FOLFOX4 Combined With Endostar in Patients With Advanced Colorectal Cancer

A Multi-center Study of Folfox4 Combined With Recombinant Human Endostatin(Endostar)in Advanced Colorectal Cancer

Status

UNKNOWN

Phases

Phase 2

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT00813137

Enrollment

120

Registered

2008-12-22

Start date

2008-10-31

Completion date

2010-10-31

Last updated

2009-12-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colorectal Neoplasms

Keywords

Colorectal Cancer, chemotherapy, recombinant human endostatin

Brief summary

FOLFOX4 plus Avastin has been suggested as firstline regimen for advanced colorectal cancer by NCCN, a new angiogenesis inhibitor, known as Endostar(Recombinant Human Endostatin), prolonged the overall survival, time to progression and improved response rate in metastatic lung cancer in a large phase III clinical trial in china, so we design this trial to evaluate the safty and efficacy of FolFox4 plus Endostar in patients with advanced colorectal cancer

Detailed description

Endostar is free supported by Shangdong Simcere Medgene biotech co.,Ltd. Endostar combination with Chemotherapy has been the first line treatment regimen to advanced NSCLC. Clinical data proved that Endostar was a wild spectrum and safe antiangiogenesis factor which could suppress almost 65 kinds of tumor mass in animal models and affect about 12 percent human genome. China NCCN colon or rectal cancer clinical practice guideline recommends Chemotherapy plus angiogenesis inhibitor as the first line treatment scheme. So we design FOLFOX4 plus Endostar to treat advanced colorectal cancer to research the RR and safety. We believe this treatment regimen may be a new approach to the advanced colorectal cancer patients.

Interventions

DRUGFolfox4 plus recombinant human endostatin (Endostar)

Endostar 15mg iv drip D1\ 7, D15\ 21, Oxaliplatin 85mg/m2 iv drip D1,15, CF 200mg/m2 iv drip D1,2,15,16, 5-Fu 400mg/m2 iv D1,2,15,16, 5-Fu 600mg/m2 civ D1,2,15,16

Study design

Allocation

Intervention model

SINGLE_GROUP

Primary purpose

TREATMENT

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

18 Years to 75 Years

Healthy volunteers

Inclusion criteria

* Patients with histologically or cytologically confirmed metastatic CRC * Measurable disease according to Response Criteria In Solid Tumours (RECIST) * Performance Status 0 - 2 according to ECOG (Eastern Cooperative Oncology Group) Performance Status * Age 18\ 75 * Life expectancy \> 3 months * Signed informed consent (IC) * Adequate haematological and biological functions

Exclusion criteria

* Pregnant or lactating women * Known immediate or delayed hypersensitivity reaction or idiosyncrasy to drugs chemically related to the study drugs * Neuropathy, brain, or leptomeningeal involvement * Treatment with any biologic, cytotoxic, radiation , or hormonal therapy within four weeks. * Clinically relevant coronary artery disease or a history of a myocardial infarction within the last 12 months or high risk/uncontrolled arrhythmia * Uncontrolled significant comorbid conditions and previous radiotherapy

Design outcomes

Primary

Measure	Time frame
Time to progression	every two cycles

Countries

China

Contacts

Primary ContactYang Ling, M.D. Ph.D.

medilyn2001@yahoo.com.cn

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026