Study aim: Evaluation of the time to clinical recovery in the case with Dinvl in moderate-intensity pneumonia caused by Corona 19 compared with the control group Design: Randomized single blind, phase 3 clinical trial on 60 patients, The random number table was used for randomization Settings and conduct: This study was performed in hospitals, Baqiat Allah, in Tehran, on patients with moderate-intensity pneumonia caused by covid 19. Participants/Inclusion and exclusion criteria: Inclusion criteria up18 year-olds with moderate-intensity pneumonia caused by Covid 19 whose disease has been proven on the basis of CT scan or PCR evidence and have signed a participation form. Exclusion criteria All people who are prohibited from taking Dinvl or similar compounds or who are likely to have severe side effects if taken Dinvl. Intervention groups: Patients with inclusion criteria in the intervention group, in addition to the usual treatment, are treated daily with dinvl for 7 consecutive days. In the control group, the usual treatment for covid 19 infection. Main outcome variables: Time to clinical recovery 14 days readmission Rate Time to intubation Intubation rate 28 days survival rate side effects caused by dinvl