A Study of Investigational Agents in Participants With Previously Treated Stage IV Nonsquamous Non-small Cell Lung Cancer (NSCLC) (MK-3475-01H/KEYMAKER-U01)
Eligible age
18+ yrs
Accepts
All genders
Locations
3 states
Healthy volunteers
No
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About this study
Researchers are looking for new ways to treat metastatic nonsquamous non-small cell lung cancer (NSCLC) that has been treated before. Metastatic means the cancer has spread to other parts of the body. Nonsquamous means the cancer did not start in squamous cells, which are flat cells that line the inside of the lungs. Standard treatment (usual treatment) for NSCLC is surgery, then immunotherapy with or without chemotherapy after surgery. Immunotherapy is a treatment that helps the immune system fight cancer. Chemotherapy is a medicine that works to destroy cancer cells or stop them from growing. However, standard treatment may not work or may stop working for some people. Researchers want to know if 2 antibody drug conjugates (ADCs) can help treat metastatic nonsquamous NSCLC that did not respond (get smaller or go away) to treatment. An ADC attaches to specific targets on cancers cells and delivers treatment to destroy those cells. Researchers will compare 2 different ADCs (the study treatments) to chemotherapy in this study. The goals of this study are to learn: * About the safety of the study treatments and if people tolerate them * How many people have the cancer respond to the study treatments
Sponsor: Merck Sharp & Dohme LLC
You may qualify if…
- ✓ The main inclusion criteria include but are not limited to the following:
- ✓ Histologically or cytologically confirmed diagnosis of Stage IV nonsquamous non-small cell lung cancer (NSCLC)
- ✓ Documented disease progression per RECIST 1.1 after receiving an anti-programmed cell death 1 protein (PD-1)/programmed cell death ligand 1 (PD-L1) treatment and platinum-based chemotherapy
- ✓ Confirmation per local test report that epidermal growth factor receptor negative (EGFR-), anaplastic lymphoma kinase negative (ALK-), c ros oncogene 1 negative (ROS1-), or other directed therapy is not indicated as primary therapy
- ✓ Measurable disease per RECIST 1.1 as assessed by investigator and verified by BICR
- ✓ Life expectancy of at least 3 months
- ✓ An Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 1 assessed within 7 days before randomization
- ✓ Is an individual of any sex/gender who is at least 18 years of age at the time of providing the informed consent
You may not qualify if…
- ✕ The main exclusion criteria include but are not limited to the following:
- ✕ Diagnosis of small cell lung cancer or, for mixed tumors, presence of small cell elements
- ✕ Received radiation therapy to the lung
- ✕ Has uncontrolled or significant cardiovascular disorder prior to randomization
- ✕ Has clinically severe pulmonary compromise resulting from intercurrent pulmonary illnesses
- ✕ Participants who have adverse events (AEs) (other than alopecia) due to previous anticancer therapies must have recovered to ≤Grade 1 or baseline
- ✕ Has known severe hypersensitivity (≥Grade 3) to study intervention and/or any of its excipients
- ✕ Has clinically significant corneal disease
Where it's recruiting
Source: ClinicalTrials.gov · NCT06780085 · last updated 2026-08-25