Clinical trial · Interventional
Safety and Efficacy of OC-1 Therapy in Patients With R/R T-ALL/LL
Safety and Efficacy of hCD1a-CAR T (OC-1) Therapy, in Patients With Relapsed/Refractory (R/R) T-cell Acute Lymphoblastic Leukemia/Lymphoma (T-ALL/LL
NCT05679895CI-TRIAL-00105262CARxALLrecruitingPhase 1ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
First in humans, exploratory, open-label, single-arm, multicentre, non-competitive, dose escalation study to assess the safety and efficacy of CD1a-CAR T therapy in patients with relapsed/refractory (R/R) T-cell acute lymphoblastic leukemia/lymphoma (T-ALL/LL)
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Lymphoblastic T-Cell Lymphoma | — | UNRESOLVED | — |
| T-cell Acute Lymphoblastic Leukemia | T Acute Lymphoblastic Leukemia | CURATED_BROADER | 0.80 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| CD1a-CAR T | Biological | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Experimental: CD1a-CAR T
- description
- CD1a CAR T cells transduced with a lentiviral vector to express CD1a chimeric receptor domain on T cells administered with a dose-escalation approach.
- interventionNames
- Biological: CD1a-CAR T
Primary outcomes (7)
- measure
- Number of adverse events grade III-IV
- timeFrame
- 1 year particularly the first 28 days after infusion
- description
- Number of adverse events grade III-IV using common toxicity criteria (CTC)
- measure
- Incidence of severe Cytokine release syndrome (CRS) and Immune effector cell-associated neurotoxicity syndrome (ICANS)
- timeFrame
- 1 year particularly the first 28 days after infusion
- description
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 2 Years
Show eligibility criteria text
Inclusion Criteria 1. Children older than 2 years or adults, male and female in both groups. 2. Patients CD1a antigen blast expression ≥20% at inclusion, either immunophenotypically (flow cytometry) or histologically confirmed. 3. R/R CD1a-positive T-ALL/LL patients defined as: * Failure to achieve morphological complete remission (\> 5% bone marrow blasts) or persistence of extramedullary disease after at least two cycles of chemotherapy. * First or subsequent relapse, including morphologic or MRD-detectable (≥1x10-4 ) bone marrow and/or extramedullary relapses after at least one standard frontline therapy. * Relapse after allogeneic haematopoietic stem cell transplantation (allo-HSCT). * Primary refractoriness, defined as either morphologic persistence or detectable MRD (≥1x10-4 ) after at least two cycles of chemotherapy, making the patient not candidate for allo-HSCT. 4. Patient without reproductive capacity or else, commitment to the use of a highly effective method of contraception during the study. Exclusion Criteria: 1. Limiting organ dysfunction, such as uncontrolled cardiac (e.g., depressed left ventricular ejection fraction (LVEF), \<45%), pulmonary, liver, renal or CNS dysfunction. 2. Allo-HSCT within a time frame \<3 months, or requiring continued immunosuppressive treatment for graft versus host disease (GvHD). 3. Uncontrolled epilepsy or underlying central nervous system (CNS) severe disease. 4. Active bacterial, fungal or viral infection not controlled by adequate treatment. 5. Known HIV, active hepatitis B (HBV), or hepatitis C virus (HCV) infection. 6. Women who are pregnant (urine/blood pregnancy test positive) or lactating. 7. Severe illness or medical condition, which would not permit the patient to be managed according to the protocol. 8. Suffering from a serious autoimmune disease or immunodeficiency disease. 9. The patient participated in other experimental drug clinical trial within 6 weeks prior to OC-1 infusion. 10. Other non-controlled concomitant neoplasms.
References
Publications (0)
Data not yet available
No reference posted for this study.