1. Patients aged above 18 years either gender with positive RT-PCR for novel Corona Virus causing Covid-19 pandemic. <br/ >2.Only patients categorized as suffering from uncomplicated illness (category 1), mild pneumonia (category 2) and severe pneumonia (category 3) as defined by ICMR dt. 31-03-2020, will be selected to participate in the study. <br/ >3.Women of childbearing potential must agree to use contraception for the duration of the study. <br/ >4.Patients or their legally acceptable representative willing to sign the informed Consent form.

1. Patients aged above 18 years either gender with positive RT-PCR for novel Corona Virus causing Covid-19 pandemic. <br/ >2.Only patients categorized as suffering from uncomplicated illness (category 1), mild pneumonia (category 2) and severe pneumonia (category 3) as defined by ICMR dt. 31-03-2020, will be selected to participate in the study. <br/ >3.Women of childbearing potential must agree to use contraception for the duration of the study. <br/ >4.Patients or their legally acceptable representative willing to sign the informed Consent form.

1. Patients aged above 18 years either gender with positive RT-PCR for novel Corona Virus causing Covid-19 pandemic. <br/ >2.Only patients categorized as suffering from uncomplicated illness (category 1), mild pneumonia (category 2) and severe pneumonia (category 3) as defined by ICMR dt. 31-03-2020, will be selected to participate in the study. <br/ >3.Women of childbearing potential must agree to use contraception for the duration of the study. <br/ >4.Patients or their legally acceptable representative willing to sign the informed Consent form.

1. Patients aged above 18 years either gender with positive RT-PCR for novel Corona Virus causing Covid-19 pandemic. <br/ >2.Only patients categorized as suffering from uncomplicated illness (category 1), mild pneumonia (category 2) and severe pneumonia (category 3) as defined by ICMR dt. 31-03-2020, will be selected to participate in the study. <br/ >3.Women of childbearing potential must agree to use contraception for the duration of the study. <br/ >4.Patients or their legally acceptable representative willing to sign the informed Consent form.