About this trial
This is a Phase 1a/1b, first-in-human (FIH), open-label, multi-center dose escalation and expansion study of the safety, pharmacokinetics (PK), pharmacodynamics, and antitumor activity of single-agent CT-95 in subjects with advanced (recurrent, unresectable, or metastatic) cancers associated with MSLN expression.
Eligibility criteria
Qualifiers
ECOG 0 or 1
Subjects with evaluable disease per RECIST 1.1 or mRECIST
Subjects with adequate organ function.
Subjects with advanced cancers associated with mesothelin expression
Disqualifiers
Uncontrolled significant active infection or any medical or other condition that in opinion of the investigator would preclude the subject's participation in the study.
Prior treatment with MSLN-targeted CD3 or chimeric antigen receptor T cell (CAR-T) therapy
Concurrent participation in another investigational clinical trial.
Evidence of leptomeningeal disease
Trial design
Treatments tested in this trial
- CT-95