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Brief Title: A Study of MGC026 in Participants With Advanced Solid Tumors
Official Title: A Phase 1/1b First-in-Human, Open Label, Dose Escalation and Cohort Expansion Study of MGC026 in Participants With Advanced Solid Tumors
Study ID: NCT06242470
Brief Summary: The study is designed to understand the safety, tolerability, pharmacokinetics, immunogenicity, and preliminary antitumor activity of MGC026 in participants with relapsed or refractory, unresectable, locally advanced or metastatic solid tumors The study has a dose escalation portion and a cohort expansion portion of the study. Participants will receive MGC026 by intravenous (IV) infusion. The dose of MGC026 will be assigned at the time of enrollment. Participants may receive up to 35 treatments if there are no severe side effects and as long as the cancer does not get worse. Participants will be monitored for side effects, and progression of cancer, have blood samples collected for routing laboratory work, and blood samples collected for research purposes.
Detailed Description:
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
START Midwest, Grand Rapids, Michigan, United States
The University of Texas MD Anderson Cancer Center, Houston, Texas, United States
START Mountain Region, West Valley City, Utah, United States
Name: Denise Casey, MD
Affiliation: MacroGenics
Role: STUDY_DIRECTOR