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Principal Investigator


National Taiwan University Hospital (在職)

Division of Dermatology

Division of Hematology & Oncology

Division of Obstetrics & Gynecology

更新時間：2025-12-17

廖怡華LIAO, YI-HUA
  • Principal Investigator
  • Clinical Trial Experience (year) 8 years

Recruiting Trial

12Cases

篩選

Developmental Phase

  • Phase I

  • Phase I/II

  • Phase II

  • Phase II/III

  • Phase III

  • Phase IV

  • Others

Trial Status

  • Not yet recruiting

  • Active

  • Completed

Recruitment Status

  • Not yet recruiting

  • Recruiting

  • Completed

  • Terminated

  • Stop recruiting

  • Suspended

  • Study ended

Trial scale

  • Multi-Regional Multi-Center

  • Taiwan Multiple Center

  • Taiwan Single Center

The expected start time interval of the test

-

Trial Applicant

  • Hospital/Foundation

  • Pharmaceutical/Biopharmaceutical company

  • Contract Research Organization

Important Roles

  • Asia Regional PI

  • Taiwan National PI

  • Chairman/Global PI

  • Steering Committee

  • Advisory board

  • None

Audit by Sponsors/CRO

  • Sponsors

  • CRO

  • None

Investigator-initiated trial(IIT)

  • Yes

Filters

廖怡華

List

21Cases

2021-06-25 - 2024-01-04

Phase III

Completed

  • Condition/Disease

  • Test Drug

Participate Sites
3Sites

Recruiting3Sites

2025-03-01 - 2028-09-01

Phase III

Not yet recruiting

  • Condition/Disease

  • Test Drug

Participate Sites
3Sites

Recruiting3Sites

2019-04-26 - 2023-04-23

Phase III

Completed
A Randomized, Double-blind, Multi-center Study Assessing Short (16 Weeks) and Long-term Efficacy (up to 1 Year), Safety, and Tolerability of 2 Subcutaneous Secukinumab Dose Regimens in Adult Patients With Moderate to Severe Hidradenitis Suppurativa (SUNSHINE).

  • Condition/Disease

    Moderate to Severe Hidradenitis Suppurativa

  • Test Drug

    Cosentyx

Participate Sites
2Sites

Recruiting2Sites

2026-06-01 - 2028-12-31

Phase III

Not yet recruiting

  • Condition/Disease

  • Test Drug

Participate Sites
4Sites

Not yet recruiting4Sites

2020-08-01 - 2025-12-04

Phase III

Active

  • Condition/Disease

  • Test Drug

Participate Sites
2Sites

Recruiting2Sites

2014-01-01 - 2017-12-31

Phase II

  • Condition/Disease

  • Test Drug

Participate Sites
1Sites

Terminated1Sites

2021-04-01 - 2022-07-31

Phase II/III

A Phase 2/3, multi-center, double-blind, placebo-controlled, randomized, parallel-group, dose-response comparison of the efficacy and safety of a topical rapamycin cream for the treatment of facial angiofibromas (FA) associated with Tuberous Sclerosis Complex (TSC) in patients 6 years of age and over.

  • Condition/Disease

    facial angiofibromas (FA) associated with Tuberous Sclerosis Complex (TSC)

  • Test Drug

    Rapamycin

Participate Sites
1Sites

Recruiting1Sites

2019-04-01 - 2020-01-02

Others

A Phase Ib, Open Label, Multicenter Study of the Safety and Efficacy of MIW815 (ADU-S100) Administered by Intratumoral Injection With PDR001 to Patients With Advanced/Metastatic Solid Tumors or Lymphomas

  • Condition/Disease

    Advanced/Metastatic Solid Tumors or Lymphomas

  • Test Drug

    MIW815 (ADU-S100) , PRD001

Participate Sites
1Sites

Terminated1Sites

2019-08-01 - 2021-12-31

Phase III

BOTOX® (onabotulinumtoxinA) Treatment of Masseter Muscle Prominence: A Phase 3, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study

  • Condition/Disease

    Masseter Muscle Prominence

  • Test Drug

    BOTOX®

Participate Sites
4Sites

Terminated4Sites

2017-09-21 - 2021-10-14

Phase III

A Randomized, Parallel-group, Multicenter Study to Assess the Efficacy and Safety of Vilaprisan in Subjects With Uterine Fibroids

  • Condition/Disease

    Uterine Fibroids

  • Test Drug

    Vilaprisan (BAY 1002670)

Participate Sites
8Sites

Terminated8Sites

1 2 3
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