Remdesivir |
Antiviral |
Remdesivir is a drug contact to combat the invasion of RNA polymerases |
Tests in clinical studies |
(M. F. Hossain et al. 2020a,b) |
Favipiravir |
Antiviral |
Favipiravir blocks viral polymerase RNA and thus stops viral replication |
Completed clinical studies proved efficacy |
(M. H. Rahman et al. 2020a,b) |
Convalescent plasma |
Antiviral |
Curated plasma contains defensive antibodies against SARS-CoV-2 |
Confirmed effectiveness |
(M. F. Hossain et al. 2020a,b; M. H. Rahman et al. 2020a,b) |
Lopinavir |
Antiviral |
HIV-approved protease inhibitors are lopinavir/ritonavir |
Inconsistency in clinical trial findings |
(Horby et al. 2020) |
EIDD-2801 |
Antiviral |
Drives mutagenesis and impedes viral replication integration throughout RNA synthesis EDI-2801 |
Clinical testing prepared |
(M. H. Rahman et al. 2020a,b) |
Ritonavir |
Antiviral |
Ritonavir is HIV-approved protease inhibitor |
Inconsistency in clinical trial findings |
(Owa et al. 2020) |
Ivermectin |
Antiviral |
To suppress the replication of the pseudorabies virus by inhibiting nuclear import of UL42 |
Confirmed effectiveness |
(Sharun, Dhama, et al. 2020)
|
Oseltamivir |
Antiviral |
Antiviral action is showed through selectively targeting conservative catalytic domain of RNA-dependent RNA polymerase (RdRp) |
Completed clinical studies proved efficacy |
(Rosa et al. 2020) |
Umifenovir |
Antiviral |
To block the virus-cell membrane fusion |
Completed clinical studies proved efficacy |
(Pécheur et al. 2016) |
Favipiravir |
Antiviral |
Antiviral action is showed through selectively targeting conservative catalytic domain of RdRp, interrupting nucleotide incorporation process amid viral RNA replication |
Confirmed effectiveness |
(Furuta et al. 2017) |
GC376 |
Protease inhibitor |
Blocks virus replication |
Confirmed effectiveness |
(Sharun et al. 2021) |
GC373 |
Protease inhibitor |
Blocks virus replication |
Confirmed effectiveness |
(Sharun et al. 2021) |