Clinical Trials Directory

Trials / Unknown

UnknownNCT01196260

Combination Chemotherapy Treatments in Patients With Colorectal Cancer Stage II and III

Clinical Trial on Combination Chemotherapy Treatments in Patients With Colorectal Cancer Stage II and III Among Chinese Population

Status
Unknown
Phase
Phase 2 / Phase 3
Study type
Interventional
Enrollment
8,000 (estimated)
Sponsor
State Key Laboratory of Cancer Biology · Network
Sex
All
Age
18 Years – 90 Years
Healthy volunteers
Not accepted

Summary

This study will examine a new combination of drugs: Capecitabine and Oxaliplatin for the treatment of Stage II and III colorectal cancer. Capecitabine and Oxaliplatin are approved by the Food and Drug Administration (FDA) for use in colorectal cancer. The combination of drugs is experimental (not approved by the FDA as standard treatment), but is a widely used treatment option and preliminary studies have shown that treatment with the combination has a positive effect on metastatic colorectal cancer.

Detailed description

This study will examine a new combination of drugs: Capecitabine and Oxaliplatinfor for the treatment of Stage II and III colorectal cancer. Capecitabine and Oxaliplatin are approved by the Food and Drug Administration (FDA) for use in colorectal cancer. The combination of drugs is experimental (not approved by the FDA as standard treatment), but is a widely used treatment option and preliminary studies have shown that treatment with the combination has a positive effect on metastatic colorectal cancer. In the present trial, we will study the combination of these two drugs in patients with colorectal cancer among Chinese population

Conditions

Interventions

TypeNameDescription
DRUGCapecitabine and OxaliplatinCapecitabine and Oxaliplatin will be under the NSCLC guideline

Timeline

Start date
2004-01-01
Primary completion
2020-12-01
Completion
2020-12-01
First posted
2010-09-08
Last updated
2018-02-20

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT01196260. Inclusion in this directory is not an endorsement.