calcium, work in different…

NCT04291105 — Phase 2 Trial of Voyager V1 in Combination With Cemiplimab in Cancer Patients

StatusActive, not recruiting
PhasePhase 2
SponsorVyriad, Inc.
Enrollment87
Study TypeINTERVENTIONAL
ConditionsMelanoma; Head and Neck Squamous Cell Carcinoma; Colo-rectal Cancer
Interventions;

This is a Phase 2 study designed to determine the preliminary anti-tumor activity and confirm the safety of VV1 in combination with cemiplimab. The study will enroll patients with three distinct separate tumor cohorts. The cancers types are colorectal, head and neck carcinoma, and melanoma that are progressing on CPI treatment. (CRC and melenoma cohorts are now closed to new patients)

NCT04521686 — Study of LY3410738 Administered to Patients With Advanced Solid Tumors With IDH1 or IDH2 Mutations

StatusActive, not recruiting
PhasePhase 1
SponsorEli Lilly and Company
Enrollment200
Study TypeINTERVENTIONAL
ConditionsCholangiocarcinoma; Chondrosarcoma; Glioma; Any Solid Tumor
Interventions; ;

This is an open-label, multicenter Phase 1 study to evaluate safety, tolerability and preliminary efficacy of oral LY3410738 in patients with isocitrate dehydrogenase 1 (IDH1) arginine 132 (R132)-mutant advanced solid tumors, including but not limited to cholangiocarcinoma, chondrosarcoma, and glioma or isocitrate dehydrogenase 2 (IDH2) arginine 140 (R140) or arginine 172 (R172) mutant cholangi…

NCT05308446 — Testing the Addition of Nivolumab to Standard Treatment for Patients With Metastatic or Unresectable Colorectal Cancer That Have a BRAF Mutation

StatusActive, not recruiting
PhasePhase 2
SponsorNational Cancer Institute (NCI)
Enrollment86
Study TypeINTERVENTIONAL
ConditionsMetastatic Colon Adenocarcinoma; Metastatic Rectal Adenocarcinoma; Stage III Colon Cancer AJCC v8; Stage III Rectal Cancer AJCC v8; Stage IV Colon Cancer AJCC v8
Interventions; ;

This phase II trial tests whether adding nivolumab to the usual treatment (encorafenib and cetuximab) works better than the usual treatment alone to shrink tumors in patients with colorectal cancer that has spread to other places in the body (metastatic) or that cannot be removed by surgery (unresectable) and whose tumor has a mutation in a gene called BRAF. Encorafenib is in a class of medicat…

NCT05628194 — ASSESSING THE GAY MALE EXPERIENCE WITH ANAL CANCER PREVENTION STRATEGIES

StatusActive, not recruiting
PhaseN/A
SponsorUniversity of Minnesota
Enrollment92
Study TypeOBSERVATIONAL
ConditionsAnal Cancer
Interventions

The purpose of this study is to describe current knowledge and opinions about anal cancer screening among men who have sex with men (MSM), as well as their experience receiving guideline-compliant care aimed at anal cancer risk reduction using a large-scale survey disseminated via social media.

NCT05396846 — MyGI Diet for Colorectal Cancer Prevention

StatusActive, not recruiting
PhaseN/A
SponsorUniversity of Michigan
Enrollment240
Study TypeINTERVENTIONAL
ConditionsColorectal Neoplasms
Interventions; ;

This study evaluates three different approaches that could help people eat in healthier ways. The study seeks to enroll 240 overweight and obese persons who have risk factors for colorectal cancers such as a family or personal history of colorectal cancers or adenomatous polyps. The study website is www.MyBestGI.org .

Participants in the study will be asked to follow one of three eating plans,…

NCT07224854 — Epigenetic Signature for CRC Early Detection

StatusActive, not recruiting
PhaseN/A
SponsorCity of Hope Medical Center
Enrollment500
Study TypeOBSERVATIONAL
ConditionsColorectal Cancer (Diagnosis); Non-cancer Controls; DNA Methylation; Cell Free DNA; Early Detection of Cancer

The epiCED is a noninvasive blood-based assay designed for early detection of colorectal cancer (CRC) using circulating cell-free DNA (cfDNA) 5-methylcytosine (5mC) and 5-hydroxymethylcytosine (5hmC) epigenetic markers. This study leverages retrospective, multi-center cohorts of CRC patients and non-cancer controls to discover and validate a robust cfDNA methylation signature. Small-scale seque…

NCT06147037 — A Phase 1, Dose-escalation Study of [225Ac]-FPI-2068 in Adult Patients With Advanced Solid Tumours

StatusActive, not recruiting
PhasePhase 1
SponsorAstraZeneca
Enrollment13
Study TypeINTERVENTIONAL
ConditionsAdvanced Solid Tumor; Metastatic Colorectal Carcinoma; Head and Neck Squamous Cell Carcinoma; Non-small Cell Lung Cancer; Pancreatic Ductal Adenocarcinoma
Interventions; ;

This is a first-in-human, Phase 1, non-randomized, multicenter, open-label clinical study designed to investigate the safety, tolerability, dosimetry, biodistribution, and pharmacokinetics (PK) of [225Ac]-FPI-2068, [111In]-FPI-2107, and FPI-2053 in metastatic and/or recurrent solid tumors (HNSCC, NSCLC, mCRC, PDAC, GC, RCC).

Not Yet Recruiting

NCT07676383 — Precision Navigation to Improve Community Cancer Screening Participation

StatusNot yet recruiting
PhaseN/A
SponsorHunan Cancer Hospital
Enrollment1500
Study TypeINTERVENTIONAL
ConditionsCancer 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…

NCT07689812 — A Multicenter Randomized Open-Label Trial Evaluating MRD-Guided Interruption Versus Standard of Care Immune-Checkpoint Inhibitor (ICI) Therapy In Patients With Advanced / Metastatic Solid Tumors.

StatusNot yet recruiting
PhaseN/A
SponsorNatera, Inc.
Enrollment920
Study TypeINTERVENTIONAL
ConditionsNSCLC (Advanced Non-small Cell Lung Cancer); NSCLC (Non-small Cell Lung Cancer); NSCLC (Non-small Cell Lung Carcinoma); NSCLC; Melanoma (Skin Cancer)
Interventions

This is an open-label, randomized study evaluating whether MRD-guided intermittent ICI therapy provides comparable survival to SOC continuous ICI therapy in subjects with histologically confirmed advanced / metastatic NSCLC, melanoma, MSI-High/dMMR CRC, RCC and other solid tumors. This study will be conducted in up to 100 sites.

Enrolling by Invitation

NCT07686133 — Digital Education in Colorectal Cancer Patients

StatusEnrolling by invitation
PhaseN/A
SponsorUniversity Health Network, Toronto
Enrollment100
Study TypeINTERVENTIONAL
ConditionsColorectal Cancer; Patient Satisfaction; Patient Engagement; Patient
Interventions

The goal of this clinical trial is to evaluate the impact of integrating video- based education in colorectal cancer surgery, with a specific focus on patient’s perspective. The main questions it aims to answer are:

Does addition of video-based patient education material lower patient’s anxiety around colorectal cancer surgery? Does it increase patient’s understanding of their diagnosis? Does …

NCT07328516 — Natural History Study of Early Life Exposures in Agriculture (ELEA)

StatusEnrolling by invitation
PhaseN/A
SponsorNational Cancer Institute (NCI)
Enrollment64277
Study TypeOBSERVATIONAL
ConditionsProstate Cancer; Leukemia; Breast Cancer; Melanoma; Colorectal Cancer

Study Description:

ELEA is an observational cohort study that will collect exposure information and biospecimens from the adult children of the Agricultural Health Study (AHS) cohort (https://aghealth.nih.gov/about; Protocol OH93NCN013).

The primary hypothesis is that early life exposures, particularly those found in the agricultural environment, are associated with cancer and other adverse h…

Completed Trials

NCT00040222 — Clinical, Genetic, Behavioral, Laboratory and Epidemiologic Characterization of Individuals and Families at High Risk of Breast/Ovarian Cancer

StatusCompleted
PhaseN/A
SponsorNational Cancer Institute (NCI)
Enrollment377
Study TypeOBSERVATIONAL
ConditionsFamilial Ovarian Cancer; Familial Breast Cancer; BRCA1-associate Malignancies; BRCA2-associated Malignancies

Individuals and families with known or suspected syndromes that include breast, ovarian or genetically-related cancers are enrolled in this family study, which is a syndrome-specific sub-set of the long-standing DCEG Human Genetics Program umbrella family studies protocol (78-C-0039). Cancer outcomes are documented through review of medical, vital, and pathology records. Selected individuals an…

NCT01380600 — Phase 1b Dose Escalation Study of Intravenous JX-594 in Metastatic, Refractory Colorectal Carcinoma

StatusCompleted
PhasePhase 1
SponsorJennerex Biotherapeutics
Enrollment15
Study TypeINTERVENTIONAL
ConditionsCarcinoma, Colorectal
Interventions

The purpose of this pilot safety study is to evaluate the safety and tolerability of JX-594 (Pexa-Vec) administered intravenously every 2 weeks in colorectal carcinoma patients who are refractory to or intolerant of oxaliplatin, irinotecan, and Erbitux treatments.

NCT03345563 — Project HERO: Health Empowerment & Recovery Outcomes

StatusCompleted
PhaseN/A
SponsorRutgers, The State University of New Jersey
Enrollment113
Study TypeINTERVENTIONAL
ConditionsProstate Cancer; Bladder Cancer; Kidney Cancer; Colon Cancer; Rectum Cancer
Interventions; ;

Project HERO is a 12-week study of the efficacy of Body Mind Training (BMT, i.e. Tai Chi and Qigong in this project) for reducing fatigue in male cancer survivors. This 3-arm randomized clinical trial will examine inflammatory biology and selected gene-expression pathways that are hypothesized to contribute to the intervention’s effect.

NCT03879109 — Chemotherapy Followed by Pelvic Reirradiation Versus Chemotherapy Alone as Pre-operative Treatment for Locally Recurrent Rectal Cancer

StatusCompleted
PhasePhase 3
SponsorUniversity Hospital, Bordeaux
Enrollment58
Study TypeINTERVENTIONAL
ConditionsRectal Cancer
Interventions; ;

GRECCAR 15 is focused on Locally Recurrent Rectal Cancer (LRRC) for patients with previous pelvic radiotherapy for the primary rectal cancer. This situation leads to a 20% higher risk of non-curative resection for the LRRC management (R1 status) impacting significantly the overall survival. The widespread use of neoadjuvant radiotherapy for primary rectal cancer introduces this new problem: the…

NCT06411756 — Physical Activity Centers Empowerment

StatusCompleted
PhaseN/A
SponsorUNC Lineberger Comprehensive Cancer Center
Enrollment21
Study TypeINTERVENTIONAL
ConditionsColorectal Neoplasms
Interventions; ;

This research study tests the feasibility of the Physical Activity Centers Empowerment (PACE) physical activity intervention for African American individuals diagnosed with colorectal cancer.

Feasibility will be measured as intervention reach, effectiveness, adoption, implementation, and maintenance. Seventy-two subjects will be recruited to conduct a pilot two-group, randomized repeated measu…

Available Studies

NCT07689942 — Expanded Access to 0.5 mg eRapa for Familial Adenomatous Polyposis

StatusAvailable
PhaseN/A
SponsorBiodexa Pharmaceuticals
EnrollmentN/A
Study TypeEXPANDED_ACCESS
ConditionsFamilial Adenomatous Polyposis (FAP)
Interventions

This expanded access program provides 0.5 mg eRapa (encapsulated rapamycin) to patients with familial adenomatous polyposis (FAP) who have no satisfactory alternative treatment options and are not eligible to participate in a clinical trial. The objective is to provide access to eRapa based on the treating physician’s assessment that the potential benefits outweigh the potential risks, with app…

Other (Suspended)

NCT06102902 — Testing the Addition of Anti-cancer Drug, ZEN003694, to the Usual Chemotherapy Treatment, Cetuximab Plus Encorafenib, for Colorectal Cancer

StatusSuspended
PhasePhase 1
SponsorNational Cancer Institute (NCI)
Enrollment30
Study TypeINTERVENTIONAL
ConditionsMetastatic Colorectal Adenocarcinoma; Recurrent Colorectal Adenocarcinoma; Refractory Colorectal Adenocarcinoma; Stage IV Colorectal Cancer AJCC v8
Interventions; ;

This phase I trial tests the safety, best dose, and effectiveness of ZEN003694 in combination with cetuximab and encorafenib in treating patients with colorectal cancer that has not responded to previous treatment (refractory), that has come back after a period of improvement (relapsed), and that has spread from where it first started (primary site) to other places in the body (metastatic). ZEN…

Other (Terminated)

NCT06466187 — A Study of SGN-MesoC2 in Advanced Solid Tumors

StatusTerminated
PhasePhase 1
SponsorSeagen, a wholly owned subsidiary of Pfizer
Enrollment19
Study TypeINTERVENTIONAL
ConditionsCarcinoma, Non-Small-Cell Lung; Ovarian Neoplasms; Pancreatic Adenocarcinoma; Colorectal Neoplasms; Mesothelioma
Interventions

This clinical trial is studying advanced solid tumors. Solid tumors are cancers that start in a part of your body like your lungs or liver instead of your blood. Once tumors have grown bigger in one place but haven’t spread, they’re called locally advanced. If your cancer has spread to other parts of your body, it’s called metastatic. When a cancer has gotten so big it can’t easily be removed o…

NCT07388563 — Azacitidine and Abatacept in Relapsed or Refractory T-Cell Lymphoma

StatusSuspended
PhasePhase 1
SponsorNational Cancer Institute (NCI)
Enrollment20
Study TypeINTERVENTIONAL
ConditionsLymphoma, T Cell, Peripheral; T-cell Lymphoma; Angioimmunoblastic T-cell Lymphoma; Anaplastic Large Cell Lymphoma; Monomorphic Epitheliotropic Intestinal T-cell Lymphoma
Interventions;

Background:

T-cell lymphoma is a blood cancer that affects immune system cells. People tend to survive less than 1 year if this disease does not respond to treatment (is refractory) or comes back after treatment (relapses). Azacitidine and abatacept are 2 drugs that are used to treat other diseases. Researchers want to know if these drugs, used together, can help people with T-cell lymphoma.

NCT06557733 — An Investigational Drug (TPST-1495) in Patients With Familial Adenomatous Polyposis

StatusSuspended
PhasePhase 2
SponsorNational Cancer Institute (NCI)
Enrollment38
Study TypeINTERVENTIONAL
ConditionsColorectal Carcinoma; Familial Adenomatous Polyposis
Interventions; ;

This open-label phase II trial tests how well TPST-1495 works in reducing the number of polyps in the small bowel and colon in patients with familial adenomatous polyposis (FAP). FAP is an inherited condition in which numerous polyps (growths that protrude from mucous membranes) form on the inside walls of the colon and rectum. It increases the risk for colon cancer. TPST-1495 binds to specific…