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An Observational Study of Tarceva (Erlotinib) in Routine Practice For First Line Maintenance Therapy in Patients With Non Small Cell Lung Cancer

Roche logo

Roche

Status

Completed

Conditions

Non-Squamous Non-Small Cell Lung Cancer

Study type

Observational

Funder types

Industry

Identifiers

NCT01194050
ML22816

Details and patient eligibility

About

This observational study will investigate the tolerability and efficacy of Tarceva (erlotinib) in daily clinical practice under routine conditions in patients with locally advanced or metastatic non small cell lung cancer. Data will be collected for approximately 12 months.

Enrollment

289 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adult patients with locally advanced or metastatic non-small cell lung cancer (stage IIIb or IV) with stable disease after 4 cycles of standard platinum-based first-line chemotherapy

Exclusion criteria

  • Not willing or not able to sign written informed consent form

Trial design

289 participants in 1 patient group

Cohort

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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