T Cell Acute Lymphoblastic Leukemia/Lymphoblastic Lymphoma

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Review clinical trials related to T Cell Acute Lymphoblastic Leukemia/Lymphoblastic Lymphoma. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Autologous Versus Allogeneic Hematopoietic Stem Cell Transplantation for T-Lymphoblastic Leukemia/Lymphoma in First Complete Remission

To evaluate, through a prospective multicenter observational study, autologous or allogeneic hematopoietic stem cell transplantation (Auto-SCT/allo-SCT)as consolidation therapy in subjects with T lymphoblastic leukemia/Lymphoblastic lymphoma(T-ALL/LBL)who have achieved first complete remission (CR). Assess relapse-free survival (RFS), overall survival (OS), cumulative incidence of relapse (CIR), and non-relapse mortality (NRM) among different treatment regimens

Participants needed: 84
Trial details
Age: 14-55Biological sex: AllType: ObservationalSponsor: Shanghai General Hospital, Shanghai Jiao Tong University School of MedicineUpdated: May 13, 2026Duration: 24 Months
Eligibility criteria

Age 14-55 years, no gender restriction [+8]

Malignancies other than acute T-lymphoblastic leukemia, T-cell lymphoma, or T-ly... [+8]

Status: Recruiting

CD7-CAR-T Cells in Pediatric Relapsed/Refractory CD7+ T-ALL/LL

The main purpose of this study is to evaluate the safety, to establish the recommended dose, and to evaluate the antitumor effect of CD7-CART01 in pediatric patients with relapsed or refractory (R/R) T-cell acute lymphoblastic leukemia (T-ALL) or lymphoblastic lymphoma (T-LL).

Participants needed: 26
Trial details
Phase: Phase 1, Phase 2Age: 6-25Biological sex: AllType: InterventionalSponsor: Bambino Gesù Hospital and Research InstituteUpdated: Dec 2, 2025Locations: 1
Eligibility criteria

Patients in 1st or subsequent relapse, after at least one standard frontline che... [+8]

Severe, uncontrolled active intercurrent infections. [+43]

Status: Recruiting

Newly-diagnosed Pediatric T-cell ALL Protocol

This is a prospective, multicenter study conducted within the Chinese Children's Cancer Group (CCCG). The study aims to evaluate whether the addition of three novel agents, dasatinib, venetoclax and homoharringtonine, can improve the minimal residual disease (MRD)-negative remission rate, enhance event-free survival (EFS), and reduce the cumulative incidence of relapse (CIR) in pediatric patients with newly diagnosed T-cell acute lymphoblastic leukemia (T-ALL).

Participants needed: 610
Trial details
Phase: Phase 2, Phase 3Age: 1-18Biological sex: AllType: InterventionalSponsor: Institute of Hematology & Blood Diseases Hospital, ChinaUpdated: Aug 26, 2025Locations: 27
Eligibility criteria

Age older than 1 month to younger than 18 years. [+2]

B-ALL [+10]