OncoMatch

OncoMatch/Clinical Trials/NCT06541444

Safety and Efficacy of NK520 to Treat Relapsed/Refractory Acute Myeloid Leukemia

Is NCT06541444 recruiting? Yes, currently enrolling (Jun 2026). This Early Phase 1 trial studies NK520 for relapsed/refractory acute myeloid leukemia.

Early Phase 1RecruitingBase Therapeutics (Shanghai) Co., Ltd.NCT06541444Data as of Jun 2026Location: China

Treatment: NK520This study will evaluate the safety and efficacy of NK520 in the treatment of relapsed/refractory acute myeloid leukemia. NK520 will be administered by intravenous injection. The safety and efficacy of this treatment will be evaluated.

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Extracted eligibility criteria

Treatments studied

Other

NK520

Cancer type

Acute Myeloid Leukemia

Performance status

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

Demographics

Ages ≤ 75

Prior therapy

Min 2 prior lines

Lab requirements

Blood counts

Normal Organ Function

Kidney function

Normal Organ Function

Liver function

Normal Organ Function

Normal Organ Function

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

Frequently asked questions

Is NCT06541444 currently recruiting?

Yes, this trial is currently recruiting patients.

Is there an age limit?

Yes. Patients must be 75 years or younger.

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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