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CompletedNCT01836133

An Observational Study of Tarceva (Erlotinib) in Participants With Locally Advanced or Metastatic Adenocarcinoma Non-Small Cell Lung Cancer (ELEMENT)

Efficacy and Safety of Erlotinib (Tarceva® ) Therapy in Patients With Locally Advanced or Metastatic Non-Small Cell Lung Cancer (NSCLC) , Subtype Adenocarcinoma, Who Have Good Performance Status (PS 0-1) - ELEMENT

Status
Completed
Phase
Study type
Observational
Enrollment
70 (actual)
Sponsor
Hoffmann-La Roche · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This multicenter, observational study will evaluate the efficacy and safety of Tarceva (erlotinib) in participants with locally advanced or metastatic adenocarcinoma non-small cell lung cancer and an ECOG performance status of 0-1. Eligible participants receiving Tarceva according to the Summary of Product Characteristics and local label will be followed for the duration of their treatment.

Conditions

Interventions

TypeNameDescription
DRUGErlotinib 150 mg

Timeline

Start date
2013-05-01
Primary completion
2016-01-01
Completion
2016-01-01
First posted
2013-04-19
Last updated
2017-05-04
Results posted
2017-05-04

Locations

5 sites across 1 country: Serbia

Source: ClinicalTrials.gov record NCT01836133. Inclusion in this directory is not an endorsement.

An Observational Study of Tarceva (Erlotinib) in Participants With Locally Advanced or Metastatic Adenocarcinoma Non-Sma (NCT01836133) · Clinical Trials Directory