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NCT06948981

GT719 Injection for the Treatment of Recurrent/Refractory CD19 Positive Adult B-cell Malignancies

Recruiting now Phase 1, PHASE2 Last updated 16 September 2025
What this trial tests

Phase 1, PHASE2 trial testing GT719 Injection in Hematological Malignancy (Leukemia- Lymphoma) in 46 participants. Currently enrolling.

Timeline
18 April 2025
Primary endpoint
17 April 2028
17 April 2028

Quick facts

Lead sponsorGrit Biotechnology
PhasePhase 1, PHASE2
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment46
Start date18 April 2025
Primary completion17 April 2028
Estimated completion17 April 2028
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Grit Biotechnology — full company profile →

Who can join

Adults 18 to 75, any sex, with Hematological Malignancy (Leukemia- Lymphoma). Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study is a prospective single-arm open-labled phase I/II clinical trial, including dose escalation and expansion phase, aims to evaluate the safety, efficacy, and cellular pharmacokinetics of GT719 Injection in relapsed/refractory CD19 positive adult B-cell non Hodgkin lymphoma (B-NHL) and B-acute lymphoblastic leukemia (B-ALL) patients. A total of 46 subjects (anticipated) will be enrolled in this study.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of GT719 Injection

Trials testing the same drug.

Other recruiting trials for Hematological Malignancy (Leukemia- Lymphoma)

Currently open trials in the same condition.

Other Grit Biotechnology trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06948981.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing