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Clinical Trial Summary

The primary objectives of this study are: - To investigate the safety and tolerability, and to define the recommended Phase 2 dose and schedule (RP2DS) for magrolimab in combination with rituximab and for magrolimab in combination with rituximab, gemcitabine, and oxaliplatin (R-GemOx). - To evaluate the efficacy of magrolimab in combination with rituximab in participants with indolent lymphoma and diffuse large B-cell lymphoma (DLBCL) and to evaluate the efficacy of magrolimab in combination with R-GemOx in autologous stem cell transplant (ASCT) ineligible DLBCL participants.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02953509
Study type Interventional
Source Gilead Sciences
Contact
Status Terminated
Phase Phase 1/Phase 2
Start date November 21, 2016
Completion date March 25, 2024

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