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Study identifier: NCT06541444 Synced from ClinicalTrials.gov · August 06, 2026
● Study status: Recruiting

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

Condition: Relapsed/Refractory Acute Myeloid Leukemia  ·  Sponsor: Base Therapeutics (Shanghai) Co., Ltd.

PhaseEARLY_Phase 1
Planned participants9
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersNo

About this study

This 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.

This description comes directly from the study's public registry record.

Talk to the study team

Jun Yan  ·  13817651474  ·  yanjun@basetherapeutics.com

Always discuss trial participation with your own doctor first.

Locations (1)

Shanghai Pudong HospitalShanghai, Shanghai Municipality, ChinaRecruiting

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