About this trial
Traumatic Brain Injury (TBI) is an alteration of brain function caused by an external force. Long-term mortality in TBI is substantial, TBI survivors can develop chronic progressive disabilities and have a life expectancy shortened by 6 years. Treatment consists in supportive therapy directed at prevention of second insults, but no neuroprotective therapy is available. Given the multifaceted nature of TBI, mesenchymal stromal cells (MSCs) are an ideal candidate: they release multiple soluble factors shown to ameliorate the injury microenvironment through immunomodulatory, protective, reparative and regenerative processes. Preclinical data across a range of different TBI models and injury severities show that human MSCs improve outcome through pleiotropic mechanisms of protection and repair. Thus, data indicate MSCs as strong therapeutic candidate and support a clinical study in TBI.
Aim: the study is designed to assess the safety and the efficacy of the MSCs, intravenously administered in severe TBI patients within 48h from injury. The study will be conducted in a stepwise manner. Step 1 will enroll 36 patients (randomized 1:1:1 in arms 80 x 10\^6 MSCs vs 160 x 10\^6 MSCs vs placebo) to define safety, and will allow to select the most promising dose. Step 2 will enroll 30 patients (1:1 in arms MSCs selected dose vs placebo) to define the MSC activity based on the quantification of the plasmatic levels of the neurofilament light (NFL) at 14 days, as biomarker of neuronal damage.
Secondary objectives are aimed to assess:
1. brain injury evolution and white matter damage by longitudinal neuroimaging (at 4 days and 14 days post-TBI and at 6 months) 2. brain immunomodulatory changes by temporal profiling of circulating biomarkers of brain damage and neuroinflammation (daily for 3 days after TBI, at day 7 and 14, and at 1, 6 and 12 months) 3. clinical outcome by a structured clinical and neuropsychological assessment at both 6 and 12 months
Methods: a multicenter, double blind, randomized, placebo-controlled, adaptive phase II dose finding study.
Duration of the study: 36 months (24 of enrolment and 12 of follow up).
Funding: Fondazione Regionale per la ricerca Biomedica, FRRB (Call "Unmet medical needs", proposal number 3440227) and Italian Ministry of health (Ministero della Salute, Bando di Ricerca Finalizzata 2021; proposal number RF-2021-12372642).
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Age: 18-70 years
Clinical frailty index (CFI) < 5
Evidence of TBI confirmed by abnormalities consistent with trauma on CT scan upon admission (Marshall's CT Classification >1)
Feasibility of study drug (MSC/placebo) administration within 48 hours from TBI
Disqualifiers
Motor GCS > 5 at recruitment
High likelihood (> 85%) of death in the first 48 h calculated by IMPACT calculator on early admission data
Bilateral mydriasis
Opening ICP > 40 mmHg
Trial design
Parallel
Treatments tested in this trial
Mesenchymal stromal cell low dosage-80*10^6 cells
DrugMSCs have to be administered at the dosage of 80\*10\^6. MSCs have to be administered by intravenous infusion via an in situ venous catheter within 15 minutes from the preparation and within 48 hours from TBI. They have to be diluted 1:2 in a saline solution for a total of 36mL.
Mesenchymal stromal cell low dosage-160*10^6 cells
DrugMSCs have to be administered at the dosage of 160\*10\^6. MSCs have to be administered by intravenous infusion via an in situ venous catheter within 15 minutes from the preparation and within 48 hours from TBI. They have to be diluted 1:2 in a saline solution for a total of 36mL.
Placebo-storage solution
Other interventionPlacebo has to be administered by intravenous infusion via an in situ venous catheter within 15 minutes from the preparation and within 48 hours from TBI. It has to be diluted 1:2 in a saline solution for a total of 36mL.
Treatment groups
Trial outcomes
Primary outcomes
safety of mesenchimal stromal cell intravenous administration in TBI patients
number of patients in each of the two experimental dosage group experiencing at least one serious adverse drug reaction (SADR) (assessed by CTCAE v5.0) within 14 days from treatment. The maximum number of patients experiencing at least one SADR to observe in each experimental group is 1 out of 12.
efficacy of mesenchimal stromal cells in preventing subacutely post-TBI brain axonal injury
number of MSC-treated patients who reach a plasmatic NFL (neurofilament light) increase at 14 days post-treatment equal or lower than 5-fold compared to the baseline (these patients are defined as "responder patients")
Secondary outcomes
efficacy of mesenchimal stromal cells in preventing post-TBI brain anatomical injury
number of MSC-treated patients that show an improvement in terms of atrophy, diffusion and myelin integrity detected by longitudinal advanced MRI performed acutely (at 4 days post-TBI), subacutely (at 14 days) and at 6 months post-TBI.
efficacy of mesenchimal stromal cells in preventing the plasmatic increase of TBI-related circulating biomarkers
number of patients who have decreased values of markers related to axonal damage (NFL, GFAP), neuroinflammation (IL-6, IL-10, TNFa) and vascular damage (MMP9) evaluated daily for 3 days after TBI, at day 7 and 14, and at 1, 6 and 12 months
efficacy of mesenchimal stromal cell administration in improving the clinical outcome of TBI patients
number of patients with an improved clinical and neuropsychological outcome at both 6 and 12 months evaluated by the administration of structured clinical and neuropsychological questionnaires (Glasgow Outcome Scale Extended (GOSE) and quality of life after brain injury test (QOLIBRI)).
Sponsors and contacts
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Fondazione IRCCS San Gerardo dei Tintori
Lead sponsor
Istituto Di Ricerche Farmacologiche Mario Negri
Collaborator
A.O. Ospedale Papa Giovanni XXIII
Collaborator
Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico
Collaborator