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A Study of ZW191 in Participants With Solid Tumors
Trial Status: active
The purpose of this study is to find out if ZW191 is safe and can treat participants with
advanced cancers, including ovarian, endometrial, and non-small cell lung cancers.
Inclusion Criteria
Pathologically or cytologically confirmed diagnosis of cancers with evidence of locally advanced (unresectable), recurrent and/or metastatic disease.
Measurable disease per RECIST v1.1.
Eastern Cooperative Oncology Group (ECOG) Performance Status score of 0 or 1.
Adequate cardiac function: Cardiac left ventricular function, as defined by left ventricular ejection fraction (LVEF) ≥ 50% as determined by either echocardiogram (ECHO) or multigated acquisition scan (MUGA).
Other adequate organ function.
Exclusion Criteria
Known additional malignancy that is progressing or requires active treatment or may interfere with study endpoints.
Has received prior Topoisomerase I inhibitor(TOPO1i) antibody drug conjugate treatment, regardless of washout period.
Acute or chronic uncontrolled renal disease, pancreatitis, or liver disease.
Severe chronic or active infections (including known active SARS-CoV-2 infection) requiring systemic therapy, including antibacterial, antifungal, or antiviral therapy.
Additional locations may be listed on ClinicalTrials.gov for NCT06555744.
Locations matching your search criteria
United States
Connecticut
New Haven
Yale University
Status: Active
Name Not Available
Trumbull
Smilow Cancer Hospital Care Center-Trumbull
Status: Active
Name Not Available
Ohio
Columbus
Ohio State University Comprehensive Cancer Center
Status: Active
Name Not Available
Oklahoma
Oklahoma City
University of Oklahoma Health Sciences Center
Status: Active
Name Not Available
Part 1 of the study will evaluate the safety and tolerability of ZW191. Part 2 of the
study will further evaluate safety and explore the potential anti-tumor activity of