Regulatory TYKERB® Tablets PMS

NCT00975988 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 750

Last updated 2014-10-27

No results posted yet for this study

Summary

Non-interventional, open-label, single group, multicentric post-marketing surveillance to monitor the safety and effectiveness of TYKERB® tablets administered in Korean patients according to the prescribing information TYKERB® is a registered trademark of the GlaxoSmithKline group of companies.

Conditions

Interventions

DRUG

TYKERB® tablets

Patients administrated TYKERB® tablets according to the prescribing information

Sponsors & Collaborators

Principal Investigators

  • GSK Clinical Trials · GlaxoSmithKline

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-01-31
Primary Completion
2014-07-31
Completion
2014-07-31

Countries

  • South Korea

Study Locations

More Related Trials

Entities

Diseases

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 NCT00975988 on ClinicalTrials.gov