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NCT07126782

The Efficacy and Safety Assessment of Allogeneic γδ T Cells in Patients With MRD-positive AML After Allo-HSCT

Recruiting now EARLY_PHASE1 Last updated 17 August 2025
What this trial tests

EARLY_PHASE1 trial testing Ex-vivo expanded allogeneic γδ T cells in AML (Acute Myelogenous Leukemia) in 10 participants. Currently enrolling.

Timeline
20 July 2025
Primary endpoint
20 December 2027
20 July 2028

Quick facts

Lead sponsorInstitute of Hematology & Blood Diseases Hospital, China
PhaseEARLY_PHASE1
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment10
Start date20 July 2025
Primary completion20 December 2027
Estimated completion20 July 2028
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Institute of Hematology & Blood Diseases Hospital, China

Who can join

18 and older, any sex, with AML (Acute Myelogenous Leukemia) or AML. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to evaluate the efficacy and safety of allogeneic γδ T cells in patients with MRD-positive AML after allo-HSCT.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Ex-vivo expanded allogeneic γδ T cells

Trials testing the same drug.

Other recruiting trials for AML (Acute Myelogenous Leukemia)

Currently open trials in the same condition.

Other Institute of Hematology & Blood Diseases Hospital, China 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/NCT07126782.

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