Therefore, a clinical study in NHL patients to compare the standard, approved, subcutaneously (SC) administered, WB plerixafor dosing regimen of 0.24 mg/kg with a fixed-dose (FD) regimen of 20 mg/kg SC in patients with NHL weighing ≤70 kg after both sets of patients had received G-CSF for 4 days was conducted. The gene discussed is CSF3; the disease is non-Hodgkin lymphoma.