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Trials / Active Not Recruiting

Active Not RecruitingNCT05192486

A Study of GNC-038, a Tetra-specific Antibody, in Participants With R/R Diffuse Large B-cell Lymphoma (DLBCL)

An Open-Label, Multi-Center, Phase Ib/II Study to Evaluate the Safety, Tolerability and Pharmacokinetic Characteristics of Tetra-specific Antibody GNC-038 in Participants With Recurrent or Refractory Diffuse Large B-cell Lymphoma (DLBCL)

Status
Active Not Recruiting
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
12 (actual)
Sponsor
Sichuan Baili Pharmaceutical Co., Ltd. · Industry
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

In this study, the safety and preliminary efficacy of GNC-038 in participants with recurrent or refractory Diffuse Large B-cell lymphoma (DLBCL) 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.

Conditions

Interventions

TypeNameDescription
DRUGGNC-038Administration by intravenous infusion

Timeline

Start date
2022-08-10
Primary completion
2025-12-01
Completion
2025-12-01
First posted
2022-01-14
Last updated
2025-09-26

Locations

4 sites across 1 country: China

Source: ClinicalTrials.gov record NCT05192486. Inclusion in this directory is not an endorsement.