1. in the opinion of the investigator, unlikely to survive for \>48 hours from screening. 2. any physical examination findings and/or history of any illness that, in the opinion of the study investigator, might confound the results of the study or pose an additional risk to the patient by their participation in the study. 3. currently receiving extracorporeal membrane oxygenation (ecmo) or high frequency oscillatory ventilation (hfov). 4. females who are pregnant. 5. patients with active bacteremia at start of therapy enrollment or concurrently active moderate to severe other infectious which in the opinion of the investigator may possibly affect the safety of ck0802 treatment. 6. patients who have been intubated for more than 120 hours. 7. known hypersensitivity to dmso or to porcine or bovine protein. 8. any end-stage organ disease which in the opinion of the investigator may possibly affect the safety of ck0802 treatment. 9. high dose steroids. 10. receiving an investigational cellular therapy agent.

1. in the opinion of the investigator, unlikely to survive for \>48 hours from screening. 2. any physical examination findings and/or history of any illness that, in the opinion of the study investigator, might confound the results of the study or pose an additional risk to the patient by their participation in the study. 3. currently receiving extracorporeal membrane oxygenation (ecmo) or high frequency oscillatory ventilation (hfov). 4. females who are pregnant. 5. patients with active bacteremia at start of therapy enrollment or concurrently active moderate to severe other infectious which in the opinion of the investigator may possibly affect the safety of ck0802 treatment. 6. patients who have been intubated for more than 120 hours. 7. known hypersensitivity to dmso or to porcine or bovine protein. 8. any end-stage organ disease which in the opinion of the investigator may possibly affect the safety of ck0802 treatment. 9. high dose steroids. 10. receiving an investigational cellular therapy agent.

in the opinion of the investigator, unlikely to survive for >48 hours from screening. any physical examination findings and/or history of any illness that, in the opinion of the study investigator, might confound the results of the study or pose an additional risk to the patient by their participation in the study. currently receiving extracorporeal membrane oxygenation (ecmo) or high frequency oscillatory ventilation (hfov). females who are pregnant. patients with active bacteremia at start of therapy enrollment or concurrently active moderate to severe other infectious which in the opinion of the investigator may possibly affect the safety of ck0802 treatment. patients who have been intubated for more than 120 hours. known hypersensitivity to dmso or to porcine or bovine protein. any end-stage organ disease which in the opinion of the investigator may possibly affect the safety of ck0802 treatment. high dose steroids. receiving an investigational cellular therapy agent.

in the opinion of the investigator, unlikely to survive for >48 hours from screening. any physical examination findings and/or history of any illness that, in the opinion of the study investigator, might confound the results of the study or pose an additional risk to the patient by their participation in the study. currently receiving extracorporeal membrane oxygenation (ecmo) or high frequency oscillatory ventilation (hfov). females who are pregnant. patients with active bacteremia at start of therapy enrollment or concurrently active moderate to severe other infectious which in the opinion of the investigator may possibly affect the safety of ck0802 treatment. patients who have been intubated for more than 120 hours. known hypersensitivity to dmso or to porcine or bovine protein. any end-stage organ disease which in the opinion of the investigator may possibly affect the safety of ck0802 treatment. high dose steroids. receiving an investigational cellular therapy agent.

1. in the opinion of the investigator, unlikely to survive for >48 hours from screening. 2. any physical examination findings and/or history of any illness that, in the opinion of the study investigator, might confound the results of the study or pose an additional risk to the patient by their participation in the study. 3. currently receiving extracorporeal membrane oxygenation (ecmo) or high frequency oscillatory ventilation (hfov). 4. females who are pregnant. 5. patients with active bacteremia at start of therapy enrollment or concurrently active moderate to severe other infectious which in the opinion of the investigator may possibly affect the safety of ck0802 treatment. 6. patients who have been intubated for more than 120 hours. 7. known hypersensitivity to dmso or to porcine or bovine protein. 8. any end-stage organ disease which in the opinion of the investigator may possibly affect the safety of ck0802 treatment. 9. high dose steroids. 10. receiving an investigational cellular therapy agent.

1. in the opinion of the investigator, unlikely to survive for >48 hours from screening. 2. any physical examination findings and/or history of any illness that, in the opinion of the study investigator, might confound the results of the study or pose an additional risk to the patient by their participation in the study. 3. currently receiving extracorporeal membrane oxygenation (ecmo) or high frequency oscillatory ventilation (hfov). 4. females who are pregnant. 5. patients with active bacteremia at start of therapy enrollment or concurrently active moderate to severe other infectious which in the opinion of the investigator may possibly affect the safety of ck0802 treatment. 6. patients who have been intubated for more than 120 hours. 7. known hypersensitivity to dmso or to porcine or bovine protein. 8. any end-stage organ disease which in the opinion of the investigator may possibly affect the safety of ck0802 treatment. 9. high dose steroids. 10. receiving an investigational cellular therapy agent.