NATDAC (daclatasvir) / NATCO, Hetero 
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  • ||||||||||  NATDAC (daclatasvir) / NATCO, Hetero
    Journal:  Impact of oral antiviral therapy against HCV on gut microbiota. A prospective study. (Pubmed Central) -  Jun 2, 2023   
    All were treated with DAAs for 12 weeks (5 with Paritaprevir-Ombitasvir-Ritonavir-Dasabuvir, 3 with Sofosbuvir-Ledipasvir, 1 with Sofosbuvir-Ribavirin, 1 with Sofosbuvir-Daclatasvir, 1 with Sofosbuvir-Velpatasvir) and 100% achieved SVR12...Our study shows that viral eradication obtained with DAA is associated with a trend in restoring the heterogeneity of ?-diversity and in reducing the percentage of potentially pathogenic microbial species, although this benefit is less evident in patients with cirrhosis. Further studies with larger sample size are needed to confirm these data.
  • ||||||||||  Daklinza (daclatasvir) / BMS, NATDAC (daclatasvir) / NATCO, Hetero
    Retrospective data, Review, Journal:  Efficacy and Safety of Sofosbuvir-based Regimens in Hepatitis C Patients With Decompensated Cirrhosis: A Systematic Review and Meta-analysis. (Pubmed Central) -  Nov 22, 2022   
    Patients on SOF/velpatasvir±ribavirin achieved a significantly higher SVR (91.0%, 95% CI: 87.7-93.9) than that of SOF/ledipasvir±ribavirin [(86.3%, 95% CI: 84.6-87.8); p=0.004)], or on SOF/daclatasvir±ribavirin (82.4%, 95% CI: 78.2-86.2%; p<0.001)...There was no publication bias. The analysis found that 12 weeks of SOF/velpatasvir without ribavirin is the preferred therapy, with a significantly higher SVR compared with other SOF-based regimens in decompensated HCV patients.
  • ||||||||||  Actemra IV (tocilizumab) / Roche, JW Pharma
    Retrospective data, Review, Journal:  Comparative efficacy and safety of pharmacological interventions for the treatment of COVID-19: A systematic review and network meta-analysis. (Pubmed Central) -  Jan 16, 2021   
    Hydroxychloroquine did not provide clinical benefits while posing cardiac safety risks when combined with azithromycin, especially in the vulnerable population. Only 29% of current evidence on pharmacological management of COVID-19 is supported by moderate or high certainty and can be translated to practice and policy; the remaining 71% are of low or very low certainty and warrant further studies to establish firm conclusions.
  • ||||||||||  paritaprevir/ritonavir (ABT-450/r) / AbbVie, Daklinza (daclatasvir) / BMS
    Clinical, Journal, Real-World Evidence:  Direct antiviral therapy for treatment of hepatitis C: A real-world study from Brazil. (Pubmed Central) -  Sep 30, 2020   
    Policies should encourage treatment for all Chronic HCV infected patients with sofosbuvir based regimens in Asia and Africa. SOF-based DAA regimens are effective and safe in the heterogeneous highly admixed Brazilian population and could remain an option for HCV treatment at least in low-income countries.
  • ||||||||||  velpatasvir (GS-5816) / Gilead, Daklinza (daclatasvir) / BMS
    Clinical, Journal:  Frequent antiviral treatment failures in patients infected with hepatitis C virus genotype 4, subtype 4r. (Pubmed Central) -  May 23, 2020   
    The lower rates of SVR in patients infected with subtype 4r are related to the frequent preexistence at treatment baseline and subsequent selection by DAA treatment of both NS5A and NS5B S282 RASs. Our study suggests that these patients should be identified and receive a triple DAA combination regimen as first-line treatment.