CompletedNot applicableNCT06557967
Official study title

Study on Prevalence and Impact of Brain Metastases on Survival in Lung Cancer by Line of Treatment

Study summary

This study will use real-world data to assess prevalence of brain metastases in metastatic non-small cell lung cancer (mNSCLC) patients and its impact on associated clinical outcomes.

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Key things to know

Main goalNot specified

This describes the study’s primary purpose.

What is being studiedNo drug

The study team can explain what participation involves.

Who it may be forNon-small cell lung cancer (NSCLC) · Metastatic or stage IV

These are broad labels—not an eligibility decision.

Checked against the public recordLast updated Dec 9, 2024 · Source: ClinicalTrials.gov

Is enrollment open?Completed

Ask the study team to confirm whether enrollment is open.

What kind of study?Not applicable

Observational

Where is it offered?1 U.S. location

Locations may change over time.

Who runs it?Daiichi Sankyo

Study sponsor

01
Study overview

What this study is about

Purpose
Not specified
Study type
Observational
Phase
Not applicable
Sponsor
Daiichi Sankyo
Interventions being studied
Other: No drug
02
Explore related studies

How this study is categorized

These labels come from structured fields and exact terms in the public record.

03
Public criteria

Who may be able to participate

The sponsor separates these requirements into two groups. You do not need to interpret them alone—use them to guide a conversation with the study team.

Requirements people may need to meetInclusion criteria

1. Diagnosis of mNSCLC in study period (01/01/2015-06/30/2023) including newly diagnosed at metastatic stage or progression from advanced stage NSCLC 2. Age 18+ years at the time of diagnosis of mNSCLC Additional inclusion criteria for 1st Line of Therapy cohort: 3. Treated with systemic anti-cancer therapy in 1L setting Additional inclusion criteria for 2nd Line of Therapy and 3rd Line of Therapy cohorts: 4. Treated with systemic anti-cancer therapy in 2L setting treated with systemic anti-cancer therapy in 3L setting

Reasons someone may not be able to joinExclusion criteria

1. Evidence of other primary malignancy in the 365-day baseline period immediately prior to the first mNSCLC diagnosis in the study period 2. Evidence of stereotactic radiosurgery (SRS), stereotactic radiation therapy (SRT), or whole brain radiotherapy (WBRT) in the baseline period

Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.

04
Study sites

U.S. locations

  • ConcertAI DatabaseCambridge, Massachusetts

Source and freshness
Processed from ClinicalTrials.gov. Last public update: Dec 9, 2024. Always confirm current availability with the study team.

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