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#nirmatrelvir — Public Fediverse posts

Live and recent posts from across the Fediverse tagged #nirmatrelvir, aggregated by home.social.

  1. Extended #nirmatrelvir–ritonavir #treatment durations for immunocompromised #patients with #COVID19 (EPIC-IC): a placebo-controlled, randomised, double-blind, phase 2 trial, etidiohnew.blogspot.com/2025/0

  2. Well… #Dinner last night. Neither of us ate.

    I woke not long ago with a stomach ache though. A good burp seems to have fixed that.

    The last of my #Paxlovid #nirmatrelvir #ritonavir has been taken.

    My Dr is now on holiday, so I guess I just wait & see what happens with my #Covid.

    Still have a few days of #BellsPalsy meds left. My lips have been very active the last few days, doing their #MexicanWave at random times.

    More rain inbound. I’ll feed the #alpacas & #sheep before it arrives.

  3. #Nirmatrelvir–ritonavir versus placebo–ritonavir in individuals with #longCOVID in the #USA (PAX LC): a double-blind, randomised, placebo-controlled, phase 2, decentralised trial, etidiohnew.blogspot.com/2025/0

  4. #Structural and #virologic #mechanism of the emergence of #resistance to #Mpro #inhibitors in #SARS-CoV-2, PNAS: pnas.org/doi/abs/10.1073/pnas.

    We generated SARS-CoV-2 variants resistant to three SARS-CoV-2 main protease (Mpro) inhibitors (#nirmatrelvir, TKB245, and 5h), by propagating the ancestral SARS-CoV-2WK521WT in VeroE6TMPRSS2 cells with increasing concentrations of each inhibitor and examined their structural and virologic profiles.

  5. Oral #Nirmatrelvir–Ritonavir as #Postexposure #Prophylaxis for #Covid19, N Engl J Med.: nejm.org/doi/full/10.1056/NEJM

    In this placebo-controlled trial, postexposure prophylaxis with nirmatrelvir–ritonavir for 5 or 10 days did not significantly reduce the #risk of symptomatic #SARS-CoV-2 infection. (Funded by Pfizer; ClinicalTrials.gov number, NCT05047601.)

  6. Oral #Nirmatrelvir–Ritonavir as #Postexposure #Prophylaxis for #Covid19, N Engl J Med.: nejm.org/doi/full/10.1056/NEJM

    In this placebo-controlled trial, postexposure prophylaxis with nirmatrelvir–ritonavir for 5 or 10 days did not significantly reduce the #risk of symptomatic #SARS-CoV-2 infection. (Funded by Pfizer; ClinicalTrials.gov number, NCT05047601.)

  7. Oral #Nirmatrelvir–Ritonavir as #Postexposure #Prophylaxis for #Covid19, N Engl J Med.: nejm.org/doi/full/10.1056/NEJM

    In this placebo-controlled trial, postexposure prophylaxis with nirmatrelvir–ritonavir for 5 or 10 days did not significantly reduce the #risk of symptomatic #SARS-CoV-2 infection. (Funded by Pfizer; ClinicalTrials.gov number, NCT05047601.)

  8. Oral #Nirmatrelvir–Ritonavir as #Postexposure #Prophylaxis for #Covid19, N Engl J Med.: nejm.org/doi/full/10.1056/NEJM

    In this placebo-controlled trial, postexposure prophylaxis with nirmatrelvir–ritonavir for 5 or 10 days did not significantly reduce the #risk of symptomatic #SARS-CoV-2 infection. (Funded by Pfizer; ClinicalTrials.gov number, NCT05047601.)

  9. Oral #Nirmatrelvir–Ritonavir as #Postexposure #Prophylaxis for #Covid19, N Engl J Med.: nejm.org/doi/full/10.1056/NEJM

    In this placebo-controlled trial, postexposure prophylaxis with nirmatrelvir–ritonavir for 5 or 10 days did not significantly reduce the #risk of symptomatic #SARS-CoV-2 infection. (Funded by Pfizer; ClinicalTrials.gov number, NCT05047601.)

  10. Comparative #effectiveness of #combination #therapy with #nirmatrelvir–ritonavir & #remdesivir versus #monotherapy with remdesivir or nirmatrelvir–ritonavir in patients hospitalised with #COVID19: a target #trial emulation study thelancet.com/journals/laninf/

    Our study highlighted the potential for reduced #risk of #mortality, #ICU admission, or need for ventilatory support in patients hospitalised with COVID-19 treated with nirmatrelvir–ritonavir as a monotherapy ...

  11. Comparative #effectiveness of #combination #therapy with #nirmatrelvir–ritonavir & #remdesivir versus #monotherapy with remdesivir or nirmatrelvir–ritonavir in patients hospitalised with #COVID19: a target #trial emulation study thelancet.com/journals/laninf/

    Our study highlighted the potential for reduced #risk of #mortality, #ICU admission, or need for ventilatory support in patients hospitalised with COVID-19 treated with nirmatrelvir–ritonavir as a monotherapy ...

  12. Comparative #effectiveness of #combination #therapy with #nirmatrelvir–ritonavir & #remdesivir versus #monotherapy with remdesivir or nirmatrelvir–ritonavir in patients hospitalised with #COVID19: a target #trial emulation study thelancet.com/journals/laninf/

    Our study highlighted the potential for reduced #risk of #mortality, #ICU admission, or need for ventilatory support in patients hospitalised with COVID-19 treated with nirmatrelvir–ritonavir as a monotherapy ...

  13. Comparative #effectiveness of #combination #therapy with #nirmatrelvir–ritonavir & #remdesivir versus #monotherapy with remdesivir or nirmatrelvir–ritonavir in patients hospitalised with #COVID19: a target #trial emulation study thelancet.com/journals/laninf/

    Our study highlighted the potential for reduced #risk of #mortality, #ICU admission, or need for ventilatory support in patients hospitalised with COVID-19 treated with nirmatrelvir–ritonavir as a monotherapy ...

  14. Comparative #effectiveness of #combination #therapy with #nirmatrelvir–ritonavir & #remdesivir versus #monotherapy with remdesivir or nirmatrelvir–ritonavir in patients hospitalised with #COVID19: a target #trial emulation study thelancet.com/journals/laninf/

    Our study highlighted the potential for reduced #risk of #mortality, #ICU admission, or need for ventilatory support in patients hospitalised with COVID-19 treated with nirmatrelvir–ritonavir as a monotherapy ...

  15. A unifying #model to explain frequent #SARS-CoV-2 #rebound after #nirmatrelvir #treatment and limited prophylactic #efficacy nature.com/articles/s41467-024

    Here authors develop a mathematical model for viral-immune dynamics & nirmatrelvir #pharmacokinetics and suggest that early treatment preserves susceptible cells & blunts innate immune response without fully eliminating infection. They project that treatment extension for 10 days may overcome this effect.

  16. A unifying #model to explain frequent #SARS-CoV-2 #rebound after #nirmatrelvir #treatment and limited prophylactic #efficacy nature.com/articles/s41467-024

    Here authors develop a mathematical model for viral-immune dynamics & nirmatrelvir #pharmacokinetics and suggest that early treatment preserves susceptible cells & blunts innate immune response without fully eliminating infection. They project that treatment extension for 10 days may overcome this effect.

  17. A unifying #model to explain frequent #SARS-CoV-2 #rebound after #nirmatrelvir #treatment and limited prophylactic #efficacy nature.com/articles/s41467-024

    Here authors develop a mathematical model for viral-immune dynamics & nirmatrelvir #pharmacokinetics and suggest that early treatment preserves susceptible cells & blunts innate immune response without fully eliminating infection. They project that treatment extension for 10 days may overcome this effect.

  18. A unifying #model to explain frequent #SARS-CoV-2 #rebound after #nirmatrelvir #treatment and limited prophylactic #efficacy nature.com/articles/s41467-024

    Here authors develop a mathematical model for viral-immune dynamics & nirmatrelvir #pharmacokinetics and suggest that early treatment preserves susceptible cells & blunts innate immune response without fully eliminating infection. They project that treatment extension for 10 days may overcome this effect.

  19. A unifying #model to explain frequent #SARS-CoV-2 #rebound after #nirmatrelvir #treatment and limited prophylactic #efficacy nature.com/articles/s41467-024

    Here authors develop a mathematical model for viral-immune dynamics & nirmatrelvir #pharmacokinetics and suggest that early treatment preserves susceptible cells & blunts innate immune response without fully eliminating infection. They project that treatment extension for 10 days may overcome this effect.

  20. #Nirmatrelvir #Resistance in an Immunocompromised #Patient with Persistent #COVI19, Viruses: mdpi.com/1999-4915/16/5/718

    The impact of drug-resistant SARS-CoV-2 on the #clinical course, including its #severity, remains unknown. Our study is important for examining the clinical impact of nirmatrelvir resistance in COVID-19.

  21. "#Paxlovid ® ab sofort in der regulären Handelskette

    Bislang wurde die Versorgung mit der antiviralen Wirkstoffkombi #Nirmatrelvir/#Ritonavir aus Beständen bedient, die vom Bund beschafft wurden. Das ändert sich jetzt."

    #Corona #Coronavirus #COVID19 #LongCovid #PostCovid #MECFS #POTS

    aerztezeitung.de/Wirtschaft/Pa

  22. Harrington PR, Cong J, Troy SB, et al. #Evaluation of #SARS-CoV-2 #RNA #Rebound After #Nirmatrelvir/Ritonavir #Treatment in Randomized, Double-Blind, Placebo-Controlled Trials — #USA and International Sites, 2021–2022. MMWR Morb Mortal Wkly Rep 2023;72:1365–1370. DOI: dx.doi.org/10.15585/mmwr.mm725

  23. Effectiveness of #Nirmatrelvir#Ritonavir #Paxlovid Against the Development of #PostCOVID 19 Conditions Among U.S. Veterans

    t.ly/b1gfK

    “Out of 31 potential #PCCs, only combined thromboembolic events seemed to be reduced by nirmatrelvir–ritonavir”

    One of the authors does a 5-minute video at the link

    @longcovid
    #LongCovid #PwLC #PostCovidSyndrome #LC #PASC @covid19
    #COVIDー19 #COVID19 #COVID #COVID_19 #SARSCoV2 @novid #novid #CovidIsNotOver #CovidBrain

  24. ''WHO continues to strongly recommend #nirmatrelvir-ritonavir (also known by its brand name ‘#Paxlovid’) for people at high-risk and moderate #risk of hospitalization. The recommendations state that nirmatrelvir-ritonavir is considered the best choice for most eligible patients, given its therapeutic benefits, ease of administration and fewer concerns about potential harms. Nirmatrelvir-ritonavir was first recommended by WHO in April 2022''

  25. "I’m glad to see this paper - it’s a look from Pfizer about how they were able to scale up #nirmatrelvir (the antiviral component of the #Paxlovid combination) so quickly. The authors are surely correct when they say that this 17-month timeline is a record for the drug industry, and it’s very much worth seeing how this all happened."
    #Antiviral #drugdevelopment #covid19

    science.org/content/blog-post/

  26. 子陵在听歌
    2023-01-09 weibo.com/1251560221/MnseR2Rx3

    #新型冠状病毒 SARS-CoV-2是一个正链#RNA病毒,不是#逆转录病毒,它没有#逆转录酶#阿兹夫定 是一个活性不强的#HIV 逆转录酶#抑制剂,对SARS-CoV-2没有#抗病毒活性。而#Paxlovid 中的有效成分#Nirmatrelvir 是用最先进的#药化设计 方法根据SARS-CoV-2蛋白酶Mpro(3CL)#构象结构 修饰出来的(weibo.com/1251560221/LbrLu7UAZ )。

    阿兹夫定没有任何发表在#同行审阅 杂志上的有效性#临床试验 结果(weibo.com/7597822550/Mn9EBCRlo )。Paxlovid的有效性#3期临床试验 结果发表在全世界最权威的医学杂志#NEJM 上,是目前唯一能降低SARS-CoV-2#病毒载量 的#小分子抗病毒药weibo.com/1251560221/M4Ut7y5TQ );在其上市后多个独立的第三方机构在权威#医学杂志 上发表了其真实世界有效性数据。

    其实每个国家都有相关政策保护自己的#民族工业,对我而言,这并不陌生。如果去翻我之前的微博,我在微博上追踪了#抗病毒药 十几年,见证了很多重磅抗病毒药在#CDE#医保局 来来回回洽谈多年,比如#DTG#必妥维。HIV药物可以用几年来谈,但是在#重大传染病 #公共卫生 危机中,还用惯性方法去处理危机,可见一些机构的优先级是什么。当然,没有医学#科学训练、也非#医药卫生行业 从业者的人可能为此叫好,但接受过相关训练的从业者则无话可说。

    ———— ⁂ ————

    分析#阿兹夫定#临床试验数据:一个打死不冤的伪#新冠特效药

    Y博的科普园 一个生物狗的科普小园 2023-01-07 mp.weixin.qq.com/s/IrIfACWflj6

    申明:仅代表个人观点,不代表任何组织与单位

    这几天有报道说阿兹夫定的#三期临床试验 公布,显著缩短核酸转阴时间。这个药之前写过很多,#有效性极为可疑,安全性上的#遗传#生殖毒性 问题更无法解决(详见二条)。
    但很多人还在问,所以就去看了所谓显示有效的#巴西 三期临床试验,其实根本谈不上显示有效性,部分内容也与之前相关药企IPO文件里提到的其它#临床试验 结果冲突。此药能上架就已荒唐,如果你有(不)幸拿到阿兹夫定,扔了算了。