Overview

A Study of GNC-038, a Tetra-specific Antibody, in Participants With R/R Non-Hodgkin Lymphoma

Status:
Recruiting
Trial end date:
2022-11-01
Target enrollment:
Participant gender:
Summary
In this study, the safety and tolerability of GNC-038 in participants with recurrent or refractory Non-Hodgkin lymphoma 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 future clinical study will also be determined.
Phase:
Phase 1
Details
Lead Sponsor:
Sichuan Baili Pharmaceutical Co., Ltd.
Collaborator:
SystImmune Inc.