MET Non Small Cell Cancer Registry (MOMENT)
This registry is collecting information on people with advanced non-small cell lung cancer (NSCLC) that has a specific genetic change called METex14 skipping alterations. You could join if you have this type of cancer, have signed a consent form, and are starting or already receiving systemic therapy (treatment that affects the whole body). The registry aims to understand how treatments are changing and how well they work over time. Researchers will look at how your tumor responds to treatment (Best Overall Response and Tumor Response according to RECIST 1.1 criteria) and how long people live (Overall Survival) for up to about 4.9 years. This is an observational study, meaning you will receive your usual care, and no specific treatments are being tested.
- Study design
- This is an observational study collecting data from up to 700 participants. It is a disease registry, meaning it gathers information on a specific patient group over time without testing new treatments.
- What's involved
- Not specified in the trial record.
- Compensation
- Not stated in the trial record.
- Follow-up
- Your health information will be collected for up to approximately 4.9 years.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Met Non Small Cell Cancer Registry (MOMENT)
At a glance
Conditions
Where it's being run
79 sites across 20 statesStudy leadership
- Medical Responsible · STUDY_DIRECTOR · Merck Healthcare KGaA, Darmstadt, Germany, an affiliate of Merck KGaA, Darmstadt, Germany
Who to contact
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Do you actually qualify for this trial?
Add a private profile and we'll compare every criterion below against your situation — and tell you which ones are met, uncertain, or excluding.
Inclusion
Exclusion
What this trial measures
- Best Overall Response (BOR)Through study completion, up to approximately 4.9 years
- Tumor Response According to Response Evaluation Criteria in Solid Tumors Version (RECIST) 1.1Up to approximately 4.9 years
- Overall Survival (OS)Through study completion, up to approximately 4.9 years
- Number of Participants with Adverse Events (AEs)Up to approximately 4.9 years
- Number of Participants with Adverse Reactions (ARs)Up to approximately 4.9 years