N-tert-(Butyl)hydroxylamine (NtBuHA) for Infantile Neuronal Ceroid Lipofuscinosis / CLN1 Batten Disease
preclinicalDevelop NtBuHA as a therapeutic agent for treating Infantile Neuronal Ceroid Lipofuscinosis, also referred to in the supplied company context as CLN1 Batten Disease.
Therapeutic development program supported by an NIH SBIR Phase I grant; intervention is N-tert-(Butyl)hydroxylamine.
NIH SBIR Phase I project 1R43NS100233-01 ran from 2017-03-01 to 2017-11-30 with total cost of $198,790.