A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of YK012

PHASE1RecruitingINTERVENTIONAL
Enrollment

48

Participants

Timeline

Start Date

May 9, 2023

Primary Completion Date

June 30, 2026

Study Completion Date

December 31, 2026

Conditions
Relapsed or Refractory B-Cell Non-Hodgkin Lymphoma
Interventions
DRUG

YK012

YK012 is a bispecific antibody targeting CD19 on B cells and CD3 on T cells leading to T cell-mediated cytotoxicity of malignant B cells

Trial Locations (1)

100021

RECRUITING

Cancer Institute and Hospital, Chinese Academy of Medical Sciences, Beijing

Sponsors
All Listed Sponsors
lead

Excyte Biopharma Ltd

INDUSTRY