Post-marketing Surveillance Study of Docetaxel-Based Chemotherapy

NCT02972216 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 40

Last updated 2016-11-23

No results posted yet for this study

Summary

A Post-marketing Surveillance Study to Evaluate the Effectiveness and Safety of Docetaxel-Based Chemotherapy

Conditions

  • Nonsmall Cell Lung Cancer
  • Squamous Cell Carcinoma of the Head and Neck

Interventions

DRUG

Nolbaxol

DRUG

Taxotere

DRUG

cisplatin

Sponsors & Collaborators

  • Taichung Veterans General Hospital

    collaborator OTHER
  • National Cheng-Kung University Hospital

    collaborator OTHER
  • Tri-Service General Hospital

    collaborator OTHER
  • Yung Shin Pharm. Ind. Co., Ltd.

    lead INDUSTRY

Eligibility

Min Age
20 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-11-30
Primary Completion
2016-10-31

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Entities

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 NCT02972216 on ClinicalTrials.gov