Safety of Xeloda in Solid Tumours

NCT02479217 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1268

Last updated 2017-02-17

No results posted yet for this study

Summary

The primary objective of this study is to observe safety and tolerability of Xeloda as used in medical practice, alone and in combination with docetaxel.

Conditions

  • Metastatic Breast Cancer, Colon Cancer

Interventions

DRUG

Docetaxel

DRUG

Xeloda

Sponsors & Collaborators

Principal Investigators

  • Clinical Trials · Hoffmann-La Roche

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-07-31
Primary Completion
2009-06-30
Completion
2009-06-30

Countries

  • Serbia

Study Locations

More Related Trials

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 NCT02479217 on ClinicalTrials.gov