Table 3.
All the visits have a window of ± 1 day | Screening/D0 | D1–D90 or until discharge | D7 | D14 | D21 | D28 | D90 |
---|---|---|---|---|---|---|---|
Informed consent | x | ||||||
SARS-CoV-2 PCR testing | x | x | x | x | x | ||
Medical history | x | ||||||
Concomitant medications | x | x | x | x | x | x | x |
Physical examination | x | x | x | x | x | x | x |
Vital signs | x | x | x | x | x | x | x |
Respiratory status | x | x | x | x | x | x | |
Hematology | x | X3 (day 3) | x | x | x | x | |
Biochemistry | x | X3 (day 3) | x | x | x | x | |
Markers of immunological function1 | x | x | x | x | x | x | |
Blood sample for additional investigational studies | x | x | x | x | x | ||
Donor chimerism | X2 (day 3) | x | X2 | X2 | X2 | ||
Pregnancy test | x | ||||||
Scales (NEWS and 7 point scale) | x | x | x | x | x | x | x |
Evaluation of patient recovery | x | ||||||
Improvement according to the investigator/second dose** | x | ||||||
Adverse events | x |
1Performed at screening and weekly
2Days 3 and 7. If donor chimerism persists by day 7, repeat on days 14, 21, and 28 and then continue weekly (until disappearance). Stop once it is negative
3Day 3
**Those patients showing clinical improvement at day 7 according to the investigator (based on respiratory status and blood-result tests) who have not shown previous toxicities of grade 3 or higher and if donor chimerism does not persist can receive a second cycle with the same dose at day 7, if the investigator considers it appropriate
Patients will be followed until day 90, discharge, or death, whichever occurs earlier. However, if the patient is discharged before day 30, weekly ambulatory visits (days 7, 14, 21, and 28) will be performed if the investigator considers it appropriate