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Genomic Sequencing Study for Acute Myeloid Leukemia

A Feasibility Study of Amoy Myeloid Panel (R) (a targeted genomic sequencing kit) in Optimizing Diagnosis of Acute Myeloid Leukemia: Hematologic Malignancies (HM)-SCREEN-Japan 02 - HM02

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000046371
Enrollment
200
Registered
2022-01-17
Start date
2022-01-17
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Acute myeloid leukemia

Interventions

None listed

Sponsors

National Cancer Center East Department of Hematology
Lead Sponsor
Amoy Diagnostics
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Histologically or cytologically diagnosed with AML 2. Adult patient who are able to give his/her consent.

Exclusion criteria

Exclusion criteria: 1. Clinically inappropriate to join this study. 2. Absent leukemic cells in both the bone marrow and the peripheral blood.

Design outcomes

Primary

MeasureTime frame
Concordance of the clinical diagnosis and the genomic information.

Secondary

MeasureTime frame
Frequency and distribution of genomic abnormalities. Overall survival

Countries

Japan

Contacts

Public ContactSungGi Chi

National Cancer Center East Department of Hematology

schi@east.ncc.go.jp04-7133-1111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026