Drug Pipeline
8 drugs associated with Juvenile neuronal ceroid lipofuscinosis (CLN3 disease)
| Drug | Phase | Sponsor | |
|---|---|---|---|
AAV9/CLN7 | Phase 1 | Benjamin Greenberg | ↗ |
HuCNS-SC | Phase 1 | StemCells, Inc. | ↗ |
CLN3 | phase1_2 | Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) | ↗ |
High dose CLN-301 | Phase 2 | Alcyone Therapeutics, Inc | ↗ |
Low dose CLN-301 | Phase 2 | Alcyone 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 2 | University 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 3 | Polaryx 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 | unknown | BioMarin Pharmaceutical | ↗ |