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An Observational Study of Tarceva (Erlotinib) in Patients With Non-Small Cell Lung Cancer

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Roche

Status

Completed

Conditions

Non-Squamous Non-Small Cell Lung Cancer

Study type

Observational

Funder types

Industry

Identifiers

NCT01488331
ML22973

Details and patient eligibility

About

This prospective, multi-center, observational study will assess the progression-free survival and safety of patients with locally advanced or metastatic non-small cell lung cancer treated with Tarceva (erlotinib) and not disease progressing after at least 9 months. Data will be collected for 24 months.

Enrollment

217 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adult patients, >/=18 years of age
  • Diagnosis of locally advanced or metastatic non-small cell lung cancer (NSCLC, stage III/IV)
  • Treatment with Tarceva monotherapy and not progressing after at least 9 months at the date of study start

Exclusion criteria

  • Not agreeing to be followed-up (for a maximum of 24 months)

Trial design

217 participants in 1 patient group

Cohort

Trial contacts and locations

92

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Data sourced from clinicaltrials.gov

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