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Developmental Phase

  • Phase I

  • Phase I/II

  • Phase II

  • Phase II/III

  • Phase III

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  • Not yet recruiting

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The expected start time interval of the test

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Trial Applicant

  • Hospital/Foundation

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Important Roles

  • Asia Regional PI

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Audit by Sponsors/CRO

  • Sponsors

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Investigator-initiated trial(IIT)

  • Yes

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Linkou Chang Gung Medical Foundation

List

2341Cases

2025-08-01 - 2028-12-31

Phase II

Active
A Phase 2a, Randomized, Double-blind, Placebo-controlled, Parallel-Group, Multicenter Study to Evaluate the Efficacy, Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Immunogenicity of ALXN1920 in Adult Participants with PMN (Primary Membranous Nephropathy) who are at a High Risk for Disease Progression

  • Condition/Disease

    Primary Membranous Nephropathy

  • Test Drug

    ALXN1920

Participate Sites
3Sites

Recruiting3Sites

2025-09-01 - 2028-09-30

Phase I

Active
AN OPEN-LABEL, MULTICENTER PHASE I STUDY TO EVALUATE THE SAFETY, TOLERABILITY, PHARMACOKINETICS, PHARMACODYNAMICS, AND PRELIMINARY ANTI-TUMOR ACTIVITY OF ALPS12 IN PATIENTS WITH EXTENSIVE STAGE SMALL CELL LUNG CANCER

  • Condition/Disease

    Extensive Stage Small Cell Lung Cancer

  • Test Drug

    ALPS12 Gazyva

Participate Sites
5Sites

Recruiting5Sites

2025-09-01 - 2028-09-01

Phase I/II

Completed
A Phase 1/2, First in Human Study of DCC 3116 as Monotherapy and in Combination with RAS/MAPK Pathway Inhibitors in Patients with Advanced or Metastatic Solid Tumors with RAS/MAPK Pathway Mutations

  • Condition/Disease

    Advanced or Metastatic Solid Tumors With RAS/MAPK Pathway Mutations

  • Test Drug

    DCC-3116

Participate Sites
4Sites

Recruiting4Sites

2018-06-01 - 2020-05-31

Phase I

Completed
A Phase 1A/1B, Open Label, Multiple Dose, Dose Escalation, and Expansion Study to Investigate the Safety, Pharmacokinetics, Food Effect, and Antitumor Activities of BGB-290 in Subjects with Advanced Solid Tumors

  • Condition/Disease

    For Participants With Advanced Solid Tumors Failed With Previous Lines of Treatment

  • Test Drug

    BGB-290

Participate Sites
5Sites

Terminated5Sites

2018-01-01 - 2030-12-31

Phase III

Active
A Multicenter, Randomized, Double-Blind, Placebo-Controlled 52-Week Maintenance and an Open-Label Extension Study of the Efficacy and Safety of Risankizumab in Subjects with Ulcerative Colitis

  • Condition/Disease

    Ulcerative Colitis (UC)

  • Test Drug

    risankizumab

Participate Sites
6Sites

Recruiting5Sites

Study ended1Sites

2018-01-15 - 2029-06-30

Phase III

Active
A Phase III, Randomized, Double-blind Trial of Platinum Doublet Chemotherapy +/- Pembrolizumab (MK-3475) as Neoadjuvant/Adjuvant Therapy for Participants with Resectable Stage II, IIIA, and Resectable IIIB(T3-4N2) Non-small Cell Lung Cancer (NSCLC) (KEYNOTE-671)

  • Condition/Disease

    Non-small Cell Lung Cancer

  • Test Drug

    KEYTRUDA

Participate Sites
7Sites

Not yet recruiting1Sites

Recruiting4Sites

2018-06-01 - 2027-06-30

Phase II/III

Active
A Phase 2/3, Randomized, Double-blind, Placebo- and Active-controlled, Parallel-group, Multicenter Protocol to Evaluate the Efficacy and Safety of Guselkumab in Participants with Moderately to Severely Active Crohn's Disease

  • Condition/Disease

    Moderately to Severely Active Crohn′s Disease

  • Test Drug

    guselkumab、ustekinumba

Participate Sites
4Sites

Recruiting4Sites

2017-05-01 - 2019-12-31

Phase III

Completed
A Long-Term, Open-Label Extension Study of the Safety and Tolerability of RVT-101 in Subjects with Alzheimer’s Disease

  • Condition/Disease

    Alzheimer’s Disease

  • Test Drug

    RVT-101

Participate Sites
2Sites

Terminated1Sites

Study ended1Sites

黃錦章
Linkou Chang Gung Medical Foundation

2026-03-15 - 2032-10-25

Phase III

Active
ROSETTA Lung-202: A randomized, double-blind, Phase 3 trial comparing pumitamig monotherapy with pembrolizumab as first-line treatment for participants with locally advanced or metastatic non-small cell lung cancer and PD-L1 expression ≥ 50%.

  • Condition/Disease

    Comparison of Pumitamig monotherapy versus Pembrolizumab as first-line treatment for participants with locally advanced or metastatic non-small cell lung cancer and PD-L1 expression ≥ 50%.

  • Test Drug

    BMS-986545

Participate Sites
5Sites

Recruiting5Sites

2026-03-16 - 2034-01-30

Phase III

Not yet recruiting
Efficacy, safety, and pharmacokinetics of once-weekly subcutaneous cagrilintide 2.4 mg as monotherapy and in combination with subcutaneous semaglutide 2.4 mg (CagriSema) for weight management in overweight or obese children and adolescents.

  • Condition/Disease

    Obesity

  • Test Drug

    Cagrilintide CagriSema Semaglutide

Participate Sites
4Sites

Recruiting4Sites

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