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Study details
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Gene Therapy for CD19-Positive Hematologic Malignancies (SENTRY-CD19)

Vironexis Biotherapeutics Inc.
NCT IDNCT06533579ClinicalTrials.gov data as of Apr 2026
Phase

Phase 1/2

Target enrollment

32

Study length

about 6.3 years

Ages

13–90

Locations

9 sites in CA, CO, NC +5

What this study is about

This trial is testing a treatment called VNX-101 in people with relapsed or refractory CD19-positive blood cancers. The goal is to see if VNX-101 is safe and effective.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Take Dose Level 1, VNX-101
  • 2.Take Dose Level 2, VNX-101
  • 3.Take Dose Level 3, VNX-101
  • +1 more

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Standard

How treatment is administered

Treatment Assignment
All receive treatment

Everyone gets the investigational treatment.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Endpoints

Primary: Treatment emergent adverse events (TEAEs) and treatment-emergent serious events (TESAEs)

Secondary: Change from baseline in B-cell counts, Proportion/duration of subjects achieving response, progression free survival, and disease free survival.

Body systems

Oncology