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RECRUITING
NCT07312630
EARLY_PHASE1

Clinical Study of LV009 Injection for the Treatment of Relapsed/Refractory CD19-Positive Hematologic and Lymphoid Malignancies

Sponsor: PersonGen BioTherapeutics (Suzhou) Co., Ltd.

View on ClinicalTrials.gov

Summary

Evaluate the safety, pharmacokinetic (PK) characteristics, and pharmacodynamic (PD) characteristics of LV009 injection in subjects with relapsed/refractory CD19-positive hematologic malignancies.

Key Details

Gender

All

Age Range

18 Years - 70 Years

Study Type

INTERVENTIONAL

Enrollment

19

Start Date

2025-09-25

Completion Date

2027-12-12

Last Updated

2025-12-31

Healthy Volunteers

No

Interventions

BIOLOGICAL

LV009 Injection Infusion

A dose escalation was conducted using four fixed doses of LV009 injection solution: 0.3 × 10\^9, 0.6 × 10\^9, 1.2 × 10\^9, and 2.4 × 10\^9 TU.

Locations (1)

PersonGen.Anke Cellular Therapeutice Co., Ltd.

Hefei, Anhui, China