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Observational Study on the Management of Patients With Non Small Cell Lung Cancer Adenocarcinoma

Observational Study on the Management of Patients With Non Small Cell Lung Cancer (NSCLC) Adenocarcinoma Tested for the Activating Mutation of Epidermal Growth Factor Receptor Tyrosine Kinase (EGFR TK)

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01167972
Acronym
MUTACT
Enrollment
2000
Registered
2010-07-22
Start date
2010-09-30
Completion date
2012-09-30
Last updated
2012-09-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Non Small Cell Lung Cancer

Keywords

M + mutation, Non Small Cell Lung Cancer adenocarcinoma, To determine the proportion of patients with M + mutation status among patients with NSCLC adenocarcinoma

Brief summary

The main objective of the study is to determine the proportion of patients with M + mutation status among patients with Non Small Cell Lung Cancer adenocarcinoma.

Detailed description

MSD

Interventions

None listed

Sponsors

AstraZeneca
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patient with lung cancer (Non Small Cell Lung Cancer adenocarcinoma) * Patient for whom a search for the mutational status of EGFR (EGFR-M +, M- or Mx) has been done or is being analyzed

Exclusion criteria

* Assessment of mutational status of EGFR is not done

Design outcomes

Primary

MeasureTime frame
The main objective of the study is to determine the proportion of patients with M + mutation status among patients with NSCLC adenocarcinomaAt baseline

Secondary

MeasureTime frame
Describe the therapeutic management according to the mutational status (EGFR M +, EGFR M- and Mx).12 months / At each visit
Describe the therapeutic management of patients with EGFR M +.12 months / At each visit
Describe the clinical course of patients EGFR-M +, treated for first-line treatment, and then 2nd line treatment, until 31-AUG-201212 months / At each visit

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026