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.
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