1 |
Discovery of PIP5Kgamma inhibitor for treatment of Parkinson's disease |
Small Molecules |
Parkinson's disease |
PIP5Kγ |
Hit |
K.MEDI hub |
RS-2023-00283494 |
|
2 |
Development of gene.editing therapeutics for Huntington’s disease with CAG repeat expansion |
Gene Therapy |
Huntington's disease |
HTT gene(CAG.repeat) |
Hit |
GenKOre |
RS-2023-00259174 |
|
3 |
Development of therapeutic agent for Parkinson's disease targeting alpha synuclein aggregates using autophagy targeting chimera (AUTOTAC) |
Small Molecules |
Parkinson's disease |
α-Syn |
Hit |
AUTOTAC Bio Inc. |
RS-2022-00166787 |
|
4 |
Developing biomedicine to overcome neuropathic pain by GCH1 expression down-regulation |
Gene Therapy |
Neuropatic Pain |
GCH1 |
Hit |
Yonsei University |
HN22C0307 |
|
5 |
Development of an exosome-mediated intracellular therapeutic protein delivery system for Parkinson's disease |
Others |
Parkinson's disease |
Parkin, PGC-1α |
Hit |
Sungkyunkwan University |
HN21C1266 |
|
6 |
Development of a lead compound for preventing Parkinson’s disease using small compounds with inhibitory mechanism of initial alpha-synuclein aggregation |
Small Molecules |
Parkinson's disease |
α-synuclein |
Hit |
Hanyang University |
HN21C1258 |
|
7 |
Bone-delivered therapeutic antibody for osteoporosis based on clinically verified, innovative mode of action |
Antibody |
Osteoporosis |
Cathepsin K |
Hit |
Ewha Women's University |
HN21C0317 |
|
8 |
Development of lead compound for treatment of hearing loss caused by cisplatin |
Small Molecules |
Hearing loss |
DRAK1, ADCK4, CDC42BPA |
Hit |
Kyungpook National University |
HN21C0107 |
|
9 |
Development of lead compounds as antidepressant having both α2 adrenergic antagonist and NDRI activities |
Small Molecules |
Major depressive disorder |
A2 adrenergic, NDRI |
Hit |
Kyung Hee University |
HN21C1076 |
|
10 |
Discovery of Lead Candidates for Parkinson’s disease targeting novel TAS2R GPCR |
Small Molecules |
Parkinson's disease |
TAS2R |
Lead |
DIGMBIO |
RS-2023-00219269 |
|
11 |
Discovery of a novel lead compound for chronic pain treatments using a TRPV1 binding peptides design and manufacture platform |
Peptide |
Chronic Pain |
TRPV1 |
Lead |
Gachon University |
RS-2022-00167087 |
|
12 |
The lead selection study of TLR2 targeted antisense oligonucleotide
using PNA as a therapeutic agent for Parkinson’s Disease (PD) |
Nucleic acid/Virus |
Parkinson's Disease |
TLR2 |
Lead |
SEASUN THERAPEUTICS, Inc. |
HN22C0411 |
|
13 |
Discovery of a lead compound utilizing exon skipping platform for the treatment of
amyotrophic lateral sclerosis |
Nucleic acid/Virus |
Amyotrophic Lateral Sclerosis |
STMN2 |
Lead |
OliPass corporation |
HN22C0017 |
|
14 |
Lead identification of ASK1 inhibitor as a therapeutic agent for Parkinson’s disease |
Small Molecules |
Parkinson's disease |
ASK1 |
Lead |
Korea Research Institute of Chemical Technology |
HN21C1139 |
|
15 |
Discovery of Lead Compounds for the Treatment of Progressive Supranuclear Palsy by Controlling 4R Tauopathy |
Small Molecules |
Progressive supranuclear palsy, 4R tauopathies |
4R tau oligomer |
Lead |
Korea Institute of Science and Technology |
HN21C0315 |
|
16 |
Development of treatment for neurodevelopmental disorder (Rett syndrome) based on RNA replacement technology using the next-generation efficacy evaluation method |
Gene Therapy |
Rett syndrome |
MeCP2 |
Lead |
Rznomics Inc. |
HN21C1329 |
|
17 |
Development of KV7.4 specific activator for the treatment of genetic hearing loss(DFNA2) |
Small Molecules |
Genetic Hearing Loss |
KV7.4 |
Lead |
Yonsei University |
HN21C0163 |
|
18 |
Development of AAV.based regenerative medicine expressing HGF gene (AAV9.HGF) for the treatment of ALS disease |
Gene Therapy |
Amyotrophic Lateral Sclerosis |
HGF/c.Met signaling pathway |
Candidate |
Helixmith Co.,Ltd. |
RS-2023-00283601 |
|
19 |
Development of therapeutic antibody for the treatment of myasthenia gravis |
Antibody |
Myasthenia gravis |
Disclosure after confidentiality agreement |
Candidate |
Medytox Inc. |
RS-2023-00283006 |
|
20 |
Development of ASO therapeutics to treat childhood intractable epilepsy |
Gene Therapy |
Pediatric epilepsy |
MTOR |
Candidate |
Sovargen Co., Ltd. |
RS-2023-00282544 |
|
21 |
Discovery the preclinical candidate for amyotrophic lateral sclerosis (ALS) based on the activation of lysosomes using small-molecular proteins |
Peptide |
Amyotrophic lateral sclerosis |
Zn2+ |
Candidate |
ZINCURE |
RS-2023-00218770 |
|
22 |
Investigation of proper candidates for in vivo direct lineage reprogramming based SCI gene therapy development |
Gene Therapy |
Spinal cord injury |
astrocyte |
Candidate |
Stand Up Therapeutics |
RS-2022-00167083 |
|
23 |
Development of small molecule LRRK2 inhibitor for Parkinson’s disease treatment |
Peptide |
Parkinson's disease |
LRRK2 |
Candidate |
Whan In Pharm. Co., Ltd. |
HN21C0655 |
|