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Developmental Phase

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  • Not yet recruiting

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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

  • Pharmaceutical/Biopharmaceutical company

  • Contract Research Organization

Important Roles

  • Asia Regional PI

  • Taiwan National PI

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Audit by Sponsors/CRO

  • Sponsors

  • CRO

  • None

Investigator-initiated trial(IIT)

  • Yes

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5307Cases

2016-09-01 - 2021-12-31

Phase II

  • Condition/Disease

  • Test Drug

Participate Sites
0Sites

2016-07-01 - 2019-01-09

Phase II

PHASE II STUDY OF COMBINED TEMOZOLOMIDE AND TARGETED P53 GENE THERAPY (SGT-53) FOR TREATMENT OF PATIENTS WITH RECURRENT GLIOBLASTOMA

  • Condition/Disease

    GLIOBLASTOMA

  • Test Drug

    SGT-53

Participate Sites
1Sites

Study ended1Sites

周德陽
China Medical University Hospital

Division of Orthopedics

2018-04-13 - 2022-04-13

Phase II

A Randomized, Open-Label Study of Combinations of Standard and High Dose REGN2810 (Cemiplimab; Anti-PD-1 Antibody) and Ipilimumab (Anti-CTLA-4 Antibody) in the Second-Line Treatment of Patients With Advanced Non-Small Cell Lung Cancer

  • Condition/Disease

    Advanced Non-Small Cell Lung Carcinoma

  • Test Drug

    REGN2810

Participate Sites
5Sites

Terminated5Sites

邱昭華
Taipei Veterans General Hospital

Division of Hematology & Oncology

2017-12-01 - 2019-03-31

Phase II

A Phase 2, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Antiviral Activity, Clinical Outcomes, Safety, Tolerability, and Pharmacokinetics of Orally Administered Lumicitabine (JNJ-64041575) Regimens in Hospitalized Infants and Children Aged 28 Days to 36 Months Infected With Respiratory Syncytial Virus

  • Condition/Disease

    Respiratory Syncytial Viruses

  • Test Drug

    Lumicitabine (JNJ-64041575)

Participate Sites
3Sites

Terminated3Sites

2017-12-15 - 2021-08-25

Phase II

A Long-term Follow-up of Study 64041575RSV2004 to Evaluate the Impact of Lumicitabine (JNJ-64041575) on the Incidence of Asthma and/or Wheezing in Infants and Children With a History of Respiratory Syncytial Virus Infection

  • Condition/Disease

    Respiratory Syncytial Virus Infections

  • Test Drug

    Lumicitabine (JNJ-64041575)

Participate Sites
3Sites

Terminated3Sites

2018-01-31 - 2026-02-08

Phase III

A RANDOMIZED (1:1), DOUBLE-BLIND, MULTI-CENTER, PLACEBO CONTROLLED STUDY EVALUATING INTENSIVE CHEMOTHERAPY WITH OR WITHOUT GLASDEGIB (PF-04449913) OR AZACITIDINE (AZA) WITH OR WITHOUT GLASDEGIB IN PATIENTS WITH PREVIOUSLY UNTREATED ACUTE MYELOID LEUKEMIA

  • Condition/Disease

    Acute Myeloid Leukemia, AML

  • Test Drug

    Glasdegib (PF-04449913)

Participate Sites
5Sites

Recruiting5Sites

高志平
Taipei Veterans General Hospital

Division of Hematology & Oncology

2015-02-01 - 2016-12-31

Phase III

A Randomized, Double-Blind, Chronic Dosing (24 Weeks), Placebo-Controlled, Parallel Group, Multi-Center Study to Assess the Efficacy and Safety of PT003, PT005, and PT001 in Subjects with Moderate to Very Severe COPD, Compared with Placeb

  • Condition/Disease

    COPD

  • Test Drug

    Glycopyrronium and Fomoterol Fumarate Inhalation Aerosol

Participate Sites
6Sites

Terminated5Sites

杭良文
China Medical University Hospital-Taipei

未分科

2014-10-01 - 2018-12-31

Phase II

A Phase 2, Multi-Center, Randomised, Double-Blind, Ascending-Dose, Placebo-Controlled Clinical Study to Assess the Safety and Efficacy of Fostamatinib in the Treatment of IgA Nephropathy

  • Condition/Disease

    IgA Nephropathy

  • Test Drug

    Fostamatinib (R788)

Participate Sites
3Sites

Terminated3Sites

2017-05-01 - 2025-12-31

Others

AURORA: A Phase 3 Study to Evaluate the Efficacy and Safety of Cenicriviroc for the Treatment of Liver Fibrosis in Adult Subjects With Nonalcoholic Steatohepatitis

  • Condition/Disease

    Nonalcoholic Steatohepatitis

  • Test Drug

    CVC /150mg tablet

Participate Sites
13Sites

Not yet recruiting9Sites

Recruiting1Sites

Terminated1Sites

彭成元
China Medical University Hospital-Taipei

未分科

2017-09-04 - 2020-01-31

Phase I/II

A Phase 1b/2, Multi-Center, Double-Blind (Principal Investigators and Study Subjects Blinded, Sponsor Unblinded), Placebo-Controlled, Randomized, Single-Ascending Dose Study to Assess the Safety, Pharmacokinetics, and Pharmacodynamics of DS-1040b in Subjects With Acute Ischemic Stroke

  • Condition/Disease

    Acute Ischemic Stroke

  • Test Drug

    DS-1040b

Participate Sites
4Sites

Terminated4Sites

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