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TPIDB > Principal Investigator

Principal Investigator


National Taiwan University Hospital (在職)

Division of Pediatrics

Division of Others-Department of Laboratory Medicine

Division of General Internal Medicine

Division of Hematology & Oncology

更新時間:2023-09-19

楊永立YANG, YUNG-LI
  • Principal Investigator
  • Clinical Trial Experience (year) 17 years 9 個月

篩選

List

39Cases

2020-05-15 - 2023-02-09

Phase III

A Phase 3 Open-label, Multicenter Study of the Safety, Efficacy, and Pharmacokinetics of Intravenous Recombinant Coagulation Factor VIII Fc-von Willebrand Factor-XTEN Fusion Protein (rFVIIIFc-VWF-XTEN; BIVV001) in Previously Treated Pediatric Patients <12 Years of Age With Severe Hemophilia A
  • Condition/Disease

    Severe Hemophilia A

  • Test Drug

    BIVV001/250 IU BIVV001/500 IU BIVV001/1000 IU BIVV001/2000IU

Participate Sites
4Sites

Not yet recruiting3Sites

Recruiting1Sites

2017-01-20 - 2022-02-17

Phase III

A Randomized, Open-label, Safety and Efficacy Study of Ibrutinib in Pediatric and Young Adult Patients With Relapsed or Refractory Mature B-cell Non-Hodgkin Lymphoma
  • Condition/Disease

    Mature B-cell Non-Hodgkin Lymphoma

  • Test Drug

    Ibrutinib

Participate Sites
3Sites

Terminated3Sites

2015-05-01 - 2020-06-11

Phase II

ABT-414 alone or ABT-414 plus temozolomide versus lomustine or temozolomide for recurrent glioblastoma: a randomized phase II study of the EORTC Brain Tumor Group
  • Condition/Disease

    Glioblastoma Multiforme (GBM)

  • Test Drug

    ABT-414

Participate Sites
5Sites

Terminated5Sites

2021-11-01 - 2029-08-30

Phase III

  • Condition/Disease

  • Test Drug

Participate Sites
3Sites

Recruiting3Sites

2021-11-01 - 2029-03-30

Phase III

  • Condition/Disease

  • Test Drug

Participate Sites
2Sites

Recruiting2Sites

2018-03-18 - 2024-10-31

Others

  • Condition/Disease

  • Test Drug

Participate Sites
1Sites

Recruiting1Sites

2008-06-02 - 2009-12-31

Others

  • Condition/Disease

  • Test Drug

Participate Sites
1Sites

Terminated1Sites

2019-08-01 - 2027-08-31

Phase III

A PHASE 3B, OPEN-LABEL, SINGLE-ARM, ROLLOVER STUDY TO EVALUATE LONG-TERM SAFETY IN SUBJECTS WHO HAVE PARTICIPATED IN OTHER LUSPATERCEPT (ACE-536) CLINICAL TRIALS
  • Condition/Disease

    Thalassemia

  • Test Drug

    Luspatercept (ACE-536)

Participate Sites
3Sites

Recruiting2Sites

Terminated1Sites

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