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OncoMatch/Clinical Trials/NCT07021677

Use of a New Medicine "Daratumumab" to Treat Left-over Cancer in a Blood Cancer Called "T Acute Lymphoblastic Leukemia"

Is NCT07021677 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies Daratumumab for t acute lymphoblastic leukemia.

Phase 2RecruitingTata Memorial CentreNCT07021677Data as of May 2026

Treatment: DaratumumabT-ALL (T-acute lymphoblastic leukemia) is an aggressive blood cancer, wherein patients who are MRD positive after two courses of induction chemotherapy have poor outcomes. This goal of this study is to determine if Daratumumab can make such T-ALL patients MRD negative. The main questions this study aims to answer are - 1. Whether MRD Positive T-ALL patients can become MRD negative after two doses of daratumumab? 2. Whether MRD Positive T-ALL patients can become MRD negative after four doses of daratumumab? 3. Whether addition of daratumumab can affect the risk of progression or death at 1-year? 4. Whether daratumumab is safe to use? Newly diagnosed patients of T-ALL who are MRD positive after two courses of induction chemotherapy will be eligible to receive daratumumab. These patients will receive two doses of weekly intravenous daratumumab at standard dose (16mg/kg), and will undergo repeat evaluation of MRD from bone marrow one week after the second dose of daratumumab. Patients who become MRD negative will continue chemotherapy as per institutional policy. Those who remain MRD positive will be eligible to receive two additional doses, and will undergo another bone marrow MRD testing one week after the fourth dose. Irrespective of the results after the fourth dose, patients will be continued on chemotherapy as per institutional policy.

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Extracted eligibility criteria

Cancer type

Acute Lymphoblastic Leukemia

Biomarker criteria

Required: CD38 positive (positive)

Performance status

ECOG 0–2(Ambulatory, capable of self-care)

Prior therapy

Must have received: induction chemotherapy — CR-1

assessed on BM after two phases of induction chemotherapy in CR-1

Lab requirements

Liver function

Total bilirubin <2x ULN; AST/ALT <3x ULN

Cardiac function

NYHA Class III or IV cardiac disease, or LVEF <40% [excluded]

Total bilirubin <2 times upper limit of normal (ULN); AST/ALT <3 ULN; NYHA Class III or IV cardiac disease, or left ventricular ejection fraction <40%

Structured fields extracted by AI. May contain errors — verify against the official protocol.

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