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RecruitingNCT04533464Updated May 24, 2024

MultiStem® for Treatment of Trauma Induced Multiple Organ Failure/Systemic Inflammatory Response Syndrome

A Phase 2 interventional study of MultiStem and Placebo in Trauma and Adult Stem Cells, sponsored by Healios K.K.. Recruiting at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2024-05-24.

Sponsored by Healios K.K. · Phase 2, Interventional, and Treatment

Phase
Phase 2
Study type
Interventional
Enrollment
156
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

Single center, prospective, randomized, double-blind, pragmatic Phase 2 clinical study in severely injured trauma patients within hours of hospitalization who have survived initial resuscitation.

02

Conditions studied

03

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. 18 years of age or older AND
  2. Received at least 3 units of any blood product in any hour before Shock Trauma Intensive Care Unit (STICU) arrival AND
  3. Survived to initial ICU arrival AND
  4. Initial hemostasis has been achieved, in the opinion of the attending surgeon AND
  5. Predicted to survive at least 24 hours after STICU arrival by the attending physician AND
  6. Ability to start and complete investigational product infusion within 24 hours after known or estimated time of injury.

Exclusion criteria

Exclusion Criteria:

  1. Prisoners, defined as those who have been directly admitted from a correctional facility.

    Prisoners are excluded because of their vulnerable population status. A free-living individual who is under police observation as a suspect will remain in the study until discharge or incarcerated.

  2. Pregnant and lactating females. It is unknown how stem cells affect a developing fetus or if they can be found in milk. To protect the safety of developing fetuses and breastfeeding children, pregnant and lactating women will be excluded.
  3. Have a head injury deemed non-survivable by the trauma or neurosurgery attending. The attending physician may determine futility from a range of injuries/physiological responses. These may include non-survivable TBI (malignant ICP elevation despite maximal therapy with findings of uncal herniation and/or brain dead exam; atlantooccipital dissociation), cardio-pulmonary failure refractory to resuscitation and those patients with an advanced directive that declines resuscitative or organ support therapies.
  4. Hemodynamically unstable or requiring clinically meaningful escalation of vasopressor dose for blood pressure support (to maintain SBP ≥ 90 mmHg) during the 30 minute period prior to study product thawing/preparation. Clinically meaningful vasopressor dose adjustment defined as ≥ 5 mcg/min increase in norepinephrine dose; ≥ 50 mcg/min increase in phenylephrine dose; ≥ 5 mcg/kg/min increase in dopamine dose; and ≥ 0.05 mcg/kg/min increase in epinephrine dose. If the patient is on vasopressin, investigators will be instructed not to titrate the vasopressin dose during this 30 minute period.
  5. Greater than 20% total body surface area burns and/or suspected inhalation injury.

    Subjects with large and severe thermal injuries and inhalation injures require a resuscitation approach that is different from current isolated trauma resuscitation strategies. Additionally, in the absence of concomitant severe blunt trauma, these subjects are unlikely to receive blood products in the early resuscitative phase.

  6. Preexisting chronic kidney disease, defined by prior documented glomerular filtration rate less than 60 mL/min/1.73m2 for 3 months or more. Patients who are unable to communicate their pre-existing conditions will be excluded by Medical Alert bracelets/IDs, stigmata pathognomonic for chronic kidney disease such as presence of dialysis vascular access devices or shunts/markedly elevated BUN/Creatinine, or abdominal incisions consistent with organ transplantation, etc.
  7. Preexisting chronic liver disease, evidenced by clinical or laboratory examinations consistent with chronic liver disease/failure (Childs A-C), patient or family report, Medical Alert bracelets/IDs or abdominal incisions consistent with organ transplantation, etc.
  8. Known condition of single kidney or concurrent use of potentially nephrotoxic medications at doses likely to be nephrotoxic
  9. Known immunodeficient condition or concurrent use of potentially immunosuppressive medications at doses likely to result in an immunosuppressed status
  10. Known allergy to MultiStem, dimethyl sulfoxide or human serum albumin
  11. No available intravenous access (peripheral or central) of at least 22-guage that can be utilized exclusively for investigational product during the time of planned infusion
  12. Clinical condition would be anticipated to deteriorate with intravenous administration of 250 ml of crystalloid
  13. Known Do Not Resuscitate (DNR) prior to randomization
  14. Enrolled in a concurrent ongoing interventional clinical trial
  15. Known functional asplenia or prior surgical removal of the spleen, or a trauma related splenic injury sufficient to precluding enrollment as determined by the PI or Co- Investigators. (trauma related splenic injuries include surgical total splenectomy or nonoperative management of AAST grade V splenic injury including splenic arterial embolization.* *Proximal splenic arterial embolization to control bleeding that leaves the spleen in situ and perfused (below Grade V) does not necessarily exclude the patient. Further, achieving Grade V, with an upgraded score due to a secondary small laceration, etc. away from primary injury will be considered a Grade IV for the purposes of the protocol.
04

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
156 participants (estimated)

Study arms

  • Experimental
    MultiStem

    Biological: MultiStem

  • Placebo comparator
    Placebo

    Biological: Placebo

Interventions

  • BiologicalMultiStem

    Intravenous Infusion

  • BiologicalPlacebo

    Intravenous Infusion

05

What researchers measure

Primary outcomes

  1. A composite of the highest Acute Kidney Injury stage (based on KDIGO guidelines)

    Time frame: Day 30

Secondary outcomes

  1. Mortality

    mortality including median time to death within the acute hospitalization period

    Time frame: Day 30, Day 90, Day 365

  2. Incidence of Acute Kidney Injury adjusted for the competing risk of death

    Time frame: Day 30

  3. Incidence of sepsis, Acute Respiratory Distress Syndrome, Multiple Organ Failure, and Venous Thromboembolism

    Time frame: Day 30

  4. Hospital days

    Free days will be defined as the number of days an individual was alive and not in the hospital.

    Time frame: Day 30

  5. ICU days

    Free days will be defined as the number of days an individual was alive and not in the ICU.

    Time frame: Day 30

  6. ventilator-free days

    Free days will be defined as the number of days an individual was alive and not on the ventilator.

    Time frame: Day 30

06

Study locations

1 of 1 sites recruiting
07

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT04533464
Lead sponsor
Healios K.K.
Collaborators
Memorial Hermann Hospital, United States Department of Defense
Responsible party
Sponsor
First posted
Aug 31, 2020
Start date
Nov 9, 2020
Primary completion
Dec 2025 (estimated)
Completion
Dec 2025 (estimated)
Last update
May 24, 2024

Study contacts

Charles Cox, MD
Contact
Charles.S.Cox@uth.tmc.edu
713-500-7300
Jeanette Podbielski, RN
Contact
Jeanette.M.Podbielski@uth.tmc.edu
713-500-6407
Charles Cox, MD
principal investigator · The University of Texas Health Science Center, Houston

Oversight

Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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