A Study of MGC018 in Combination With MGD019 in Participants With Advanced Solid Tumors

Inclusion Criteria:

1. Ability to provide and document informed consent and willing and able to comply with all study procedures.
Participants diagnosed with advanced solid tumors including metastatic castration-resistant prostate cancer, melanoma, pancreatic cancer, hepatocellular carcinoma, ovarian cancer and renal cell carcinoma.
Participants have received approved therapies according to their diagnosis.
Participants must have an available tumor tissue sample. A fresh tumor biopsy may be performed if no archival sample is available.
Eastern Cooperative Oncology Group performance status of less than or equal to 2.
Life expectancy of at least 12 weeks.
Evidence of measurable tumor for evaluation
Acceptable end organ function according to laboratory results.
Patients must agree to use highly-effective contraception during the study, and not donate sperm or ova.

Exclusion Criteria:

Any underlying medical or psychiatric condition impairing participant's ability to receive, tolerate, or comply with the planned treatment or study procedures.
Another malignancy that required treatment within the past 2 years. Participants who have had curative therapy for non-melanomatous skin cancer, localized prostate cancer (Gleason score < 6), or carcinoma in situ are eligible for the study.
Active viral, bacterial, or fungal infection requiring systemic treatment within 1 week of initiation of study drug. Participants are eligible after SARS CoV 2-related symptoms have fully recovered for ≥ 72 hours.
History of immunodeficiency. Participants with HIV are eligible if they have a CD4+ count ≥ 300/µL, undetectable viral load, and maintained on antiretroviral therapy with minimal drug-drug interactions or overlapping toxicity of the antiretroviral therapy study treatments.
Prior autologous/allogeneic stem cell or tissue/solid organ transplant
Prior treatment with MGD009, enoblituzumab, or other B7-H3 targeted agents for cancer.
Clinically significant cardiovascular disease, lung compromise, venous insufficiency, or gastrointestinal disorders.
Participants with greater than Grade 1 peripheral neuropathy.
Participants who have a history of severe adverse events (AEs) from immune checkpoint inhibitors (anti-PD-1, anti-PD-L1, or CTLA-4 inhibitors). All other AEs from prior immune checkpoint inhibitors must be resolved to Grade 1 or less.
Pleural effusion or ascites. Trace pleural or peritoneal fluid is not exclusionary.