Drug Use Investigation for TYKERB Tablet (All Case Investigation)

NCT01332396 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 4054

Last updated 2017-04-26

No results posted yet for this study

Summary

Data on the safety and efficacy of TYKERB shall be collected from the patients in order to grasp the actual conditions of post-marketing use and assess background information on the patients.

Conditions

Interventions

DRUG

Lapatinib

Sponsors & Collaborators

Principal Investigators

  • Novartis Pharmaceuticals · Novartis Pharmaceuticals

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-06-30
Primary Completion
2017-03-13
Completion
2017-03-13

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Entities

Diseases
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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 NCT01332396 on ClinicalTrials.gov