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CRC clinical trials

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NCT ID: NCT05976282 Completed - Colorectal Cancer Clinical Trials

Addressing Colorectal Cancer in South Florida Firefighters

Start date: March 15, 2016
Phase: N/A
Study type: Interventional

The standard way of screening for colorectal cancer is to have a series of fecal blood tests, where a sample is taken from a participant's stool, or an endoscopic procedure performed by a doctor, where a camera is used to look inside the bowel. This research study will use a test performed by the participant. This test will look for changes in the stool that can identify if participants are at higher risk for cancer. Another aim of this study is to better understand what firefighters and retired firefighters think about colorectal cancer and other health issues. This information will help us develop programs that may improve colorectal cancer outcomes in the firefighter community.

NCT ID: NCT03965845 Completed - Solid Tumors Clinical Trials

A Study of Telaglenastat (CB-839) in Combination With Palbociclib in Patients With Solid Tumors

Start date: June 25, 2019
Phase: Phase 1/Phase 2
Study type: Interventional

This is a Phase 1b/2 study to determine the recommended phase 2 dose (RP2D), safety and tolerability, pharmacokinetics (PK) and clinical activity of the glutaminase inhibitor telaglenestat (CB-839) with the CDK4/6 Inhibitor, palbociclib in participants with advanced/metastatic solid tumors.

NCT ID: NCT03665285 Completed - Breast Cancer Clinical Trials

A Safety and Tolerability Study of NC318 in Subjects With Advanced or Metastatic Solid Tumors

Start date: October 1, 2018
Phase: Phase 1/Phase 2
Study type: Interventional

This research study is studying a new drug, NC318, as a possible treatment for advanced or metastatic solid tumors.

NCT ID: NCT03385980 Completed - NSCLC Stage IV Clinical Trials

Donation of Post Mortem Tumor Tissues

DONUM
Start date: February 11, 2016
Phase:
Study type: Observational

DONUM is an observational prospective independent protocol for patients with advanced lung cancer, colorectal cancer or cancer of unknown primary, willing to donate their tumor tissue samples post mortem for biomedical research purposes. All patients who fulfill the inclusion criteria will be eligible for the study after giving their Informed consent. Informed Consent will be obtained in two steps. During the pre-information step patients will be acquainted with the existence of a post-mortem cancer tissue donation research program governed by the DONUM protocol. If the patients manifest interest to participate into the program (in writing) during the pre-information step, they will proceed to step 2 and undergo the final informed consent process.

NCT ID: NCT03026075 Completed - CRC Clinical Trials

Evaluation of the Performance of the Motus Cleansing System (MCS)

MCS
Start date: December 22, 2016
Phase: N/A
Study type: Interventional

The study is multi-center study ,planned as a single arm, open trial, aimed at evaluating the performance and safety of a colon cleansing device during a colonoscopy procedure in a poorly prepared colons.

NCT ID: NCT02572076 Completed - CRC Clinical Trials

Clinical Investigational Plan: Evaluation of the Performance of the Motus Cleansing System

Start date: January 31, 2016
Phase: N/A
Study type: Interventional

The Motus GI Colon Cleansing device is intended to facilitate intra-procedural cleaning of a poorly prepared colon by irrigating the colon and evacuating the irrigation fluid and feces.

NCT ID: NCT02161549 Completed - CRC Clinical Trials

Evaluation of the Motus Gl CleanUp System During Screening Colonoscopy

Start date: July 2012
Phase: N/A
Study type: Observational [Patient Registry]

Motus Gl is developing a single-use device that attaches to a standard colonoscope, thereby integrating colon cleansing, screening and treatment into one procedure. The device creates turbulence within the colon using water jets. The colon's fecal fluids are evacuated by the system.

NCT ID: NCT01394939 Completed - Clinical trials for Colorectal Carcinoma

Recombinant Vaccinia Virus Administered Intravenously in Patients With Metastatic, Refractory Colorectal Carcinoma

Start date: January 2012
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to evaluate the safety, tolerability, and efficacy of JX-594 (Pexa-Vec) administered intravenously either alone or in combination with Irinotecan in colorectal carcinoma patients who are refractory to or intolerant to standard therapy.