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Clinical Trials/NL-OMON46049
NL-OMON46049
Completed
Phase 4

A non-interventional biomarker study in patients with NSCLC of adenocarcinoma tumour histology eligible for treatment with Vargatef according to the approved label - Biomarker study in patients with NSCLC

Boehringer Ingelheim0 sites34 target enrollmentTBD

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
lung cancer
Sponsor
Boehringer Ingelheim
Enrollment
34
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Observational invasive

Investigators

Eligibility Criteria

Inclusion Criteria

  • \- Women and men with locally advanced, metastatic or locally recurrent NSCLC with histology of adenocarcinoma
  • \- Vargatef is initiated and administered in accordance with the SPC
  • \- Available fixed and paraffin embedded (FPE) tumour tissue routinely obtained at diagnosis and/or re\-biopsy before the initiation of the first line treatment (either block or slides, minimum of 10 slides and up to 20 slides if possible at 5 um thickness).

Exclusion Criteria

  • \- Any contraindication to Vargatef or docetaxel as specified in their respective labels
  • \- Vargatef initiated from more than 7 days prior to inclusion in this NIS
  • \- Patients participating simultaneously in another NIS or a clinical trial

Outcomes

Primary Outcomes

Not specified

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