Safety and Efficacy of PRG-2302 for Refractory or Relapsed B-cell Acute Lymphoblastic Leukemia Disease.

A Clinical Study on the Safety and Effectiveness of CD19/CD22 Chimeric Antigen Receptor T Cells in the Treatment of Refractory or Relapsed B-cell Acute Lymphoblastic Leukemia Disease.

Trial Details

NCT ID
NCT06659653
Phase
EARLY_PHASE1
Sponsor
Tan Jie
Status
RECRUITING
Cancer Type
Leukemia
Interventions
  • PRG2302
Locations (sample)
  • Jinzhou, Hubei, China

Key Eligibility Criteria

  • Age ≥18 years old, not over 70 years old (including 70 years old);
  • Meet the following diagnostic criteria for recurrent or refractory B-ALL:
  • A clear diagnosis of B-cell acute lymphoblastic leukemia with any of the following conditions Patients:
  • recurrent: recurrence within 12 months after the first remission after standard treatment;

For full eligibility, visit ClinicalTrials.gov.

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