Tellus Therapeutics
Tellus Therapeutics is a neonatal care company dedicated to developing treatments for preterm infants at risk for white matter injury (WMI). Founded in 2018, it is translating breakthrough science from Duke University, focusing on compounds found in breast milk that promote myelination and repair of brain injury. The company's mission is to improve neurodevelopmental outcomes for vulnerable newborns, with a pipeline that includes TT-20, a lead candidate for WMI treatment, and other pipeline programs. Tellus is pioneering neonatal drug development pathways and aims to provide safe, effective therapies for unmet needs in neonatal care.
Industries
Nr. of Employees
small (1-50)
Tellus Therapeutics
Products
Lead neonatal therapeutic candidate for white matter (myelin) injury (preclinical)
A lipid-derived small-molecule candidate identified from human maternal breast milk designed to promote oligodendrocyte differentiation and restore myelination after perinatal white matter injury; being advanced through IND-enabling studies and formulation for IV neonatal use.
Pipeline compound identification program
Ongoing program to identify and advance additional compounds for indications relevant to neonatal intensive care beyond white matter injury.
Lead neonatal therapeutic candidate for white matter (myelin) injury (preclinical)
A lipid-derived small-molecule candidate identified from human maternal breast milk designed to promote oligodendrocyte differentiation and restore myelination after perinatal white matter injury; being advanced through IND-enabling studies and formulation for IV neonatal use.
Pipeline compound identification program
Ongoing program to identify and advance additional compounds for indications relevant to neonatal intensive care beyond white matter injury.
Services
Preclinical development programs for neonatal therapeutics
Execution of discovery, in vivo efficacy, PK and formulation studies to advance neonatal therapeutic candidates toward IND submission.
Regulatory strategy and IND-enabling support for First-in-Neonate programs
Preparation for and engagement with regulatory authorities (pre-IND) and pursuit of pediatric-oriented regulatory designations to facilitate neonatal clinical development.
Preclinical development programs for neonatal therapeutics
Execution of discovery, in vivo efficacy, PK and formulation studies to advance neonatal therapeutic candidates toward IND submission.
Regulatory strategy and IND-enabling support for First-in-Neonate programs
Preparation for and engagement with regulatory authorities (pre-IND) and pursuit of pediatric-oriented regulatory designations to facilitate neonatal clinical development.
Expertise Areas
- Neonatal clinical trial design and strategy
- Preclinical in vivo models of neonatal white matter injury
- Discovery of natural product–derived small molecules
- Formulation development for intravenous neonatal administration
Key Technologies
- Lipid-based small molecule therapeutics
- Oligodendrocyte/ myelination biology assays
- Neonatal rodent models of white matter injury
- Preclinical pharmacokinetics (PK) studies