A Study of MORAb-202 in Participants With Previously Treated Metastatic Non-Small Cell Lung Cancer (NSCLC) Adenocarcinoma (AC)
The aim of this study is to characterize the safety and tolerability of MORAb-202, and to assess the objective response rate in participants with previously treated, metastatic NSCLC AC.
Checked against the public recordLast updated Sep 4, 2025 · Source: ClinicalTrials.gov
What this study is about
- Purpose
- Treatment
- Study type
- Interventional
- Phase
- Phase 2
- Sponsor
- Bristol-Myers Squibb
- Interventions being studied
- Drug: MORAb-202
How this study is categorized
These labels come from structured fields and exact terms in the public record.
Who may be able to participate
Inclusion Criteria: * Histologically or cytologically documented metastatic NSCLC AC (as defined by the 8th International Association for the Study of Lung Cancer Classification). * Measurable target disease assessed by the investigator according to RECIST 1.1. * Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0 or 1 Exclusion Criteria: * NSCLC histologies other than AC (ie, squamous cell carcinoma, large cell carcinoma). * Significant third-space fluid retention (eg, ascites or pleural effusion) that requires repeated drainage. * Prior pneumonectomy. Prior lobectomy and segmentectomy are allowed \> 12 months before treatment. * Recent chest radiotherapy. Participants with chest or chest wall radiation may be permitted if chest radiation is documented \> 6 months before starting study treatment. Other protocol-defined inclusion/exclusion criteria apply.
Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.
U.S. locations
- Local Institution - 0007Orange, California
- Local Institution - 0035Lone Tree, Colorado
- Local Institution - 0043Clermont, Florida
- Local Institution - 0010Orange City, Florida
- Local Institution - 0001Marietta, Georgia
- Local Institution - 0005Louisville, Kentucky
- Local Institution - 0044Silver Spring, Maryland
- Henry Ford HospitalDetroit, Michigan
- Local Institution - 0002Kansas City, Missouri
- Local Institution - 0011Charlotte, North Carolina
- Local Institution - 0034Arlington, Texas
- Local Institution - 0045Flower Mound, Texas
Source and freshness
Processed from ClinicalTrials.gov. Last public update: Sep 4, 2025. Always confirm current availability with the study team.