RE002 T Cell Injection for the Treatment of KRAS G12D Mutated Solid Tumors

PHASE1Not yet recruitingINTERVENTIONAL
Enrollment

30

Participants

Timeline

Start Date

August 1, 2024

Primary Completion Date

April 1, 2026

Study Completion Date

April 1, 2027

Conditions
KRAS G12DT Cell Therapy
Interventions
BIOLOGICAL

RE002 T cell

All subjects who met the entry and exit criteria and signed the informed consent form were observed in hospital at the beginning of lymphocyte clearance chemotherapy, with the dosage of cyclophosphamide (600-800mg/m2/days,-5,-4 days) and fludarabine (25-30mg/m2/days,-5,-4,-3 days), at least two days after the completion of lymphocyte clearance chemotherapy.

Trial Locations (1)

450008

Henan Cancer Hospital, Zhengzhou

All Listed Sponsors
lead

Henan Cancer Hospital

OTHER_GOV

NCT06546150 - RE002 T Cell Injection for the Treatment of KRAS G12D Mutated Solid Tumors | Biotech Hunter | Biotech Hunter