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Clinical Trial Summary

To explore the safety and efficacy of GNC-038 in relapsed or refractory NK/T cell lymphoma, vascular immunomother T cell lymphoma, and other relapsed or refractory NHL, and to determine MTD, MAD, DLT, and RP2D of GNC-038, as well as its pharmacokinetic characteristics and immunogenicity.


Clinical Trial Description

Phase Ib: To explore the safety and preliminary effectiveness of GNC-038 under the administration mode of "intravenous infusion for 2h to 4h, once a week (IV, QW), 2 weeks as one cycle", and to determine MTD, MAD, DLT and RP2D of GNC-038. The pharmacokinetic characteristics and immunogenicity of GNC-038 will be evaluated. Phase II: To explore the efficacy, safety and tolerability, pharmacokinetic characteristics and immunogenicity of GNC-038. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05627856
Study type Interventional
Source Sichuan Baili Pharmaceutical Co., Ltd.
Contact Hai Zhu, PHD
Phone +8613980051002
Email zhuhai@baili-pharm.com
Status Recruiting
Phase Phase 1/Phase 2
Start date February 21, 2023
Completion date February 2025

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