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OncoMatch/Clinical Trials/NCT07173595

A Phase I Study of QLS2309 Injection in Patients With CD70+ Relapsed/Refractory Hematologic Malignancies

Is NCT07173595 recruiting? Yes, currently enrolling (May 2026). This Phase 1 trial studies QLS2309 for relapsed or refractory hematologic malignancies.

Phase 1RecruitingQilu Pharmaceutical Co., Ltd.NCT07173595Data as of May 2026

Treatment: QLS2309This is a single-arm, open-label, multicenter, dose-escalation, dose-expansion and efficacy-expansion phase I clinical study to evaluate the tolerability, safety, pharmacokinetics and preliminary antitumor activity of QLS2309 injection in patients with CD70+ relapsed/refractory hematologic malignancies.

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Extracted eligibility criteria

Cancer type

Acute Myeloid Leukemia

Acute Lymphoblastic Leukemia

Non-Hodgkin Lymphoma

Multiple Myeloma

Myelodysplastic Syndrome

Chronic Lymphocytic Leukemia

Biomarker criteria

Required: CD70 overexpression (CD70+)

CD70+ relapsed/refractory hematologic malignancies

Performance status

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

Prior therapy

Cannot have received: CD70-related antibodies, antibody-conjugated drugs (ADCs) or cell therapy products

Prior treatment with CD70-related antibodies, antibody-conjugated drugs (ADCs) or cell therapy products

Cannot have received: chemotherapy, biological therapy, endocrine therapy, immunotherapy, monoclonal antibodies

Known history of chemotherapy, biological therapy, endocrine therapy, immunotherapy, monoclonal antibodies, etc. within 4 weeks

Lab requirements

Blood counts

Kidney function

Liver function

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

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