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Metastatic Colon Cancer clinical trials

View clinical trials related to Metastatic Colon Cancer.

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NCT ID: NCT04322539 Active, not recruiting - Clinical trials for Metastatic Colorectal Cancer

A Study of Efficacy and Safety of Fruquintinib (HMPL-013) in Participants With Metastatic Colorectal Cancer

FRESCO-2
Start date: August 12, 2020
Phase: Phase 3
Study type: Interventional

This is a global, randomized, double-blind, placebo-controlled, multicenter phase 3 clinical trial to compare the efficacy and safety of fruquintinib plus best supportive care (BSC) versus placebo plus BSC in participants with refractory metastatic colorectal cancer (mCRC). 691 participants were randomized to one of the following treatment arms in a 2:1 ratio, fruquintinib plus BSC or placebo plus BSC.

NCT ID: NCT03251378 Active, not recruiting - Rectal Cancer Clinical Trials

A Multi-Center, Open-Label Study of Fruquintinib in Solid Tumors, Colorectal, and Breast Cancer

Start date: November 10, 2017
Phase: Phase 1
Study type: Interventional

An open-label, dose escalation and expansion clinical trial to evaluate the safety, tolerability, and PK of fruquintinib in patients with advanced solid tumors, metastatic colorectal cancer and metastatic breast cancer.

NCT ID: NCT02724202 Active, not recruiting - Clinical trials for Metastatic Colon Cancer

Curcumin in Combination With 5FU for Colon Cancer

Start date: March 2016
Phase: Early Phase 1
Study type: Interventional

The purpose of this study is to test the safety and find the response rate of combining the dietary supplement, curcumin, with the standard of care, FDA-approved chemotherapy drug 5-fluorouracil (5FU, Adracil) and see what effects (good and bad) that the combined treatments have on colon cancer.

NCT ID: NCT02254941 Active, not recruiting - Clinical trials for Metastatic Colon Cancer

Observational Study to Evaluate the Use of Targeted Therapies in Metastatic Colorectal Cancer

Start date: August 2014
Phase:
Study type: Observational

The purpose of this study is to evaluate, in terms of overall survival, the benefit of monoclonal antibodies in the start time of the diagnosis of advanced disease or administer a deferred basis after progression to treatment with chemotherapy alone. Initially expected target population was 1950 patients (pts), in 2015 protocol was ammended to 1028 patients, because the size was sufficient to evaluate the superiority of the use of monoclonal antibodies the start time of the diagnosis against deferred use, with HR of 0.8, power of 90% and an alpha of 0.05. Finally in July 2018, recruitment was completed with a total of 1104 patients enrolled.

NCT ID: NCT00986661 Active, not recruiting - Clinical trials for Hepatocellular Carcinoma

A Study to Assess PV-10 Chemoablation of Cancer of the Liver

Start date: October 2009
Phase: Phase 1
Study type: Interventional

This open-label study will evaluate the safety, tolerability, pharmacokinetics and effect on tumor growth following a single intralesional injection of PV-10 in subjects with either (a) hepatocellular carcinoma (HCC) that is not amenable to resection, transplant or other potentially curative therapy or (b) cancer metastatic to the liver.