Pediatric Autologous Bone Marrow Mononuclear Cells for Severe Traumatic Brain Injury

Sponsor

The University of Texas Health Science Center, Houston (Other)

Overall Status

Completed

CT.gov ID

NCT01851083

Collaborator

National Institute of Neurological Disorders and Stroke (NINDS) (NIH)

Enrollment

Locations

Arms

86.4

Duration (Months)

23.5

Patients Per Site

0.3

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

Pediatric severe traumatic brain injury (TBI) is the leading cause of death and disability in children ages 1-14 years old. There are no effective therapies to treat secondary brain injury and the post-injury response of CNS apoptosis and neuroinflammation. This study is a follow-up trial from a previously performed Phase I trial that demonstrated the safety and potential CNS structural preservation effect of intravenous autologous bone marrow mononuclear cells (BMMNC) after severe TBI in children. (Cox, 2011) The study is designed as a prospective, randomized, placebo controlled, blinded Phase 2 safety/biological activity study. The investigators hope to determine the effect of intravenous infusion of autologous BMMNCs on brain structure and neurocognitive/functional outcomes after severe TBI in children.

Condition or Disease	Intervention/Treatment	Phase
Traumatic Brain Injury	Biological: autologous bone marrow mononuclear cells Other: Placebo Infusion	Phase 2

Detailed Description

Study Design: Multicenter, randomized, blinded, placebo controlled, Bayesian adaptive dose escalation design.

Study Intervention: Single dose administered within 48 hours from time of injury. Controls will undergo a sham harvest and receive similarly labeled/external appearance and volume of 0.9% NaCl. BMMNC's will be harvested and undergo processing under cGMP conditions to obtain 6x10^{6 cells/kg or 10x10}6 cells/kg weight. The cellular product/placebo will be infused within 48 hours of injury.

Safety Monitoring & Follow-Up: Subjects will be monitored for infusion related toxicity post-infusion through hospital discharge and follow-up return study visits. Laboratory and imaging studies will be repeated at the 1, 6, and 12-month follow-up visits. A medical safety monitor (MSM) will review blinded SAE reports following post-infusion Day 14 for each subject in real time to ensure good clinical practice and to quickly identify safety concerns. The MSM will remain blinded to the treatment assignment, unless the NINDS appointed DSMB approves unblinding.

Study Design

Study Type:

Interventional

Actual Enrollment :

47 participants

Allocation:

Randomized

Intervention Model:

Parallel Assignment

Masking:

Triple (Participant, Care Provider, Outcomes Assessor)

Primary Purpose:

Treatment

Official Title:

A Phase 2 Multicenter Trial of Pediatric Autologous Bone Marrow Mononuclear Cells (BMMNCs) for Severe Traumatic Brain Injury (TBI)

Study Start Date :

Aug 1, 2013

Actual Primary Completion Date :

Sep 16, 2020

Actual Study Completion Date :

Oct 12, 2020

Arms and Interventions

Arm	Intervention/Treatment
Experimental: autologous bone marrow mononuclear cells a bone marrow harvest will be performed, followed by a single intravenous infusion of autologous bone marrow mononuclear cells within 48 hours of injury.	Biological: autologous bone marrow mononuclear cells BMMNC infusion of either 6x10^6 cells/kg or 10x10^6 cells/kg weight. Other Names: BMMNCs
Placebo Comparator: placebo infusion a sham harvest will be performed, followed by a single intravenous placebo infusion within 48 hours of injury.	Other: Placebo Infusion Placebo infusion of 0.9% Sodium Chloride Other Names: Saline Infusion

Arm

Intervention/Treatment

Experimental: autologous bone marrow mononuclear cells

a bone marrow harvest will be performed, followed by a single intravenous infusion of autologous bone marrow mononuclear cells within 48 hours of injury.

Biological: autologous bone marrow mononuclear cells

BMMNC infusion of either 6x10^6 cells/kg or 10x10^6 cells/kg weight.

Other Names:

BMMNCs

Placebo Comparator: placebo infusion

a sham harvest will be performed, followed by a single intravenous placebo infusion within 48 hours of injury.

Other: Placebo Infusion

Placebo infusion of 0.9% Sodium Chloride

Other Names:

Saline Infusion

Outcome Measures

Primary Outcome Measures

brain white matter and gray matter structural preservation on diffusion tensor magnetic resonance imaging (DTMRI) [one year post infusion]
DTMRI quantitative indices of both macro and microscopic integrity will be evaluated and compared to DTMRI of immediate post-injury treated and non-treated controls.

Secondary Outcome Measures

CNS white matter and gray matter preservation in regions of interest and improves functional and neurocognitive deficits in children after TBI [one year post infusion]

Other Outcome Measures

Infusional toxicity safety evaluations [7 days post-infusion]
Murray Score and liver function tests

Eligibility Criteria

Criteria

Ages Eligible for Study:

5 Years to 17 Years

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Between 5 and 17 years of age on the day of injury,
Glasgow Coma Score (GCS) between 3 and 8, (best un-medicated post-resuscitation score during screening),
Ability to obtain legally authorized representative (LAR) consent, and complete the BMMNC/Sham harvest and cell/placebo infusion within 48 hours of the initial injury,
Ability to speak English or Spanish.

Exclusion Criteria:

Known history of: a. previous brain injury, b. intellectual deficiency or psychiatric condition, defined as inability to independently function in a regular classroom that may invalidate our ability to assess post-injury changes in cognition or behavior (ADHD and/or other learning disabilities are NOT an exclusion), c. neurologic impairment and/or deficit, d. seizure disorder requiring anti-convulsant therapy, e. recently treated infection, f. renal disease or altered renal function (post-resuscitation serum creatinine > 1.5 mg/dL), g. hepatic disease or altered liver function (post-resuscitation, non-contusion related SGPT > 150 μ/L and/or T. Bilirubin

1.3 mg/dL), h. cancer, i. immunosuppression as defined by WBC < 3, 000 cells/ml at admission, j. HIV+, k. chemical or ETOH dependency, l. history of child abuse, m. premature birth (<37 weeks GA/2500 grams) resulting in cognitive/physical disabilities and/or developmental delay.

Obliteration of perimesencephalic cistern on initial head CT/MRI suggesting prolonged hypoxic ischemic insult/herniation syndrome.
Initial hospital ICP > 40 mm Hg.
Hemodynamic instability at the time of screening defined as SBP <90 mmHg, ongoing fluid resuscitation and/or requirement for inotropic support to maintain MAP at or above normal for age - does not include CPP based inotropic support. IVF alone does not exclude from enrollment.
Uncorrected coagulopathy at the time of bone marrow harvest defined as INR > 1.6, PTT

38 sec; PLT< 100,000; Fibrinogen < 100 g/dL.

Unstable pelvic fractures defined as requiring early operative fixation.
Pulmonary contusions defined as a chest x-ray with non-anatomic opacification and/or PaO2:FiO2 ratio < 250 associated with the mechanism of injury.
Greater than AAST Grade 3 solid or hollow visceral injury of the abdomen and/or pelvis as diagnosed by CT or other imaging.
Spinal cord injury diagnosed by CT/MR imaging or clinical findings.
Persistent hypoxia defined as SaO2 < 94% for > 30 minutes occurring at any time from hospital admission to time of consent.
Positive pregnancy test, if applicable.
Concurrent participation in an interventional drug/device research study.
Unwillingness to return for follow-up visits.
Contraindications to MRI.
Penetrating brain injury.

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Phoenix Children's Hospital I University of Arizona	Phoenix	Arizona	United States	85006
2	The University of Texas Health Science Center at Houston	Houston	Texas	United States	77030