Hyderabad:The interim results of clinical trial of I-Mab-discovered TJM2, to evaluate the therapeutic role of anti granulocyte-macrophage colony stimulating factor (GM-CSF) antibody in severe COVID-19 patients, suggest that it is potential enough to address the complications among the severe and critically-ill patients and ultimately save lives.
I-Mab, clinical-stage bio pharmaceutical company committed to the discovery, development and commercialization of novel biologics, followed a rigorous and robust clinical trial protocol, the first among similar anti-GM-CSF antibody studies globally, to ensure robustness of the study conclusion and data integrity.
The announcement was made by the data monitoring committee (DMC), who reviewed the part 1 of the study to assess patient's safety and overall conduct of the study.
Following which, after comprehensive review and analysis, the DMC concluded that I-Mab can commence the Part 2 of the study as planned, indicating TJM2 is safe and well-tolerated in the severe COVID-19 patients.
"Part 2 of the study with a similar design to Part 1 will target the same patient population and is expected to be initiated shortly. It will evaluate the efficacy, safety and cytokine levels following a single dose of 6mg/kg TJM2or placebo in 120 patients with severe COVID-19," informed the committee.
Additionally, the DMC also endorsed protocol changes, including broadening the inclusion criteria and dosing all patients at 6 mg/kg of TJM2 or placebo.