Table 4.
Ongoing clinical trials of therapeutic drugs for SARS-CoV-2
Drugs | Role | References |
---|---|---|
Antiviral Medications (Blockage of the virus entry) | ||
Chloroquine & Hydroxychloroquine |
Block virus infection by increasing endosomal pH Reduce the viral copy number of SARS-CoV-2 Combination of hydroxychloroquine and azithromycin demonstrated positive effect |
[144] [132] |
Viral RNA synthesis inhibitors | ||
Remdesivir |
Antiviral activities against the single stranded RNA viruses Inhibit the infection and pathology of MERS-CoV and SARS-CoV-II |
[145] [146] |
Favipiravir | Functions as an inhibitor of the RNA-dependent RNA polymerase by structurally resembling the endogenous guanine | [147] |
Lopinavir—ritonavir combination | Inhibiting HIV-1 protease for protein cleavage, resulting in non-infectious, immature viral particles |
[148] [149] [150] |
Ivermectin |
Anti-parasitic agent Reduce viral RNA up to 5000-fold after 48 h of infection with SARS-CoV-2 |
[151] [152] [153] |
Darunavir | Anti-retroviral protease inhibitor uses in combination drugs such as ritonavir or cobicistat |
[154] [155] |
Blocking Virus–Cell Membrane Fusion | ||
Recombinant Human Angiotensin-converting Enzyme 2 (rhACE2) |
Blocking the S protein of SARS-CoV2 from interacting with the cellular ACE2 rhACE2 could inhibit SARS-CoV-2 replication in cellular and embryonic stem decreased serum level of angiotensin II |
[156] |
Arbidol Hydrochloride (Umifenovir) | Entry inhibitor against influenza viruses and arboviruses |
[157] [158] |