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Movfor
- Ενεργό Συστατικό:
- Σε Απόθεμα: Μόνος 10 πακέτα αριστερά
- Ασθένεια:
- Movfor άλλα ονόματα:
Molnupiravir, μια από του στόματος αντιιική θεραπεία για τον COVID-19
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Movfor 200mg
Πακέτο Ανά χάπι Ειδική τιμή 200 καψάκια Δωρεάν Ταχεία Παράδοση $5.49 $1466 -26% Μόνο $1097 160 καψάκια Δωρεάν Ταχεία Παράδοση $5.60 $1173 -24% Μόνο $896 120 καψάκια Δωρεάν Ταχεία Παράδοση $5.79 $880 -21% Μόνο $695 80 καψάκια Δωρεάν Ταχεία Παράδοση $6.18 $587 -16% Μόνο $494 40 καψάκια Δωρεάν Κανονική Παράδοση $7.33 Μόνο $293
Product Description
Common use
Easily distributed oral antivirals are urgently needed to treat coronavirus disease-2019 (COVID-19), prevent progression to severe illness, and block transmission of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). We report the results of a Phase 2a trial evaluating the safety, tolerability, and antiviral efficacy of molnupiravir in the treatment of COVID-19.
Dosage and direction
Eligible participants included outpatients with confirmed SARS-CoV-2 infection and symptom onset within 7 days. Participants were randomized 1:1 to 200 mg molnupiravir or placebo, or 3:1 to molnupiravir (400 or 800 mg) or placebo, twice-daily for 5 days.
Antiviral activity was assessed as time to undetectable levels of viral RNA by reverse transcriptase polymerase chain reaction and time to elimination of infectious virus isolation from nasopharyngeal swabs.
Results
Among 202 treated participants, virus isolation was significantly lower in participants receiving 800 mg molnupiravir (1.9%) versus placebo (16.7%) at Day 3 (p = 0.02). At Day 5, virus was not isolated from any participants receiving 400 or 800 mg molnupiravir, versus 11.1% of those receiving placebo (p = 0.03). Time to viral RNA clearance was decreased and a greater proportion overall achieved clearance in participants administered 800 mg molnupiravir versus placebo (p = 0.01). Molnupiravir was generally well tolerated, with similar numbers of adverse events across all groups.
Conclusions
Molnupiravir is the first oral, direct-acting antiviral shown to be highly effective at reducing nasopharyngeal SARS-CoV-2 infectious virus and viral RNA and has a favorable safety and tolerability profile.
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