Ovarian Cancer Clinical Trial
A Study of MGC018 in Combination With MGD019 in Participants With Advanced Solid Tumors
Study CP-MGC018-02 is a study of MGC018 in combination with lorigerlimab. The study is designed to characterize safety, tolerability, pharmacokinetics (PK), immunogenicity, pharmacodynamics, and preliminary antitumor activity. Participants with relapsed or refractory, unresectable, locally advanced or metastatic solid tumors including mCRPC, melanoma, pancreatic cancer, hepatocellular carcinoma (HCC), ovarian cancer, and renal cell carcinoma (RCC) will be enrolled.
MGC018 and lorigerlimab are administered separately on Day 1 of every 4-week (28-day) cycle at the assigned dose for each cohort. Participants who do not meet criteria for study drug discontinuation may receive study drugs for up to a total of 35 cycles (approximately 2 years).
Tumor assessments are performed every 8 weeks for the initial 6 months on study drugs, then every 12 weeks (± 21 days) until progressive disease (PD).
Participants will be followed for safety throughout the study. .
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.
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.
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There are 7 Locations for this study
Los Angeles California, 90095, United States
Sarasota Florida, 34232, United States
Baltimore Maryland, 21287, United States
Huntersville North Carolina, 28078, United States
Oklahoma City Oklahoma, 73104, United States
Pittsburgh Pennsylvania, 15232, United States
Charlottesville Virginia, 22908, United States
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