About this trial
This is a single-arm, open-label, single-center, phase I study. The primary objective is to evaluate the safety of CD7 CAR-T Bridging to allo-HSCT therapy for patients with severe aplastic anemia
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Chinese expert consensus on the diagnosis and treatment of aplastic anemia(2017), Diagnosis of severe aplastic anemia ,1. The degree of bone marrow cell proliferation < 25%, or 25%-50% but residual hematopoietic cells < 30%;2. With pancytopenia (at least two of the following peripheral blood parameters) : (1) absolute neutrophil <0.5×10^9/L; (2) Platelet count< 20×10^9/L; (3) The absolute value of reticulocytes <20×109/L;
Suitable donors (relatives) with allogeneic HSCT indications and at least haploid allogeneic transplantation;
Patients who are not suitable or unwilling to undergo traditional allogeneic hematopoietic stem cell transplantation;
creatinine clearance > 60ml/min; without liver invasion, serum total bilirubin ≤ 1.5 times the upper limit of normal, and serum alanine aminotransferase (ALT) and aspartate aminotransferase (AST) were both ≤ 3 times the upper limit of the normal range. If there is liver invasion, serum erythrambirubin ≤ 3 times the upper limit of normal, and serum ALT and AST are both ≤ 5 times the upper limit of the normal range;
Disqualifiers
Allergy to pre-treatment measures;
Those with acute graft versus host disease (GvHD) or moderate to severe chronic GvHD within 4 weeks before screening; Those who have received systemic drug therapy for GvHD within 4 weeks before the reinfusion;
History of epilepsy or other central nervous system disorders;
Electrocardiogram shows prolonged QT interval, severe heart diseases such as severe arrhythmia in the past;
Trial design
Single group
Treatments tested in this trial
CD7 CAR-T cells injection
DrugCD7 CAR T cells treat patients with severe aplastic anemia
Allogeneic hematopoietic stem cell transplantation
Other interventionIn this study, Allogeneic hematopoietic stem cell transplantation is used as a bridge therapy to CD7 CAR T cells infusion to treat patients with severe aplastic anemia
Treatment groups
Trial outcomes
Primary outcomes
Dose-limiting toxicity (DLT)
Adverse events assessed according to NCI-CTCAE v5.0 criteria
Incidence of treatment-emergent adverse events (TEAEs)
Incidence of treatment-emergent adverse events \[Safety and Tolerability\]
Secondary outcomes
Allogeneic hematopoietic stem cell transplant implantation rate
The proportion of the number of patients who achieved hematopoietic reconstitution to the total number of allogeneic hematopoietic stem cell transplantation patients in the same period.
Time to neutrophil and platelet engraftment
The time for neutrophils and platelets to reach the implantation criteria after stem cell reinfusion
Disease-feesurvival,DFS
The proportion of disease-free patients who survived to the total number of patients who transplanted allogeneic hematopoietic stem cells during the same period.
Overall survival, OS
After transplantation until death from any cause.
Locations
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Sponsors and contacts
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Zhejiang University
Lead sponsor
Yake Biotechnology Ltd.
Collaborator