Boulder Bioscience


Privately held biotechnology company developing small-molecule drug candidates and formulation technologies to treat acute brain injuries, including acute ischemic stroke (AIS) and traumatic brain injury (TBI). The company focuses on lipid-based formulation approaches that enable oral and intravenous delivery of a brain-penetrant API, and conducts IND-enabling and translational preclinical studies to support clinical development.

Industries

N/A

Nr. of Employees

small (1-50)

Boulder Bioscience

4909 Nautilus Ct N Ste 130, Boulder, CO 80301, United States


Patents

Compositions and methods for treating non-hemorrhagic closed head injury

US-12171745-B2

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Methods for improved endovascular thrombectomy using 3,3′-diindolylmethane

US-11980604-B2

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Methods for improved endovascular thrombectomy using 3,3′-diindolylmethane

US-11529331-B2

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Products

Oral lipid-based self-micro-emulsifying formulation of a neuroprotective small molecule (field formulation)

Oral SMEDDS formulation designed to increase bioavailability of a brain-penetrant small-molecule API for pre-hospital or field administration in mild TBI/concussion and screened AIS patients; IND-enabled with completed 28-day GLP safety toxicology and PK studies in rats.

Intravenous nanoscale emulsion premix of a neuroprotective small molecule

Intravenous premix formulation that forms a nanoscale emulsion on dilution, intended for administration by emergency professionals and interventional neuro-radiologists (e.g., prior to or during thrombectomy); demonstrated pivotal efficacy in a rodent TBI contusion model.

Expertise Areas

  • Formulation and drug delivery for poorly soluble small molecules
  • Preclinical translational neuroscience (AIS and TBI)
  • Neuroinflammation and innate immune modulation
  • IND-enabling development and GLP toxicology
  • Show More (2)

Key Technologies

  • Self-micro-emulsifying drug delivery systems (SMEDDS)
  • Intravenous nanoemulsion/premix formulations
  • Small-molecule brain-penetrant APIs
  • GLP toxicology and pharmacokinetic studies
  • Show More (2)

News & Updates

Completed GLP-compliant 28-day safety toxicology and pharmacokinetic study supporting IND-enabling status for the oral formulation.

Completed pivotal efficacy study showing neuroprotection, blood–brain barrier protection, reduced cerebral edema, and improved neurocognitive outcomes for the IV formulation in a rigorous translational rodent model.

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