This study is a Phase 1 dose-finding and dose-confirmation study to evaluate the safety and antitumor activity of UB-VV500. The study will enroll patients with relapsed/refractory multiple myeloma.
Inclusion Criteria:
Exclusion Criteria:
jacob.garcia@umoja-biopharma.com425-873-8331
A single dose of UB-VV500 will be administered.
A single dose of UB-VV500 will be administered followed by treatment with rapamycin.
erin.mullane@umoja-biopharma.com
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