LIVIVO - The Search Portal for Life Sciences

zur deutschen Oberfläche wechseln
Advanced search

Search results

Result 1 - 7 of total 7

Search options

  1. Article ; Online: Pharmacokinetics of Favipiravir in Critically Ill Patients With COVID-19.

    Irie, Kei / Nakagawa, Atsushi / Fujita, Hirotoshi / Tamura, Ryo / Eto, Masaaki / Ikesue, Hiroaki / Muroi, Nobuyuki / Tomii, Keisuke / Hashida, Tohru

    Clinical and translational science

    2020  Volume 13, Issue 5, Page(s) 880–885

    Abstract: ... 19 treatment since March 2020 in Japan. However, the pharmacokinetics of FPV in critically ill ... in critically ill patients was much lower than that of healthy subjects in a previous clinical trial, which is ... liquid chromatography in patients with severe COVID-19 who were admitted to the intensive care unit and placed ...

    Abstract Since December 2019, a novel coronavirus (severe acute respiratory syndrome-coronavirus 2 (SARS-CoV-2)) infection has been rapidly spreading worldwide and causing the respiratory illness, coronavirus disease 2019 (COVID-19). The antiretroviral drug favipiravir (FPV) has been experimentally used for COVID-19 treatment since March 2020 in Japan. However, the pharmacokinetics of FPV in critically ill patients is unknown. We measured the serum concentration of FPV using high-performance liquid chromatography in patients with severe COVID-19 who were admitted to the intensive care unit and placed on mechanical ventilation. The patients were administered 1,600 mg of FPV twice daily on day 1, followed by 600 mg twice daily from day 2 to day 5 (or more if needed). Suspensions of FPV tablets were administered through a nasogastric tube. Seven patients were enrolled in this study. Forty-nine blood samples were obtained from the eligible patients to evaluate FPV concentration. The FPV trough (after 8-12 hours) concentrations of most samples were lower than the lower limit of quantification (1 µg/mL) and half-maximal effective concentration (9.7 µg/mL) against SARS-CoV-2 previously tested in vitro. FPV trough concentration in critically ill patients was much lower than that of healthy subjects in a previous clinical trial, which is a cause for great concern. Further study is required to determine the optimal strategy for treatment of patients with severe COVID-19.
    MeSH term(s) Adult ; Aged ; Amides/administration & dosage ; Amides/pharmacokinetics ; Betacoronavirus/isolation & purification ; COVID-19 ; Coronavirus Infections/blood ; Coronavirus Infections/diagnosis ; Coronavirus Infections/drug therapy ; Coronavirus Infections/virology ; Critical Illness/therapy ; Dose-Response Relationship, Drug ; Drug Administration Schedule ; Female ; Humans ; Intubation, Gastrointestinal ; Male ; Pandemics ; Pneumonia, Viral/blood ; Pneumonia, Viral/diagnosis ; Pneumonia, Viral/drug therapy ; Pneumonia, Viral/virology ; Pyrazines/administration & dosage ; Pyrazines/pharmacokinetics ; Respiration, Artificial ; SARS-CoV-2 ; Severity of Illness Index ; Suspensions ; Tablets ; Treatment Outcome
    Chemical Substances Amides ; Pyrazines ; Suspensions ; Tablets ; favipiravir (EW5GL2X7E0)
    Keywords covid19
    Language English
    Publishing date 2020-06-29
    Publishing country United States
    Document type Clinical Trial ; Journal Article
    ZDB-ID 2433157-0
    ISSN 1752-8062 ; 1752-8054
    ISSN (online) 1752-8062
    ISSN 1752-8054
    DOI 10.1111/cts.12827
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  2. Article ; Online: Pharmacokinetics of Favipiravir in Critically Ill Patients With COVID19

    Irie, Kei / Nakagawa, Atsushi / Fujita, Hirotoshi / Tamura, Ryo / Eto, Masaaki / Ikesue, Hiroaki / Muroi, Nobuyuki / Tomii, Keisuke / Hashida, Tohru

    Clinical and Translational Science ; ISSN 1752-8054 1752-8062

    2020  

    Keywords General Pharmacology, Toxicology and Pharmaceutics ; General Biochemistry, Genetics and Molecular Biology ; General Neuroscience ; General Medicine ; covid19
    Language English
    Publisher Wiley
    Publishing country us
    Document type Article ; Online
    DOI 10.1111/cts.12827
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

  3. Article: Pharmacokinetics of Favipiravir in Critically Ill Patients With COVID-19

    Irie, Kei / Nakagawa, Atsushi / Fujita, Hirotoshi / Tamura, Ryo / Eto, Masaaki / Ikesue, Hiroaki / Muroi, Nobuyuki / Tomii, Keisuke / Hashida, Tohru

    Clin Transl Sci

    Abstract: ... 19 treatment since March 2020 in Japan. However, the pharmacokinetics of FPV in critically ill ... in critically ill patients was much lower than that of healthy subjects in a previous clinical trial, which is ... liquid chromatography in patients with severe COVID-19 who were admitted to the intensive care unit and placed ...

    Abstract Since December 2019, a novel coronavirus (severe acute respiratory syndrome-coronavirus 2 (SARS-CoV-2)) infection has been rapidly spreading worldwide and causing the respiratory illness, coronavirus disease 2019 (COVID-19). The antiretroviral drug favipiravir (FPV) has been experimentally used for COVID-19 treatment since March 2020 in Japan. However, the pharmacokinetics of FPV in critically ill patients is unknown. We measured the serum concentration of FPV using high-performance liquid chromatography in patients with severe COVID-19 who were admitted to the intensive care unit and placed on mechanical ventilation. The patients were administered 1,600 mg of FPV twice daily on day 1, followed by 600 mg twice daily from day 2 to day 5 (or more if needed). Suspensions of FPV tablets were administered through a nasogastric tube. Seven patients were enrolled in this study. Forty-nine blood samples were obtained from the eligible patients to evaluate FPV concentration. The FPV trough (after 8-12 hours) concentrations of most samples were lower than the lower limit of quantification (1 µg/mL) and half-maximal effective concentration (9.7 µg/mL) against SARS-CoV-2 previously tested in vitro. FPV trough concentration in critically ill patients was much lower than that of healthy subjects in a previous clinical trial, which is a cause for great concern. Further study is required to determine the optimal strategy for treatment of patients with severe COVID-19.
    Keywords covid19
    Publisher WHO
    Document type Article
    Note WHO #Covidence: #436861
    Database COVID19

    Kategorien

  4. Article ; Online: Pharmacokinetics of Favipiravir in Critically Ill Patients With COVID19

    Kei Irie / Atsushi Nakagawa / Hirotoshi Fujita / Ryo Tamura / Masaaki Eto / Hiroaki Ikesue / Nobuyuki Muroi / Keisuke Tomii / Tohru Hashida

    Clinical and Translational Science, Vol 13, Iss 5, Pp 880-

    2020  Volume 885

    Abstract: ... 19 treatment since March 2020 in Japan. However, the pharmacokinetics of FPV in critically ill ... in critically ill patients was much lower than that of healthy subjects in a previous clinical trial, which is ... liquid chromatography in patients with severe COVID19 who were admitted to the intensive care unit and placed ...

    Abstract Since December 2019, a novel coronavirus (severe acute respiratory syndrome‐coronavirus 2 (SARS‐CoV‐2)) infection has been rapidly spreading worldwide and causing the respiratory illness, coronavirus disease 2019 (COVID19). The antiretroviral drug favipiravir (FPV) has been experimentally used for COVID19 treatment since March 2020 in Japan. However, the pharmacokinetics of FPV in critically ill patients is unknown. We measured the serum concentration of FPV using high‐performance liquid chromatography in patients with severe COVID19 who were admitted to the intensive care unit and placed on mechanical ventilation. The patients were administered 1,600 mg of FPV twice daily on day 1, followed by 600 mg twice daily from day 2 to day 5 (or more if needed). Suspensions of FPV tablets were administered through a nasogastric tube. Seven patients were enrolled in this study. Forty‐nine blood samples were obtained from the eligible patients to evaluate FPV concentration. The FPV trough (after 8–12 hours) concentrations of most samples were lower than the lower limit of quantification (1 µg/mL) and half‐maximal effective concentration (9.7 µg/mL) against SARS‐CoV‐2 previously tested in vitro. FPV trough concentration in critically ill patients was much lower than that of healthy subjects in a previous clinical trial, which is a cause for great concern. Further study is required to determine the optimal strategy for treatment of patients with severe COVID19.
    Keywords Therapeutics. Pharmacology ; RM1-950 ; Public aspects of medicine ; RA1-1270 ; covid19
    Subject code 610
    Language English
    Publishing date 2020-09-01T00:00:00Z
    Publisher Wiley
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

  5. Article ; Online: [Pharmacokinetic Study of Antiviral Drugs in Patients with COVID-19].

    Irie, Kei

    Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan

    2023  Volume 143, Issue 3, Page(s) 239–241

    Abstract: ... the pharmacokinetics of favipiravir in critically ill patients with COVID-19 was of concern, because critically ill ... a collaborative clinical study to evaluate the pharmacokinetics of favipiravir in patients with COVID-19 ... The blood concentration of favipiravir in patients with COVID-19 at Kobe City Medical Center ...

    Abstract The Faculty of Pharmaceutical Sciences, Kobe Gakuin University has collaborated in clinical research with Kobe City Medical Center General Hospital. In this university-medical institution collaboration, university faculty members discuss clinical problems with on-site pharmacists and doctors, and carry out clinical research to resolve these problems. During the coronavirus disease 2019 (COVID-19) pandemic, many patients with COVID-19 were treated at Kobe City Medical Center General Hospital. In February 2020, during the first increase in the number of patients with COVID-19 in Japan, treatment for COVID-19 was not established, and some existing anti-viral drugs, such as favipiravir, were experimentally used for COVID-19 treatment. However, since these drugs were not developed specifically for treating COVID-19, their pharmacokinetics have not been sufficiently studied. In particular, the pharmacokinetics of favipiravir in critically ill patients with COVID-19 was of concern, because critically ill patients have an urgent need for life-saving anti-viral drug treatment. Therefore, we conducted a collaborative clinical study to evaluate the pharmacokinetics of favipiravir in patients with COVID-19. The blood concentration of favipiravir in patients with COVID-19 at Kobe City Medical Center General Hospital was measured by lipid chromatography-tandem mass spectrometry at Kobe Gakuin University. Population pharmacokinetics analysis was then performed. In this symposium review, we introduce our pharmacokinetic study of antiviral drugs in patients with COVID-19, focusing on the university-medical institution collaboration. We believe collaborative clinical research will be useful for solving clinical issues and ensuring the effectiveness and safety of pharmacotherapies.
    MeSH term(s) Humans ; Antiviral Agents ; COVID-19 ; COVID-19 Drug Treatment ; Critical Illness
    Chemical Substances Antiviral Agents ; favipiravir (EW5GL2X7E0)
    Language Japanese
    Publishing date 2023-03-01
    Publishing country Japan
    Document type English Abstract ; Journal Article
    ZDB-ID 200514-1
    ISSN 1347-5231 ; 0031-6903 ; 0372-7750 ; 0919-2085 ; 0919-2131
    ISSN (online) 1347-5231
    ISSN 0031-6903 ; 0372-7750 ; 0919-2085 ; 0919-2131
    DOI 10.1248/yakushi.22-00169-1
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  6. Article ; Online: Phase 2a, open-label, dose-escalating, multi-center pharmacokinetic study of favipiravir (T-705) in combination with oseltamivir in patients with severe influenza.

    Wang, Yeming / Zhong, Wu / Salam, Alex / Tarning, Joel / Zhan, Qingyuan / Huang, Jian-An / Weng, Heng / Bai, Changqing / Ren, Yanhong / Yamada, Koichi / Wang, Dayan / Guo, Qiang / Fang, Qiongqiong / Tsutomu, Sakurai / Zou, Xiaohui / Li, Haibo / Gillesen, Annelies / Castle, Lyndsey / Chen, Cheng /
    Li, Hongyan / Zhen, Jing / Lu, Binghuai / Duan, Jun / Guo, Liping / Jiang, Jinfang / Cao, Ruiyuan / Fan, Guohui / Li, Jintong / Hayden, Frederick G / Wang, Chen / Horby, Peter / Cao, Bin

    EBioMedicine

    2020  Volume 62, Page(s) 103125

    Abstract: ... in COVID-19.: Methods: In this dose-escalating study, favipiravir pharmacokinetics and tolerability were ... assessed in critically ill influenza patients. Participants received one of two dosing regimens; Japan ... into the low dose group and 19 patients into the high dose group of the study. Favipiravir C: Conclusion ...

    Abstract Background: The pharmacokinetics and appropriate dose regimens of favipiravir are unknown in hospitalized influenza patients; such data are also needed to determine dosage selection for favipiravir trials in COVID-19.
    Methods: In this dose-escalating study, favipiravir pharmacokinetics and tolerability were assessed in critically ill influenza patients. Participants received one of two dosing regimens; Japan licensed dose (1600 mg BID on day 1 and 600 mg BID on the following days) and the higher dose (1800 mg/800 mg BID) trialed in uncomplicated influenza. The primary pharmacokinetic endpoint was the proportion of patients with a minimum observed plasma trough concentration (C
    Results: Sixteen patients were enrolled into the low dose group and 19 patients into the high dose group of the study. Favipiravir C
    Conclusion: The two dosing regimens proposed for uncomplicated influenza did not achieve our pre-defined treatment threshold.
    MeSH term(s) Aged ; Amides/administration & dosage ; Amides/pharmacokinetics ; Drug Therapy, Combination ; Female ; Humans ; Influenza, Human/blood ; Influenza, Human/drug therapy ; Male ; Middle Aged ; Oseltamivir/administration & dosage ; Oseltamivir/pharmacokinetics ; Pyrazines/administration & dosage ; Pyrazines/pharmacokinetics ; Severity of Illness Index
    Chemical Substances Amides ; Pyrazines ; Oseltamivir (20O93L6F9H) ; favipiravir (EW5GL2X7E0)
    Language English
    Publishing date 2020-11-22
    Publishing country Netherlands
    Document type Clinical Trial, Phase II ; Journal Article ; Multicenter Study
    ZDB-ID 2851331-9
    ISSN 2352-3964
    ISSN (online) 2352-3964
    DOI 10.1016/j.ebiom.2020.103125
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  7. Article ; Online: Phase 2a, open-label, dose-escalating, multi-center pharmacokinetic study of favipiravir (T-705) in combination with oseltamivir in patients with severe influenza

    Yeming Wang / Wu Zhong / Alex Salam / Joel Tarning / Qingyuan Zhan / Jian-an Huang / Heng Weng / Changqing Bai / Yanhong Ren / Koichi Yamada / Dayan Wang / Qiang Guo / Qiongqiong Fang / Sakurai Tsutomu / Xiaohui Zou / Haibo Li / Annelies Gillesen / Lyndsey Castle / Cheng Chen /
    Hongyan Li / Jing Zhen / Binghuai Lu / Jun Duan / Liping Guo / Jinfang Jiang / Ruiyuan Cao / Guohui Fan / Jintong Li / Frederick G. Hayden / Chen Wang / Peter Horby / Bin Cao

    EBioMedicine, Vol 62, Iss , Pp 103125- (2020)

    2020  

    Abstract: ... in COVID-19. Methods: In this dose-escalating study, favipiravir pharmacokinetics and tolerability were ... assessed in critically ill influenza patients. Participants received one of two dosing regimens; Japan ... concentrations. The two dosing regimens were well-tolerated in critical ill patients with influenza. Conclusion ...

    Abstract Background: The pharmacokinetics and appropriate dose regimens of favipiravir are unknown in hospitalized influenza patients; such data are also needed to determine dosage selection for favipiravir trials in COVID-19. Methods: In this dose-escalating study, favipiravir pharmacokinetics and tolerability were assessed in critically ill influenza patients. Participants received one of two dosing regimens; Japan licensed dose (1600 mg BID on day 1 and 600 mg BID on the following days) and the higher dose (1800 mg/800 mg BID) trialed in uncomplicated influenza. The primary pharmacokinetic endpoint was the proportion of patients with a minimum observed plasma trough concentration (Ctrough) ≥20 mg/L at all measured time points after the second dose. Results: Sixteen patients were enrolled into the low dose group and 19 patients into the high dose group of the study. Favipiravir Ctrough decreased significantly over time in both groups (p <0.01). Relative to day 2 (48 hrs), concentrations were 91.7% and 90.3% lower in the 1600/600 mg group and 79.3% and 89.5% lower in the 1800/800 mg group at day 7 and 10, respectively. In contrast, oseltamivir concentrations did not change significantly over time. A 2-compartment disposition model with first-order absorption and elimination described the observed favipiravir concentration-time data well. Modeling demonstrated that less than 50% of patients achieved Ctrough ≥20 mg/L for >80% of the duration of treatment of the two dose regimens evaluated (18.8% and 42.1% of patients for low and high dose regimen, respectively). Increasing the favipravir dosage predicted a higher proportion of patients reaching this threshold of 20 mg/L, suggesting that dosing regimens of ≥3600/2600 mg might be required for adequate concentrations. The two dosing regimens were well-tolerated in critical ill patients with influenza. Conclusion: The two dosing regimens proposed for uncomplicated influenza did not achieve our pre-defined treatment threshold.
    Keywords Favipiravir ; Pharmacokinetics ; Concentration ; Influenza ; COVID-19 ; Critical illness ; Medicine ; R ; Medicine (General) ; R5-920
    Subject code 610
    Language English
    Publishing date 2020-12-01T00:00:00Z
    Publisher Elsevier
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

To top