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Clinical Trials List

Protocol NumberAS1411-C-203

2009-12-01 - 2011-12-31

Phase II

Terminated6

ICD-10C92.00

Acute myeloblastic leukemia, not having achieved remission

ICD-10C92.02

Acute myeloblastic leukemia, in relapse

ICD-10C92.40

Acute promyelocytic leukemia, not having achieved remission

ICD-10C92.42

Acute promyelocytic leukemia, in relapse

ICD-10C92.50

Acute myelomonocytic leukemia, not having achieved remission

ICD-10C92.52

Acute myelomonocytic leukemia, in relapse

ICD-10C92.60

Acute myeloid leukemia with 11q23-abnormality not having achieved remission

ICD-10C92.62

Acute myeloid leukemia with 11q23-abnormality in relapse

ICD-10C92.A0

Acute myeloid leukemia with multilineage dysplasia, not having achieved remission

ICD-10C92.A2

Acute myeloid leukemia with multilineage dysplasia, in relapse

ICD-10Z51.12

Encounter for antineoplastic immunotherapy

ICD-9205.00

Acute myeloid leukemia, without mention of remission

  • Trial Applicant

    QPS

  • Sponsor

  • Trial scale

    Multi-Regional Multi-Center

  • Update

    2025/08/20

Investigators and Locations

Principal Investigator Su-Peng Yeh Division of Hematology & Oncology

Co-Principal Investigator

The Actual Total Number of Participants Enrolled

0 Stop recruiting

Principal Investigator 曾成槐 Division of Hematology & Oncology

Co-Principal Investigator

The Actual Total Number of Participants Enrolled

0 Stop recruiting

Principal Investigator 張正雄 Division of Hematology & Oncology

Co-Principal Investigator

The Actual Total Number of Participants Enrolled

0 Stop recruiting

Principal Investigator

Co-Principal Investigator

The Actual Total Number of Participants Enrolled

0 Stop recruiting

Principal Investigator HSIN-AN HOU Division of Hematology & Oncology

Co-Principal Investigator

The Actual Total Number of Participants Enrolled

0 Stop recruiting

Principal Investigator

Co-Principal Investigator

The Actual Total Number of Participants Enrolled

0 Stop recruiting

Condition/Disease

Objectives

Test Drug

Active Ingredient

Dosage Form

Dosage

Endpoints

Inclution Criteria

The Estimated Number of Participants

  • Taiwan

    25 participants

  • Global

    90 participants