PROCLAIM: CX-072-002: Study of PD-L1 Probody Therapeutic CX-072 in Combination With Other Anticancer Therapy in Adults With Solid Tumors

Inclusion Criteria:

At least 18 years of age
Measurable disease as defined by RECIST v1.1
Eastern Cooperative Oncology Group (ECOG) performance status of ≤1
Agree to provide tumor tissue and blood samples for biomarker assessment

Exclusion Criteria:

Treatment with cytotoxic chemotherapy, biologic agents, radiation, immunotherapy, or any investigational agent within 28 days prior to the first dose of study treatment.
Prior therapy with a chimeric antigen receptor T cell-containing regimen
History of active autoimmune disease(s) including but not limited to inflammatory bowel diseases, rheumatoid arthritis, autoimmune thyroiditis, autoimmune hepatitis, systemic sclerosis, systemic lupus erythematosus, autoimmune vasculitis, autoimmune neuropathies, type 1 insulin-dependent diabetes mellitus
History of myocarditis regardless of the cause
History of intolerance to prior checkpoint inhibitor therapy defined as the need to discontinue treatment due to an irAE
History of any syndrome or medical condition that required treatment with systemic steroids (≥10 mg daily prednisone equivalents) or immunosuppressive medications.
History of severe allergic or anaphylactic reactions to human mAb therapy or known hypersensitivity to any Probody therapeutic