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Principal Investigator


Linkou Chang Gung Medical Foundation (在職)

Division of Dermatology

Division of Others-Immunodermatology, Adverse drug reactions, Drug hypersensitivity, Pharmacogenomics

Division of General Internal Medicine

Taipei Chang Gung Medical Foundation (在職)

Division of Dermatology

Division of Others-Immunodermatology, Adverse drug reactions, Drug hypersensitivity, Pharmacogenomicspsoriasis,

Chang Gung Medical Foundation Chang Gung Memorial Hospital, Keelung

Division of Dermatology

更新時間：2023-10-24

鐘文宏Chung, Wen-Hung
  • Principal Investigator
  • Clinical Trial Experience (year) 17 years 9 個月

  • chung1@cgmh.org.tw

Recruiting Trial

46Cases

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

鐘文宏

Taipei Chang Gung Medical Foundation

Division of Dermatology

List

2Cases

2019-06-01 - 2025-12-31

Phase III

Completed
A Multicenter, Randomized, Double-Blind, Placebo- Controlled, Phase 3 Study to Evaluate the Efficacy and Safety of Baricitinib in Adult Patients With Severe or Very Severe Alopecia Areata

  • Condition/Disease

    Alopecia Areata

  • Test Drug

    Baricitinib (LY3009104)Baricitinib (LY3009104)Baricitinib (LY3009104)

Participate Sites
4Sites

Terminated4Sites

2020-05-01 - 2023-05-01

Phase II

Effisayil™ 2: Multi-center, Randomized, Parallel Group, Double Blind, Placebo Controlled, Phase IIb Dose-finding Study to Evaluate Efficacy and Safety of BI 655130 (Spesolimab) Compared to Placebo in Preventing Generalized Pustular Psoriasis (GPP) Flares in Patients With History of GPP

  • Condition/Disease

    Generalized Pustular Psoriasis

  • Test Drug

    BI 655130 (Spesolimab)

Participate Sites
3Sites

Not yet recruiting1Sites

Recruiting1Sites

Terminated1Sites

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