Ovarian Cancer Clinical Trial
First-in-human Study of BAY2287411 Injection, a Thorium-227 Labeled Antibody-chelator Conjugate, in Patients With Tumors Known to Express Mesothelin
Summary
The purpose of this study is to evaluate, in patients with tumors known to express the protein mesothelin, the following properties of BAY2287411 injection:
safety (to identify, assess, minimize, and appropriately manage the risks associated to the study drug)
tolerability (the degree to which side effects can be tolerated by your body)
maximum tolerated dose
pharmacokinetics (the effect of your body on the study drug)
anti-tumor activity
recommended dose for further clinical development
Eligibility Criteria
Inclusion Criteria:
Signed informed consent
Male or female subjects ≥ 18 years of age
ECOG PS (Eastern Cooperative Oncology Group Performance Status) of 0 or 1
Patients with advanced malignant epithelioid mesothelioma or advanced recurrent serous ovarian cancer, who have exhausted available therapeutic options; in addition, in the dose expansion part of the study, patients with metastatic pancreatic adenocarcinoma, who have exhausted available therapeutic options
Availability of fresh or archival tumor tissue samples
Adequate bone marrow, liver and renal function, as assessed by pre-defined laboratory requirements (within 28 days before start of study drug treatment)
A negative serum pregnancy test in women of childbearing potential (WOCBP) performed within 7 days before the start of study drug administration. Women and men of reproductive potential must agree to use highly effective methods of contraception, when sexually active.
Exclusion Criteria:
Impaired cardiac function, clinically significant cardiac disease or cardiac arrhythmias
Pericarditis (any CTCAE grade) or pericardial effusion (CTCAE Grade ≥ 2)
Left Ventricular Ejection Fraction (LVEF) < 50% (as measured at screening by echocardiogram).
History of anaphylactic reactions to monoclonal antibody therapy
History of Myelodysplastic syndrome (MDS)/treatment-related acute myeloid leukemia (t-AML) or with features suggestive of MDS/AML
Infections of CTCAE (Common Terminology Criteria for Adverse Events) version 5.0 Grade 2 not responding to therapy or active clinically serious infections of CTCAE Grade >2; known human immunodeficiency virus (HIV) infection; active hepatitis B virus (HBV) or hepatitis C virus (HCV)infection requiring treatment. Patients with chronic HBV or HCV infection are eligible at the investigator's discretion provided that the disease is stable and sufficiently controlled under treatment
Known brain, spinal or meningeal metastases
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There are 7 Locations for this study
Bethesda Maryland, 20892, United States
Houston Texas, 77030, United States
Helsinki , 00290, Finland
Amsterdam , 1066 , Netherlands
Groningen , 9713 , Netherlands
Lund , 221 8, Sweden
Sutton Surrey, SM2 5, United Kingdom
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