TABLE 2.
Major drugs in clinical development for treatment of COVID‐19
| Drug | Mechanism | Dosage and mode of administration | Side effects | Clinical trial |
|---|---|---|---|---|
|
Lopinavir/ritonavir
|
Protease inhibitors, that work together to block the viral replication | 400 mg/100 mg, 2 times/d (Oral) |
|
11 trials (for instance NCT04307693, 3/13/20) |
|
Remdesivir
|
Gets incorporated into viral RNA leading to RNA termination trouble and inhibition of viral replication. | 200 mg once for first day, followed by 100 mg/d (Intravenous) |
|
6 trials (eg, NCT04292899, 3/19/20) |
|
Favipiravir
|
RNA polymerase inhibitor | 1600 mg twice for 1 day followed by 600 mg 2 times/d (Oral) |
|
Atleast three trials (eg, NCT04303299 3/12/2020) |
|
Chloroquine
|
Interferes with the cellular receptor ACE2 and also impairs the acidification of endosomes, thereby impeding the virus trafficking inside the cells |
500 mg (300 mg for chloroquine) for 2 times/d (Oral) |
|
At least ten trials (eg, NCT04303507, 3/11/20; NCT04261517, 2/14/20) |
|
Ribavirin
|
Nucleoside analog of ribofuranose that inhibits viral RNA synthesis | 500 mg for 2‐3 times/d in combination with lopinavir/ritonavir or IFN‐α (Intravenous) |
|
At least 5 trials (NCT04254874, 2/5/20; ChiCTR2000029308, 1/23/20) |
|
Oseltamavir
|
Neuraminidase inhibitor | 12.5 mL of oral suspension or 75 mg capsule 2 times/d (Oral) |
|
One trial (NCT04261270, 2/7/20) |
|
Arbidol
|
Blocks viral fusion | 200 mg for 3 times/d (Oral) |
|
Two trials (NCT04260594,2/7/20; NCT04286503, 2/27/20) |