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TPIDB > Principal Investigator

Principal Investigator


Linkou Chang Gung Medical Foundation (在職)

Division of Family Medicine

Division of Endocrinology

Cathay General Hospital

Division of Family Medicine

更新時間:2023-09-19

莊海華Chuang, Hai-Hua
  • Principal Investigator
  • Clinical Trial Experience (year) -18 years -4 個月

篩選

List

7Cases

2026-01-01 - 2032-03-10

Phase III

Active
A Master Protocol for a Randomized, Controlled, Clinical Trial of Multiple Pharmacologic Agents in Adult Participants with Metabolic Dysfunction-Associated Steatotic Liver Disease who are at Increased Risk of Developing Major Adverse Liver Outcomes (SYNERGY-Outcomes)
  • Condition/Disease

    Metabolic Dysfunction-Associated Steatotic Liver Disease

  • Test Drug

    Retatrutide (LY3437943) Tirzepatide (LY3298176)

Participate Sites
15Sites

Not yet recruiting8Sites

Recruiting7Sites

2024-01-01 - 2026-12-31

Phase III

Active
-
  • Condition/Disease

    -

  • Test Drug

    -

Participate Sites
6Sites

Not yet recruiting5Sites

Recruiting1Sites

2024-01-01 - 2025-12-31

Phase IV

Completed
-
  • Condition/Disease

    -

  • Test Drug

    -

Participate Sites
11Sites

Terminated11Sites

2026-05-05 - 2029-01-08

Phase III

Active
Efficacy and safety of NNC0487-0111 s.c. once-weekly in participants with overweight or obesity, and obstructive sleep apnoea treated with positive airway pressure (AMAZE 4)
  • Condition/Disease

    Obesity, Obstructive Sleep Apnoea

  • Test Drug

    NNC0487-0111 B

Participate Sites
4Sites

Not yet recruiting4Sites

2026-05-05 - 2029-02-21

Phase III

Not yet recruiting
Efficacy and safety of NNC0487-0111 s.c. once-weekly in participants with overweight or obesity, and obstructive sleep apnoea not treated with positive airway pressure (AMAZE 3)
  • Condition/Disease

    Obesity, Obstructive Sleep Apnoea

  • Test Drug

    NNC0487-0111 B

Participate Sites
4Sites

Not yet recruiting4Sites

2018-10-15 - 2019-11-30

Phase III

A Phase III, Prospective, Randomized, Open-Labeled, Active-Controlled, Multi-Center Study to Evaluate the Safety and Immunogenicity of Quadrivalent Influenza Vaccine, GC FLU, in Adults Aged 20 to 50
  • Condition/Disease

    Influenza

  • Test Drug

    GCFLU Quadrivalent Pre-filled Syringe inj.

Participate Sites
4Sites

Terminated4Sites

2020-07-01 - 2024-01-03

Phase IV

  • Condition/Disease

  • Test Drug

Participate Sites
1Sites

Recruiting1Sites