lopinavir/ritonavir / Generic mfg. 
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 77 Diseases   69 Trials   69 Trials   4434 News 


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  • ||||||||||  lopinavir/ritonavir / Generic mfg.
    Lopinavir/Ritonavir post-exposure prophylaxis did not protect against Covid-19 () -  May 12, 2022 - Abstract #AIDS2022AIDS_1343;    
    We observed no signal that LPV/r has efficacy as SARS-CoV-2 PEP in this prematurely terminated trial. Possible reasons for the unexpected direction of the final results include small sample size and changes in behaviour in this unblinded trial.
  • ||||||||||  Isentress (raltegravir) / Merck (MSD)
    Uptake of raltegravir granules in newborns diagnosed with HIV in Zimbabwe during the COVID-19 pandemic () -  May 12, 2022 - Abstract #AIDS2022AIDS_805;    
    Lower than expected birth testing uptake and RAL usage were observed, in large part due to inconsistent supply chain and trained human resources shortages during COVID-19. Addressing health systems gaps for supply chain, staffing (training, retention, mentorship, and supervision), and ability to track HIV-positive newborns is needed to improve birth testing services and outcomes for HIV-exposed infants, timely ART initiation, and follow-up on optimized regimens.
  • ||||||||||  sulphadiazine / Generic mfg., pyrimethamine / Generic mfg., lopinavir/ritonavir / Generic mfg.
    Journal:  Effect of HIV aspartyl protease inhibitors on experimental infection with a cystogenic Me49 strain of Toxoplasma gondii. (Pubmed Central) -  May 6, 2022   
    We investigated the potential activity of L/R against experimental T. gondii infection with a cystogenic Me49 strain in mice, considering the role of IFN-γ and IL-10 in the neuropathology versus pyrimethamine-sulfadiazine combination therapy...Cerebral hypercellularity, perivascular inflammatory response, lymphoplasmacytic infiltrates and glial cellular reaction were ameliorated by L/R treatment. Herein, L/R was proved to possess promising preventive and therapeutic perspectives in chronic cerebral toxoplasmosis.
  • ||||||||||  lopinavir/ritonavir / Generic mfg.
    Trial primary completion date:  TREATNOW: Trial of Early Therapies During Non-hospitalized Outpatient Window for COVID-19 (clinicaltrials.gov) -  Apr 28, 2022   
    P2,  N=600, Active, not recruiting, 
    Based on our study results, HCQ shows no apparent advantage compared to LPV/r for preventing progression to severe disease in patients with COVID-19. Trial primary completion date: Apr 2022 --> Dec 2021
  • ||||||||||  ritonavir / Generic mfg., lopinavir/ritonavir / Generic mfg.
    Review, Journal, Adverse events:  Identification of Drug Interaction Adverse Events in Patients With COVID-19: A Systematic Review. (Pubmed Central) -  Apr 26, 2022   
    The main finding of this systematic review is that the use of drug interaction checkers could have identified several DDI-associated adverse drug reactions, including severe and life-threatening events. Both the interactions between the drugs used to treat COVID-19 and between the COVID-19 drugs and those already used by the patients should be evaluated.
  • ||||||||||  Retrospective data, Journal:  Antiviral Used among Non-Severe COVID-19 Cases in Relation to Time till Viral Clearance: A Retrospective Cohort Study. (Pubmed Central) -  Apr 24, 2022   
    The age and gender of patients did not significantly affect the rate of viral clearance regardless of the antiviral therapy administered, even when compared to patients who received symptomatic treatment only, with the exception of hydroxychloroquine (HCQ), azithromycin, and favipiravir, which increased the odds of a faster rate of viral clearance by 46% after adjustments. (4) No significant differences were observed regarding the time until viral clearance among non-severe COVID-19 patients following the prescription of different antiviral drugs.
  • ||||||||||  lopinavir/ritonavir / Generic mfg.
    Journal:  Development of Advanced 3D-Printed Solid Dosage Pediatric Formulations for HIV Treatment. (Pubmed Central) -  Apr 24, 2022   
    This work has demonstrated, for the first time, the feasibility of using direct powder extrusion 3D printing to manufacture personalized pediatric HIV dosage forms based on 6 mm spherical tablets. H-bonding between drugs and excipients (hydroxypropyl methylcellulose and polyethylene glycol) resulted in the formation of amorphous solid dispersions with a zero-order sustained release profile, opposite to the commercially available formulation Kaletra, which exhibited marked drug precipitation at the intestinal pH.
  • ||||||||||  Journal:  QTc interval prolongation in patients infected with SARS-CoV-2 and treated with antiviral drugs. (Pubmed Central) -  Apr 20, 2022   
    The use of antivirals caused an increase on the QTc interval after 72 h of treatment, being the QTc long in 36.3% of the patients, although no arrhythmic events were observed. The use of hydroxychloroquine and antivirals requires active QTc monitoring and it is recommended to discontinue treatment if QTc > 500 ms.
  • ||||||||||  lopinavir/ritonavir / Generic mfg.
    New P1 trial:  Lopinavir/Ritonavir in PLWH With High-Grade AIN (clinicaltrials.gov) -  Apr 19, 2022   
    P1,  N=30, Not yet recruiting, 
  • ||||||||||  ivermectin oral / Generic mfg.
    Clinical, Review, Journal:  Safety profile of COVID-19 drugs in a real clinical setting. (Pubmed Central) -  Apr 15, 2022   
    In contrast, ample well-conducted studies have approved the use of remdesivir, tocilizumab, and dexamethasone under certain conditions in COVID-19 patients. Consequently, it is significant to establish a strong surveillance system in order to monitor the proper safety and toxicity profile of the potential anti-COVID-19 drugs with good clinical outcomes.
  • ||||||||||  hydroxychloroquine / Generic mfg.
    Retrospective data, Review, Journal:  Repurposing of drugs for Covid-19: a systematic review and meta-analysis. (Pubmed Central) -  Apr 1, 2022   
    Further large clinical trials are required to achieve more reliable findings. A risk-benefit analysis is required on an individual basis to weigh out the potential improvement in clinical outcome and viral load reduction compared to the risks of the adverse events.
  • ||||||||||  Actemra IV (tocilizumab) / Roche, JW Pharma
    Trial completion date, Trial suspension:  ULTRA-COVID: Ultra Low Doses of Therapy With Radiation Applicated to COVID-19 (clinicaltrials.gov) -  Mar 29, 2022   
    P=N/A,  N=15, Suspended, 
    These patients should be carefully evaluated and followed up. Trial completion date: Apr 2021 --> Mar 2022 | Recruiting --> Suspended