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OncoMatch/Clinical Trials/NCT06584006

Thymalfasin and Recombinant Human IL-2 Injections in Treating Lymphocytopenia for Patients With Malignant Hematological Tumors

Is NCT06584006 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies multiple treatments including Thymalfasin for and Recombinant Human Interleukin-2 Injections for hematological malignancy.

Phase 2RecruitingThe First Affiliated Hospital of Xiamen UniversityNCT06584006Data as of Jun 2026Location: China

Treatment: Thymalfasin for · Recombinant Human Interleukin-2 InjectionsTo evaluate the efficacy and safety of Thymalfasin for injection in combination with Recombinant Human Interleukin-2 Injections in the treatment of lymphocytopenia in patients with malignant hematological tumors

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Extracted eligibility criteria

Treatments studied

Other

Thymalfasin forRecombinant Human Interleukin-2 Injections

Cancer type

Acute Myeloid Leukemia

Acute Lymphoblastic Leukemia

Non-Hodgkin Lymphoma

Multiple Myeloma

Myelodysplastic Syndrome

Chronic Lymphocytic Leukemia

Performance status

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

Prior therapy

Cannot have received: chemotherapy

Within 8 days after chemotherapy for lymphoma and within 14 days after chemotherapy for AML

Cannot have received: immunosuppressive treatment (cyclosporine, corticosteroids, ruxolitinib, JAK1/2 inhibitors)

Immunosuppressive treatment (such as cyclosporine, corticosteroids, ruxolitinib, JAK1/2 inhibitors, etc.) within the past 5 days

Cannot have received: allogeneic hematopoietic stem cell transplantation

Patients who have undergone allogeneic hematopoietic stem cell transplantation

Lab requirements

Blood counts

Tumor involvement in the bone marrow leading to hematopoietic suppression (neutrophils <1.0×10^9/L, HB<70g/L, PLT<50×10^9/L) [excluded]

Kidney function

Estimated creatinine clearance rate ≥ 30 mL/min.

Liver function

AST and ALT ≤ 3.0 x ULN. Bilirubin ≤ 1.5 x ULN.

Estimated creatinine clearance rate ≥ 30 mL/min. AST and ALT ≤ 3.0 x ULN. Bilirubin ≤ 1.5 x ULN. Tumor involvement in the bone marrow leading to hematopoietic suppression (neutrophils <1.0×10^9/L, HB<70g/L, PLT<50×10^9/L) [excluded]

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

Frequently asked questions

Is NCT06584006 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior chemotherapy, immunosuppressive treatment, allogeneic hematopoietic stem cell transplantation disqualifies patients from enrollment.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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