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Principal Investigator


Taipei Veterans General Hospital (在職)

Division of Cardiovascular Diseases

Division of Urology

Division of Hematology & Oncology

Taipei WanFang Hospital (Managed by Taipei Medical Univeristy) (在職)

Division of Thoracic Medicine

Division of Hematology & Oncology

Division of Thoracic Medicine

Division of Hematology & Oncology

更新時間:2023-09-19

邱宗傑Chiou, Tzeon-jye
  • Principal Investigator
  • Clinical Trial Experience (year) 22 years 9 個月

篩選

List

93Cases

2012-11-01 - 2017-03-31

Phase III

  • Condition/Disease

  • Test Drug

Participate Sites
5Sites

Terminated5Sites

2006-10-01 - 2010-06-30

Phase III

  • Condition/Disease

  • Test Drug

Participate Sites
3Sites

Terminated3Sites

2023-09-01 - 2023-12-31

Phase I/II

A Phase 1/2 Open Label, Multicenter, Dose Escalation and Expansion Study of the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of HM43239 in Patients With Relapsed or Refractory Acute Myeloid Leukemia (AML)
  • Condition/Disease

    Relapsed or Refractory Acute Myeloid Leukemia

  • Test Drug

    HM43239

Participate Sites
3Sites

Terminated3Sites

2010-09-15 - 2016-12-31

Phase III

  • Condition/Disease

  • Test Drug

Participate Sites
3Sites

Terminated3Sites

2013-04-16 - 2015-06-30

Phase III

A Phase III, randomised, observer-blind, placebocontrolled, multicentre study to assess the safety and immunogenicity of GSK Biologicals’ Herpes Zoster HZ/su candidate vaccine when administered intramuscularly on a two-dose schedule to adults aged 18 years and older with haematologic malignancies.
  • Condition/Disease

    Prevention of Herpes Zoster (HZ) and related complications in adults ≥50 years of age and immunocompromised adults ≥18 years of age. The current study will be performed in immunocompromised adults ≥18 years of age.

  • Test Drug

    gE/AS01B Vaccine

Participate Sites
4Sites

Terminated3Sites

Study ended1Sites

葉士芃
China Medical University Hospital

Division of Hematology & Oncology

2009-03-01 - 2010-12-31

Phase II

  • Condition/Disease

  • Test Drug

Participate Sites
3Sites

Terminated3Sites

2009-03-01 - 2010-12-31

Phase II

  • Condition/Disease

  • Test Drug

Participate Sites
3Sites

Terminated3Sites

2017-10-01 - 2025-01-31

Phase III

A Multicenter, Randomized, Double-blind, Placebo-controlled Phase 3 Study of the Bruton’s Tyrosine Kinase (BTK) Inhibitor, Ibrutinib, in Combination with Rituximab versus Placebo in Combination with Rituximab in Treatment Naïve Subjects with Follicular Lymphoma
  • Condition/Disease

    Follicular lymphoma tumors (grades 1-3A) that have never received treatment meet the Groupe d'Etude des Lymphomes Folliculaire (GELF) treatment standards: elderly people over 70 years old, or 60-69 years old with complications

  • Test Drug

    Ibrutinib (PCI-32765)

Participate Sites
6Sites

Recruiting6Sites

2016-05-01 - 2019-09-30

Phase I

A Phase 1/1b, Open-label Study of Pevonedistat (MLN4924, TAK-924) as Single Agent and in Combination with Azacitidine in Adult East Asian Patients with Acute Myeloid Leukemia (AML) or Myelodysplastic Syndromes (MDS)
  • Condition/Disease

    Acute Myeloid Leukemia (AML) or Myelodysplastic Syndromes (MDS)

  • Test Drug

    Pevonedistat (MLN4924, TAK-924)

Participate Sites
2Sites

Terminated2Sites