Last reviewed · How we verify

NCT06659653

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

Recruiting now EARLY_PHASE1 Last updated 26 October 2024
What this trial tests

EARLY_PHASE1 trial testing PRG2302 in Acute Lymphoblastic Leukemia in 18 participants. Currently enrolling.

Timeline
24 May 2024
Primary endpoint
31 March 2027
31 March 2028

Quick facts

Lead sponsorTan Jie
PhaseEARLY_PHASE1
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment18
Start date24 May 2024
Primary completion31 March 2027
Estimated completion31 March 2028
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Tan Jie — full company profile →

Who can join

Adults 18 to 70, any sex, with Acute Lymphoblastic Leukemia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

Verify or expand the search:

Other recruiting trials for Acute Lymphoblastic Leukemia

Currently open trials in the same condition.

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/NCT06659653.

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