First Patient Infused in Joint Humanigen/Kite, A Gilead Company Clinical Study

On June 30, 2020 Humanigen, Inc., (HGEN) ("Humanigen"), a clinical stage biopharmaceutical company focused on preventing and treating cytokine release syndrome (CRS) with lenzilumab, the company’s proprietary Humaneered anti-human granulocyte macrophage-colony stimulating factor (GM-CSF) monoclonal antibody, reported that the first patient has been infused in the ZUMA-19 study, which is being conducted in collaboration with Kite, A Gilead Company (Press release, Humanigen, JUN 30, 2020, View Source [SID1234561585]). Details of the ZUMA-19 study can be found at www.clinicaltrials.gov/ct2/show/NCT04314843.

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"We are excited to see this clinical collaboration move forward as we seek to understand the potential benefit of lenzilumab being administered with CAR T therapy in patients with relapsed or refractory large B-cell lymphoma," said Cameron Durrant, MD, chief executive officer of Humanigen.