This is a multi-center, randomized, placebo-controlled study of MR-301 administered BID IV in patients with severe TBI.
Participant: 45 patients with severe TBI who maintain GCS scores 3-8 both inclusive.
Intervention: Mr-301 or placebo will be administered intravenously BID for upto 3 weeks.
Primary Outcome: Safety and Tolerability of MR-301
Secondary Outcome: GOS-E, CRS-R, DRS, FOUR score, time to ICU discharge, time to hospital discharge and mortality.