Effect of Osimertinib in Ethnic Chinese With EGFR and T790M Mutated NSCLC

NCT03133234 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 47

Last updated 2018-11-20

No results posted yet for this study

Summary

To assess the effectiveness and safety of osimertinib treatment in a real world setting.

Conditions

  • T790M Positive NSCLC Patients

Interventions

DRUG

osimertinib

Oral dose of 80mg once daily

Sponsors & Collaborators

Principal Investigators

  • Yabing Cao · Kiang Wu Hospital

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-05-23
Primary Completion
2017-09-13
Completion
2017-09-13
FDA Drug
Yes

Countries

  • China

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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 NCT03133234 on ClinicalTrials.gov