UnknownPhase 1NCT05641259
A Study to Assess Safety and Preliminary Efficacy of LP-108 Combined With Azacitidine In Subjects With AML, MDS, CMML
Studying Acute myelomonocytic leukemia
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
- Guangzhou Lupeng Pharmaceutical Company LTD.
- Principal Investigator
- Depei Wu, PhDFirst Affiliated Hospital of Soochow University
- Intervention
- LP-108(drug)
- Enrollment
- 198 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2023 – 2025
Study locations (3)
- The First Affiliated Hospital of Nanchang University, Nanchang, China
- First Affiliated Hospital of Soochow University, Suzhou, China
- Affiliated Tumor Hospital of Zhengzhou University, Henan Cancer Hospital, Zhengzhou, China
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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