Study of Chemotherapy Combined With Nimotuzumab in Untreated Metastatic Nasopharyngeal Carcinoma

NCT01616849 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 39

Last updated 2015-09-22

No results posted yet for this study

Summary

This is an open-label, uncontrolled, multicenter phase II clinical trial. The purpose of this study is to evaluate acute toxicity and efficacy of cisplatin and 5-Fu combined with nimotuzumab in patients with untreated metastatic nasopharyngeal carcinoma.

Conditions

  • Stage IV Nasopharyngeal Carcinoma

Interventions

DRUG

cisplatin and 5-Fu combined with nimotuzumab

DDP+5-Fu DDP 100 mg/m2 intravenous infusion in day1, 5-Fu 1000mg/m2/d continuous intravenous infusion on days 1 through 4, both drugs are given every 3 weeks. Nimotuzumab 200mg/d, intravenous infusion every week

Sponsors & Collaborators

  • Fujian Cancer Hospital

    collaborator OTHER_GOV
  • First People's Hospital of Foshan

    collaborator OTHER
  • People's Hospital of Guangxi Zhuang Autonomous Region

    collaborator OTHER
  • Guangxi Medical University

    collaborator OTHER
  • Guangzhou Medical University

    collaborator OTHER
  • Hubei Cancer Hospital

    collaborator OTHER
  • Hunan Provincial Cancer Hospital

    collaborator UNKNOWN
  • Hangzhou Cancer Hospital

    collaborator OTHER
  • Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

    collaborator OTHER
  • Tongji Hospital

    collaborator OTHER
  • Jiangxi Provincial Cancer Hospital

    collaborator OTHER
  • Affiliated Cancer Hospital of Shantou University Medical College

    collaborator OTHER
  • Wuhan University

    collaborator OTHER
  • Zhejiang Cancer Hospital

    collaborator OTHER
  • Sun Yat-sen University

    lead OTHER

Principal Investigators

  • Chong Zhao, MD · Sun Yat-sen University

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-05-31
Primary Completion
2015-07-31
Completion
2015-07-31

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01616849 on ClinicalTrials.gov