Non-hodgkin's Lymphoma Clinical Trial
Official title:
A Multi-center, Randomized, Double-blind, Parallel Control Clinical Trial to Assess the Similarity of the Safety and Pharmacokinetics of TQB2303 in Combination With Rituximab to Patients With AggressiveCD20 Positive Non-Hodgkin's Lymphoma
Primary Outcome Measures:
Area under the curve (AUC) forTQB2303 and rituximab concentrations [ Time Frame: 85 days ]
Secondary Outcome Measures:
The Maximum Concentration (Cmax) of the TQB2303 and rituximab [ Time Frame: 85 days ] The
area under the plasma concentration-time curve from 0 to inf (infinite) time (AUC0-∞); The
time to reach the maximum plasma concentration after treatment (Tmax) Total clearance (CL);
Elimination of half-life (t1 / 2); Apparent distribution volume (Vd).
n/a
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