Met Non Small Cell Cancer Registry (MOMENT)

ConditionCancer
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorEMD Serono Research & Development Institute, Inc.

About this trial

The purpose of this multi-national disease registry is to collect prospectively (with longitudinal follow-up) high-quality, standardized, and contemporaneous data to capture changes in the non-small cell lung cancer (NSCLC) treatment landscape and outcomes over time.

The registry will capture data on participants; demographic, clinical characteristics (including biomarker data), treatment patterns, and effectiveness and safety outcomes for advanced NSCLC with mesenchymal-epithelial transition exon 14(METex14) participants treated with systemic therapy.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Participants who signed ICF

Participants with advanced stage (stages IIIB-IV) NSCLC (all histologies) and Confirmed METex14 skipping alterations (by valid assay)

Participants who are starting or are already being treated with systemic therapy

Disqualifiers

Participants who are enrolled in a clinical trial

Trial population

Participants with advanced stage (stages IIIB-IV) NSCLC and confirmed METex14 skipping alterations who are initiating or already treated with a systemic therapy will be included.

Trial design

Design model

Other

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

700 Participants
are grouped into 1 trial group
Group A: Advanced Non-small Cell Lung Cancer with METex14 skipping alterations

Trial outcomes

Primary outcomes

1

Best Overall Response (BOR)

Time frame
Through study completion, up to approximately 4.9 years
2

Tumor Response According to Response Evaluation Criteria in Solid Tumors Version (RECIST) 1.1

Time frame
Up to approximately 4.9 years
3

Overall Survival (OS)

Time frame
Through study completion, up to approximately 4.9 years
4

Number of Participants with Adverse Events (AEs)

Time frame
Up to approximately 4.9 years

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

EMD Serono Research & Development Institute, Inc.

Lead sponsor

Merck KGaA, Darmstadt, Germany

Collaborator