In this study, the safety and preliminary efficacy of GNC-038 in patients with r relapsed or refractory primary central nervous system lymphoma (PCNSL) and relapsed or refractory secondary central nervous system lymphoma (SCNSL) will be investigated to assess the dose-limiting toxicity (DLT), maximum tolerated dose (MTD) or maximum administered dose (MAD) for MTD is not reached of GNC-038. The recommended dose for phase II (RP2D) clinical study will also be determined.
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Dose limiting toxicity (DLT)
Timeframe: Up to 17 days after the first dose
Maximum tolerated dose (MTD) or maximum administrated dose (MAD)
Timeframe: Up to 17 days after the first dose
Treatment-Emergent Adverse Event (TEAE)
Timeframe: Up to approximately 36 months
The recommended dose for phase II clinical study(RP2D)
Timeframe: Up to 17 days after the first dose