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Clinical Trial NCT07485504 for Relapsed or Refractory Hematologic Malignancies is not yet recruiting. See the Trial Radar Card View and AI discovery tools for all the details. Or ask anything here. | ||
Safety and Efficacy of DIT101 in Relapsed or Refractory Hematologic Malignancies Phase 1 15 Cell Therapy Open-Label Long-Term Follow-up
DIT101 is an investigational in vivo CAR-T cell therapy administered by intravenous infusion. After administration, it is intended to generate CAR-T cells within the patient's body that can reco...
Show MoreA Prospective, Single-Arm Study Evaluating the Safety and Efficacy of DIT101 in Subjects With Relapsed or Refractory Hematologic Malignancies
- DIT101-IBL001
| Participant Group/Arm | Intervention/Treatment |
|---|---|
ExperimentalIn Vivo CAR-T Therapy for Relapsed or Refractory Hematologic Malignancies Participants with relapsed or refractory hematologic malignancies will receive 1-2 intraveneous administrations of in Vivo CAR-T (DIT101). | In Vivo CAR-T Therapy Participants will receive 1 intravenous administration of DIT101, according to the study dosing regimen. A second dose at the same dose may be administered to eligible participants who show no response after initial treatment, upon sponsor approval. |
| Outcome Measure | Measure Description | Time Frame |
|---|---|---|
Safety#Incidence and severity of adverse events (AEs) | To evaluate the possible adverse events after DIT101 infusion, including the incidence, and severity of AEs | 2 years after completion of the DIT101 infusion or until death, whichever occurs first. |
Safety#Incidence of Dose Limiting Toxicity (DLT) | Incidence of dose limiting toxicities (DLTs) within 28 days after the first DIT101 infusion. | 28 days after the first DIT101 infusion. |
| Outcome Measure | Measure Description | Time Frame |
|---|---|---|
Duration of Remission (DOR) | Time from first achievement of Complete Response(CR), Complete Response with incomplete hematologic recovery(CRi) or Partial Response(PR) to disease relapse or death due to leukemia. | 2 years after completion of the DIT101 infusion or until death, whichever occurs first. |
Event-Free Survival (EFS) | Time from DIT101 infusion to earliest occurrence of any event: death after response, relapse, non-response, or treatment discontinuation due to leukemia- or treatment-related death, adverse events, or new anti-cancer therapy (excluding bridging hematopoietic stem cell transplantation (HSCT). | 2 years after completion of the DIT101 infusion or until death, whichever occurs first. |
Leukemia-Free Survival (LFS) | Time from first achievement of CR/CRi to disease relapse or death. | 2 years after completion of the DIT101 infusion or until death, whichever occurs first. |
Proportion of Responding Subjects Receiving HSCT | Percentage of subjects who achieve remission after DIT101 infusion and subsequently undergo hematopoietic stem cell transplantation. | Up to 2 years following the completion of DIT101 infusion. |
Overall Survival (OS) | Time from first DIT101 infusion to death from any cause. | Up to 2 years after DIT101 infusion or until death, whichever occurs first. |
Maximum Concentration (Cmax) of CAR-T Cells in Peripheral Blood | To evaluate the peak expansion level of CAR-T cells in peripheral blood following DIT101 infusion. | up to 2 years after completion of the DIT101 infusion or until death, whichever occurs first. |
Adults aged 18 to <70 years, any gender.
Voluntarily provide written informed consent and willing to comply with all study procedures.
Diagnosed with relapsed or refractory B-cell acute lymphoblastic leukemia/lymphoma (B-ALL/LBL), or other relapsed/refractory hematologic malignancies as judged by the investigator and confirmed by the collaborating institution.
Tumor cells confirmed positive for the target antigen by immunophenotyping.
Bone marrow blast ≥5% at screening and/or presence of extramedullary disease.
For B-ALL/LBL patients, meets criteria for relapsed/refractory disease, including:
- Primary refractory after ≥2 cycles of standard chemotherapy or not achieving CR after multiple salvage regimens;
- Relapse within 12 months after CR or ≥12 months relapse after CR not achieving CR after subsequent standard therapy;
- Relapse after hematopoietic stem cell transplantation;
- Relapse after prior CAR-T therapy targeting the same antigen.
ECOG performance status 0-2.
Expected survival >3 months.
Adequate organ function, including:
- Renal: creatinine clearance >45 mL/min;
- Hepatic: total bilirubin ≤3×ULN, ALT/AST ≤5×ULN;
- Coagulation: PT, APTT, or INR ≤1.5×ULN;
- Cardiac: LVEF ≥50% within 1 month;
- Pulmonary: SpO₂ ≥92% at rest on room air;
- Hematologic and immune function considered sufficient to tolerate study treatment.
Women of childbearing potential must have a negative pregnancy test; women considered not of childbearing potential include those who are postmenopausal for ≥12 months or have undergone surgical sterilization (hysterectomy or bilateral oophorectomy).
Pregnant or breastfeeding women.
Known hereditary bone marrow failure syndromes (e.g., Fanconi anemia, Kostmann syndrome, Shwachman syndrome, or other known marrow failure syndromes).
Uncontrolled active central nervous system leukemia (CNSL; CNS2 or CNS3).
Prior anti-cancer therapy before screening, including:
- Systemic chemotherapy within 1 week;
- Systemic immunotherapy/targeted therapy (monoclonal antibodies, bispecific antibodies, ADCs, etc.) with last dose <5 half-lives or <4 weeks (whichever is shorter);
- Donor lymphocyte infusion within 6 weeks;
- CAR-T therapy or hematopoietic stem cell transplantation within 3 months;
- Radiotherapy within 4 weeks (unless bone marrow reserve >5% and investigator judges it does not affect eligibility);
- Persistent clinically significant toxicity from prior therapy not recovered to ≤CTCAE Grade 1 (except alopecia).
Uncontrolled severe active infection.
History of significant cardiac disease, including: severe heart failure (NYHA class III-IV), myocardial infarction or PCI/stent within 12 months, unstable angina, QTc >480 ms, or other clinically significant arrhythmia per investigator judgment.
History of CNS injury, seizure, stroke, or brain hemorrhage requiring treatment within 6 months.
Active viral infections:
- HIV antibody positive, syphilis serology positive;
- HBsAg >10⁶ IU/mL;
- HCV antibody positive;
- EBV positive (EBER or copy number above normal).
Need for long-term systemic corticosteroid therapy during DIT-101 infusion (local or inhaled steroids allowed).
Active autoimmune disease requiring treatment, immunodeficiency, or use of immunosuppressive therapy.
Acute or moderate-to-severe chronic graft-versus-host disease (GvHD) within 4 weeks prior to screening.
Known severe allergy to any component of DIT-101.
Women of childbearing potential or men unable to use effective contraception during DIT-101 infusion and for 1 year post-infusion; plans for pregnancy within 1 year post-infusion in male or female subjects or their partners.
Any condition that, in the investigator's opinion, may increase risk or interfere with study outcomes.
Prior malignancy other than hematologic malignancy, except:
- Malignancy treated with curative intent and disease-free ≥2 years;
- Non-melanoma skin cancer adequately treated with no current evidence of disease.
Tcelltech Inc.