Viewing Study NCT06219356


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Ignite Modification Date: 2025-12-25 @ 9:27 PM
Study NCT ID: NCT06219356
Status: RECRUITING
Last Update Posted: 2025-08-19
First Post: 2023-12-22
Is NOT Gene Therapy: False
Has Adverse Events: False

Brief Title: A Study of GLB-002 in Patients With Relapsed or Refractory Non-Hodgkin Lymphomas
Sponsor: Hangzhou GluBio Pharmaceutical Co., Ltd.
Organization:

Study Overview

Official Title: A Phase 1 Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics and Preliminary Efficacy of GLB-002 in Patients With Relapsed or Refractory Non-Hodgkin Lymphomas (R/R NHL)
Status: RECRUITING
Status Verified Date: 2025-06
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Study GLB-002-01 is a first-in-human (FIH), phase 1, open-label, dose escalation and expansion clinical study, the purpose of this study is to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD) and preliminary efficacy of GLB-002 monotherapy in participants with relapsed or refractory Non-Hodgkin lymphomas (R/R NHL).
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: