Created at Source Raw Value Validated value
Nov. 26, 2021, 10:30 p.m. oms

1. Pregnant or nursing female. <br/ >2. Patients with history of allergy, hypersensitivity, or any serious reaction to study medication <br/ >3. Patients with a concomitant medical condition, whose participation, in the opinion of the investigator, may create an unacceptable additional risk. <br/ >4. Patient previously enrolled into this study. <br/ >5. Patient participating or having participated in a clinical trial with another investigational drug within the last 28 days except for investigational drugs against cancer, leukemia or HIV. <br/ >6. Patients with a life expectancy judged to be less than five days <br/ >7. ALT/AST > 5 times the upper limit of normal <br/ >8. Stage 4 severe chronic kidney disease or requiring dialysis (i.e. eGFR < 30) <br/ >9. Patients not likely to complete the trial as per judgment of the investigator.

1. Pregnant or nursing female. <br/ >2. Patients with history of allergy, hypersensitivity, or any serious reaction to study medication <br/ >3. Patients with a concomitant medical condition, whose participation, in the opinion of the investigator, may create an unacceptable additional risk. <br/ >4. Patient previously enrolled into this study. <br/ >5. Patient participating or having participated in a clinical trial with another investigational drug within the last 28 days except for investigational drugs against cancer, leukemia or HIV. <br/ >6. Patients with a life expectancy judged to be less than five days <br/ >7. ALT/AST > 5 times the upper limit of normal <br/ >8. Stage 4 severe chronic kidney disease or requiring dialysis (i.e. eGFR < 30) <br/ >9. Patients not likely to complete the trial as per judgment of the investigator.

Nov. 13, 2021, 5:33 p.m. oms

N/A

N/A

Oct. 26, 2020, 8:29 a.m. oms

1. Pregnant or nursing female. <br/ >2. Patients with history of allergy, hypersensitivity, or any serious reaction to study medication <br/ >3. Patients with a concomitant medical condition, whose participation, in the opinion of the investigator, may create an unacceptable additional risk. <br/ >4. Patient previously enrolled into this study. <br/ >5. Patient participating or having participated in a clinical trial with another investigational drug within the last 28 days except for investigational drugs against cancer, leukemia or HIV. <br/ >6. Patients with a life expectancy judged to be less than five days <br/ >7. ALT/AST > 5 times the upper limit of normal <br/ >8. Stage 4 severe chronic kidney disease or requiring dialysis (i.e. eGFR < 30) <br/ >9. Patients not likely to complete the trial as per judgment of the investigator.

1. Pregnant or nursing female. <br/ >2. Patients with history of allergy, hypersensitivity, or any serious reaction to study medication <br/ >3. Patients with a concomitant medical condition, whose participation, in the opinion of the investigator, may create an unacceptable additional risk. <br/ >4. Patient previously enrolled into this study. <br/ >5. Patient participating or having participated in a clinical trial with another investigational drug within the last 28 days except for investigational drugs against cancer, leukemia or HIV. <br/ >6. Patients with a life expectancy judged to be less than five days <br/ >7. ALT/AST > 5 times the upper limit of normal <br/ >8. Stage 4 severe chronic kidney disease or requiring dialysis (i.e. eGFR < 30) <br/ >9. Patients not likely to complete the trial as per judgment of the investigator.