Table 5.
Drug Name | Mechanism of Action | NCT Number | Title | Study Population | Targeted Enrollment | Study Design | Primary Outcome Measure |
---|---|---|---|---|---|---|---|
Lopinavir + ritonavir; ribavirin; IFN-β1b | Antiretroviral and immunomodulatory | NCT04276688 | Lopinavir/Ritonavir, Ribavirin and IFN-beta Combination for nCoV Treatment | Age ≥18 yrs hospitalized for virologically confirmed 2019-nCoV infection with NEWS ≥1 on recruitment; febrile with symptoms and duration of symptoms ≤10 days | 127 | Randomized, open-label (1:1:1) to lopinavir + ritonavir; or ribavirin; or IFN-β1b | Time to negative nasopharyngeal viral RT-PCR assessed up to 1 month |
Lopinavir + ritonavir; hydroxychloroquine | Antiretroviral and viral entry | NCT04307693 | Comparison of Lopinavir/Ritonavir or Hydroxychloroquine in Patients With Mild Coronavirus Disease (COVID-19) | Age 16–99 yrs with confirmed mild COVID-19 (NEWS 0–4) | 150 | Randomized, open-label (1:1:1) lopinavir + ritonavir; or hydroxychloroquine; or standard care | Viral load at hospital days 3, 5, 7, 10, 14, 18 |
Remdesivir + hydroxychloroquine; remdesivir; hydroxychloroquine | Antiretroviral and viral entry | NCT04321616 | Efficacy of Different Anti-viral Drugs in COVID-19 Infected Patients | Age ≥18 yrs with confirmed SARS-CoV-2 by RT-PCR, admitted to hospital or ICU | 700 | Randomized, Open-Label (1:1:1) remdesivir; or hydroxychloroquine; or remdesivir + hydroxychloroquine adaptive controlled design; comparison with standard of care | In-hospital mortality at 3 weeks |
Combinations of oseltamivir, chloroquine, darunavir, ritonavir, lopinavir, oseltamivir, favipiravir | Antiretroviral and viral entry | NCT04303299 | Various Combination of Protease Inhibitors, Oseltamivir, Favipiravir, and Hydroxychloroquine for Treatment of COVID19: A Randomized Control Trial (THDMS-COVID-19) | Age 16–100 yrs with COVID-19 diagnosis | 320 | Randomized, open-label, oseltamivir + chloroquine; or darunavir + ritonavir + oseltamivir; or lopinavir + ritonavir + oseltamivir; or favipiravir + lopinavir + ritonavir; or darunavir + ritonavir + oseltamivir + chloroquine; or darunavir + ritonavir + favipiravir + chloroquine | Time to negative detection of SARS-CoV-2 in nasopharyngeal swab at 24 weeks |
Favipiravir; chloroquine phosphate | Antiretroviral and viral entry | NCT04319900 | Clinical Trial of Favipiravir Tablets Combined With Chloroquine Phosphate in the Treatment of Novel Coronavirus Pneumonia | Age 18–75 yrs; diagnosed with nCoV pneumonia with a course of illness no more than 14 days; if the course is >14 days, no progression by chest radiograph within 7 days; respiratory symptoms; positive COVID-19 RT-PCR within 3 days | 150 | Randomized, double-blind 3-arm study of favipiravir + chloroquine; or favipiravir; or placebo | Time to improvement of respiratory symptoms Number of days of viral shedding Frequency of improvement of respiratory symptoms |
Remdesivir; lopinavir + ritonavir; IFN-β1a; hydroxychloroquine | Antiretroviral, viral entry, and immunomodulatory | NCT04315948 | Trial of Treatments for COVID-19 in Hospitalized Adults (DisCoVeRy) | Age ≥18 yrs, laboratory-confirmed SARS-CoV-2 infection as determined by RT-PCR or other assay <72 h prior to randomization, hospitalized patients with illness of any duration, and pulmonary exam abnormalities and pulse O2 ≤ 94%, requiring O2, or requiring mechanical ventilation, or acute respiratory failure requiring mechanical ventilation and/or supplemental O2 | 3,100 | Adaptive, randomized, open-label 1:1:1:1:1 to remdesivir; or lopinavir/ritonavir; or lopinavir/ritonavir + INF-β1α; or hydroxychloroquine; or standard of care | Percentage of subjects reporting disease severity on a 7-point ordinal clinical scale reflective of hospitalization and oxygenation status; or death at 15 days |
Favipiravir + tocilizumab | Antiretroviral and immunomodulatory | NCT04310228 | Favipiravir Combined With Tocilizumab in the Treatment of Corona Virus Disease 2019 | Age 18–65 yrs, COVID-19 diagnosis, increased IL-6 | 150 | Randomized, open-label (1:1:1) of favipiravir + tocilizumab; or favipiravir; or tocilizumab | Clinical cure rate at 3 months |