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Prediction based on a novel high-throughput precision medication detection technology system - Refractory Relapsed Acute Myeloid Leukemia Treatment Response Study

Prediction based on a novel high-throughput precision medication detection technology system - Refractory Relapsed Acute Myeloid Leukemia Treatment Response Study

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500099682
Enrollment
Unknown
Registered
2025-03-27
Start date
2025-04-01
Completion date
Unknown
Last updated
2025-03-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Myeloid Leukemia

Interventions

Treatment group for refractory/relapsed AML using novel HDS technology:Treatment guided by effective drug predictions based on the novel HDS detection technology system.
Treatment Based on Prior Medication and 2023 NCCN AML Guidelines:Treatment Based on Prior Medication and 2023 NCCN AML Guidelines

Sponsors

The Second Affiliated Hospital of Army Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1: Patients with refractory or relapsed AML 2: No gender restriction; age 18–70 years; Karnofsky Performance Status (KPS) score >60; estimated survival >3 months 3: No severe impairment of major organ functions: Creatinine 55% Hemoglobin >90 g/L, bilirubin <2.0 mg/dL 4: No uncontrolled severe infections or severe graft-versus-host disease (GVHD) 5: Voluntary participation with signed informed consent

Exclusion criteria

Exclusion criteria: 1: Severe cardiac, renal, or hepatic dysfunction. 2: Concurrent malignancy requiring treatment. 3: Clinical symptoms of brain dysfunction or severe psychiatric disorders preventing understanding or compliance with the study protocol. 4: Inability to adhere to follow-up schedules. 5: Inability to complete required treatment plans and follow-up observations. 6: History of severe acute allergic reactions. 7: Participation in other clinical trials. 8: Other conditions deemed unsuitable for clinical trials by investigators.

Design outcomes

Secondary

MeasureTime frame
effectivity;security;Overall Survival(OS);Leukemia-Free Survival(LFS);

Primary

MeasureTime frame
Objective Response Rate(ORR);

Countries

China

Contacts

Public ContactLei Gao

The Second Affiliated Hospital of Army Medical University

gaolei7765@163.com+86 132 2868 9635

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026