Study identifier:D7900C00001
ClinicalTrials.gov identifier:NCT03489525
EudraCT identifier:N/A
CTIS identifier:N/A
A Phase 1, Open-label Study to Evaluate the Safety, Pharmacokinetics, Immunogenicity, and Preliminary Efficacy of MEDI2228 in Subjects with Relapsed/Refractory Multiple Myeloma
relapsed/refractory multiple myeloma
Phase 1
No
-
All
107
Interventional
18 Years - 101 Years
Allocation: Non-randomized
Endpoint Classification: -
Intervention Model: Sequential Assignment
Masking: -
Primary Purpose: Treatment
Verified 01 Apr 2023 by MedImmune, LLC
MedImmune, LLC
-
No locations available
Arms | Assigned Interventions |
---|---|
Experimental: Dose Escalation, MEDI2228, ADC Single agent MEDI2228, ADC (antibody drug conjugate) will be administered to adult subjects with relapsed/refractory (R/R) multiple myeloma (MM). | Biological/Vaccine: Dose Escalation, MEDI2228, ADC (antibody drug conjugate) Single agent MEDI2228 will be administered to adult subjects with R/R MM. The study aims to evaluate up to 9 planned, sequentially ascending main dose levels |
Experimental: Dose Expansion, MEDI2228, ADC Single agent MEDI2228, ADC (antibody drug conjugate) will be administered to adult subjects with R/R MM in the dose-expansion cohort at the dose selected for evaluation in the dose-expansion phase. | Biological/Vaccine: Dose Expansion, MEDI2228, ADC (antibody drug conjugate) Adult subjects with R/R MM with measurable disease will be enrolled in the dose-expansion cohort at the dose selected for evaluation in the dose-expansion phase. |