700 Participants Needed

Registry for Lung Cancer

Recruiting at 105 trial locations
CC
UM
Overseen ByUS Medical Information
Age: Any Age
Sex: Any
Trial Phase: Academic
Sponsor: EMD Serono Research & Development Institute, Inc.
Must be taking: Systemic therapy
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial aims to gather information on the effectiveness of treatments for non-small cell lung cancer (NSCLC) over time. It focuses on patients with a specific genetic change called METex14, which influences cancer growth. The study will monitor the efficacy and safety of different treatments for these patients. Individuals with advanced NSCLC who have this genetic change and are receiving systemic therapy (such as chemotherapy) might be suitable candidates for this trial.

As a Phase 3 trial, this study represents the final step before FDA approval, providing access to potentially effective treatments.

Why are researchers excited about this trial?

Researchers are excited about the Met Non Small Cell Cancer Registry because it aims to gather comprehensive data that could lead to more personalized treatments for metastatic non-small cell lung cancer (NSCLC). Unlike current treatments, which often follow a one-size-fits-all approach, this registry seeks to understand the diverse responses patients have to existing therapies. By analyzing genetic and clinical information, the project hopes to uncover new insights and tailor treatments to individual patient profiles, potentially improving outcomes and reducing side effects. This approach represents a shift towards precision medicine, where therapy is customized based on the unique characteristics of each patient’s cancer.

Who Is on the Research Team?

MR

Medical Responsible

Principal Investigator

Merck Healthcare KGaA, Darmstadt, Germany, an affiliate of Merck KGaA, Darmstadt, Germany

Are You a Good Fit for This Trial?

Inclusion Criteria

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
Participants who signed ICF

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Data Collection

Collection of demographic, clinical characteristics, treatment patterns, and outcomes data for NSCLC patients

Ongoing

Follow-up

Participants are monitored for safety and effectiveness after treatment

Long-term

What Are the Treatments Tested in This Trial?

Find a Clinic Near You

Who Is Running the Clinical Trial?

EMD Serono Research & Development Institute, Inc.

Lead Sponsor

Trials
86
Recruited
22,700+

Miguel Fernández Alcalde

EMD Serono Research & Development Institute, Inc.

Chief Executive Officer

Bachelor’s Degree in Pharmacy from the University Complutense in Madrid, MBA from the University of Alcalá de Henares, Master’s Degree in Management from IESE Business School

Danny Bar-Zohar

EMD Serono Research & Development Institute, Inc.

Chief Medical Officer since 2022

MD

Merck KGaA, Darmstadt, Germany

Industry Sponsor

Trials
449
Recruited
122,000+
Danny Bar-Zohar profile image

Danny Bar-Zohar

Merck KGaA, Darmstadt, Germany

Chief Medical Officer since 2022

MD

Belén Garijo profile image

Belén Garijo

Merck KGaA, Darmstadt, Germany

Chief Executive Officer since 2021

MD

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