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

Recruiting Early Phase 1 Interventional Study
Non-Hodgkin Lymphoma (NHL) Acute Lymphoblastic Leukemia (ALL), Adult
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 – 70
Sex
Any
Trial phase
Early Phase 1
Study type
Interventional
Purpose
Treatment
Participants needed
19 (estimated)
Sponsor
PersonGen BioTherapeutics (Suzhou) Co., Ltd. · Industry
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About This Trial

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

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Age 18 to 70 years old (inclusive of both age limits), no gender restrictions, no racial restrictions * Expected survival time exceeds 12 weeks * ECOG performance status 0-2 * Meets the NCCN guidelines' criteria for recurrence/refractory disease and is diagnosed with CD19-posi…
Contacts

Xingbing Wang, Doctor

+86-13856007984

wangxingbing@ustc.edu.cn

CONTACT