RecruitingEarly Phase 1NCT06541444
Safety and Efficacy of NK520 to Treat Relapsed/Refractory Acute Myeloid Leukemia
Studying Megakaryoblastic acute myeloid leukemia with t(1;22)(p13;q13)
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Base Therapeutics (Shanghai) Co., Ltd.
- Principal Investigator
- zhiguo LongShanghai Pudong Hospital
- Intervention
- NK520(drug)
- Enrollment
- 9 target
- Eligibility
- 18-75 years · All sexes
- Timeline
- 2024 – 2026
Study locations (1)
- Shanghai Pudong Hospital, Shanghai, Shanghai Municipality, China
Collaborators
Shanghai Pudong Hospital
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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