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Clinical Trial Summary

The objective of this study was to evaluate the safety and efficacy of IMM0306 in combination with lenalidomide in patients with relapsed/refractory CD20-positive B-cell non-Hodgkin lymphoma.


Clinical Trial Description

Main study purpose: To assess the safety and tolerability of IMM0306 in combination with lenalidomide to determine the maximum tolerated dose (MTD) (if available) and the recommended Phase 2 dose (RP2D). Secondary study purpose 1. To assess the antitumor efficacy of IMM0306 in combination with lenalidomide. 2. To assess the immunogenicity of IMM0306 in combination with lenalidomide. 3. To evaluate the pharmacokinetic (PK) profile of IMM0306 in combination with lenalidomide. Exploratory study purpose: 1. Explore the correlation between exposure to IMM0306 and efficacy and safety (data permitting). 2. Explore the correlation of biomarkers with safety. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05771883
Study type Interventional
Source ImmuneOnco Biopharmaceuticals (Shanghai) Inc.
Contact jinhua zhou
Phone 02138016387
Email jinhua.zhou@immuneonco.com
Status Not yet recruiting
Phase Phase 1/Phase 2
Start date May 2023
Completion date November 2025

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