Table 1.
Included clinical trial studies and baseline characteristics among COVID-19 patients treated by IFN-β
| Author | Country | Mean age ± SD | Sex (male %) | Type of study | N of patients | Study groups | Treatment onset from symptom onset | Stage of disease | ICU admission | |
|---|---|---|---|---|---|---|---|---|---|---|
| Intervention | control | |||||||||
| Intervention/control | ||||||||||
| Rahmani et al. (2020) | Iran | 60 (47–73) | 59% | Open-label randomized clinical trial | 66 | IFN β-1b | Standard care (lopinavir/ritonavir or atazanavir/ritonavir plus hydroxychloroquine for 7–10 days) | Not reported | Severe | 42.42% vs. 66.66% |
| Dastan et al. (2020) | Iran | 58.55 ± 13.43 | 75% | Prospective non-controlled trial | 20 | IFN-β-1a + hydroxychloroquine (200 mg P.O. BID) and lopinavir/ritonavir (200/50 mg P.O.; two tablets QID) for 5 days | Non-controlled trial | 6.5 ± 2.8 days | Severe | Non-controlled |
| Monfared, et al. (2020) | Iran | IFN: 56.0 ± 16 Control: 59.5 ± 14 | 54.3% | Open-label randomized clinical trial | 81 (42 in the IFN and 39 in the control group) | IFN-β-1a + Hydroxychloroquine (400 mg BD in first day and then 200 mg BD) plus lopinavir/ritonavir 155(400 /100 mg BD) or atazanavir/ritonavir (300/100 mg daily) for 7-10 days+ 35.7% of patients received intravenous immunoglobulin (IVIG)+ 61.9% of patients received corticosteroids | Hydroxychloroquine (400 mg BD in first day and then 200 mg BD) plus lopinavir/ritonavir (400/100 mg BD) or atazanavir/ritonavir (300/100 mg daily) for 7–10 days. + 25.6% of patients received intravenous immunoglobulin(IVIG)+ 43.6% of patients received corticosteroids | 10 days | Severe | 45.23% vs 58.97% |
| Payandemehr, et al. (2020) | Iran | 55.5 | 60% | Investigator initiated, open-label, single-arm clinical trial | 20 | Not reported | hydroxychloroquine (200 mg twice daily), lopinavir/ritonavir (200/50mg four times daily), oseltamivir (75 mg, twice daily) and ribavirin (1200 mg twice daily) | <7 days | Moderate to severe symptoms | 10% |
| Fan-Ngai Hung et al. (2020) | Hong Kong | 52 | 54% | Multileft RCT | 127(2:1) | IFN-β-1b + lopinavir 400 mg and ritonavir 100 mg every 12 h, ribavirin 400 mg every 12 h | Lopinavir 400 mg and ritonavir 100 mg every 12 h | 5 days | Hospitalized (severe) | Time to early warning score of 0, days 4.0/8.0 (p=0.001) |