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TPIDB > Principal Investigator

Principal Investigator


National Taiwan University Hospital (在職)

Division of Infectious Disease

Division of General Internal Medicine

更新時間:2023-09-19

李南瑤Lee, Nan-Yao
  • Principal Investigator
  • Clinical Trial Experience (year) 17 years 9 個月
  • nanyao@mail.ncku.edu.tw

篩選

List

14Cases

2023-05-01 - 2024-04-29

Phase II

Completed
A Phase Ⅱ,Double-blind,Randomized,Controlled Study to Evaluate the Safety and Efficacy of Silmitasertib(CX-4945) in Hospitalized Adults with COVID-19
  • Condition/Disease

    Community-acquired Pneumonia 、SARS-CoV-2 -Associated Pneumonia 、Influenza With Pneumonia

  • Test Drug

    CX-4945

Participate Sites
1Sites

Recruiting1Sites

2008-01-01 - 2010-10-31

Others

Not yet recruiting
  • Condition/Disease

  • Test Drug

Participate Sites
10Sites

Terminated10Sites

2021-03-01 - 2028-03-31

Phase III

Completed
A Phase 3 Randomized, Active-Controlled, Double-Blind Clinical Study to Evaluate the Antiretroviral Activity, Safety, and Tolerability of Doravirine/Islatravir Once-Daily in HIV-1 Infected Treatment-Naïve Participants
  • Condition/Disease

    HIV-1 Infection

  • Test Drug

    MK-8591A [Doravirine (MK-1439) + Islatravir (MK-8591)]BiktarvyR

Participate Sites
3Sites

Not yet recruiting2Sites

Recruiting1Sites

2022-12-09 - 2029-06-30

Phase III

Active
Randomized, Double-blind, Placebo-controlled, Multicenter Phase 3 Study to Assess the Efficacy, Safety And Immunogenicity of Vaccination With ExPEC9V in the Prevention of Invasive Extraintestinal Pathogenic Escherichia Coli Disease in Adults Aged 60 Years And Older With a History of Urinary Tract Infection in the Past 2 Years
  • Condition/Disease

    Invasive Extraintestinal Pathogenic Escherichia Coli Disease (IED) Prevention

  • Test Drug

    ExPEC9V

Participate Sites
4Sites

Not yet recruiting3Sites

Recruiting1Sites

2019-01-01 - 2023-12-31

Phase III

A phase III, randomized, open-label, controlled trial to investigate the efficacy and safety of UB-421 monotherapy as substitution for stable antiretroviral therapy in HIV-1 infected adults
  • Condition/Disease

    HIV

  • Test Drug

    UB-421

Participate Sites
12Sites

Not yet recruiting10Sites

Recruiting1Sites

2016-09-01 - 2021-11-30

Phase III

A Phase III, randomised, double-blind, multicentre, parallel-group, non-inferiority study evaluating the efficacy, safety, and tolerability of dolutegravir plus lamivudine compared to dolutegravir plus tenofovir/emtricitabine in HIV-1-infected Treatment-naïve Adults adults
  • Condition/Disease

    Infection, Human Immunodeficiency Virus HIV Infections

  • Test Drug

    Dolutegravir(DTG),Lamivudine(3TC).Tenofovir(TDF )/emtricitabine(FTC)

Participate Sites
6Sites

Recruiting5Sites

Terminated1Sites

2012-02-01 - 2014-12-31

Phase III

  • Condition/Disease

  • Test Drug

Participate Sites
8Sites

Terminated8Sites

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