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NCT06720324

CD7-specific CAR-T Cell in the Treatment of CD7-positive Relapsed/Refractory Hematologic Tumors

Recruiting now Phase 1, PHASE2 Last updated 6 December 2024
What this trial tests

Phase 1, PHASE2 trial testing Fludarabine + Cyclophosphamide + CD7-specific CAR-T Cells in Hematologic Malignancy in 80 participants. Currently enrolling.

Timeline
31 December 2024
Primary endpoint
31 December 2027
31 December 2027

Quick facts

Lead sponsorUnion Hospital, Tongji Medical College, Huazhong University of Science and Technology
PhasePhase 1, PHASE2
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment80
Start date31 December 2024
Primary completion31 December 2027
Estimated completion31 December 2027
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

Who can join

Adults 3 to 75, any sex, with Hematologic Malignancy. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study is a single-center, open, prospective single-arm clinical study of patients with CD7 postive relapsed / refractoryhematological tumors to evaluate the safety and efficacy of CD7-specific CAR-T cells in relapsed / refractory hematological tumors while collecting pharmacokinetics and pharmacodynamics indicators of CAR-T cells.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Hematologic Malignancy

Currently open trials in the same condition.

Other Union Hospital, Tongji Medical College, Huazhong University of Science and Technology 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/NCT06720324.

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