Drug Pipeline

8 drugs associated with Juvenile neuronal ceroid lipofuscinosis (CLN3 disease)

DrugPhaseSponsor
AAV9/CLN7
Phase 1Benjamin Greenberg
HuCNS-SC
Phase 1StemCells, Inc.
CLN3
phase1_2Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
High dose CLN-301
Phase 2Alcyone Therapeutics, Inc
Low dose CLN-301
Phase 2Alcyone Therapeutics, Inc
Mycophenolate mofetil

The active metabolite of mycophenolate, mycophenolic acid, prevents T-cell and B-cell proliferation and the production of cytotoxic T-cells and antibodies. Lymphocyte and monocyte adhesion to endothelial cells of blood vessels that normally part of inflammation is prevented via the glycosylation of cell adhesion molecules by MPA. MPA inhibits de novo purine biosynthesis (that promotes immune cell proliferation) by inhibiting inosine 5’-monophosphate dehydrogenase enzyme (IMPDH), with a preferent

Phase 2University of Rochester
PLX-200

Macrophage colony stimulating factor receptor inhibitor; Nerve growth factor receptor Trk-A inhibitor; Neurotrophic tyrosine kinase receptor type 2 inhibitor; NT-3 growth factor receptor inhibitor

Phase 3Polaryx Therapeutics, Inc.
Cerliponase Alfa

CLN2 disease is a neurodegenerative disease caused by deficiency of the lysosomal enzyme tripeptidyl peptidase-1 (TPP1), which catabolizes polypeptides in the CNS. TPP1 has no known substrate specificity. Deficiency in TPP1 activity results in the accumulation of lysosomal storage materials normally metabolized by this enzyme in the central nervous system (CNS), leading to progressive decline in motor function. Cerliponase alfa (rhTTP1), a proenzyme, is taken up by target cells in the CNS and is

unknownBioMarin Pharmaceutical