Drug Profile

Research programme: alfa synuclein degraders- APRINOIA Therapeutics

Alternative Names: α-Syn degraders

Latest Information Update: 12 Feb 2024

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At a glance

Orphan Drug Status

Orphan designation is assigned by a regulatory body to encourage companies to develop drugs for rare diseases.

No
New Molecular Entity Yes

12 Feb 2024 Preclinical trials in Multiple system atrophy in Taiwan (Parenteral) (APRINOIA Therapeutics Pipeline, February 2024)
07 Jul 2022 Preclinical trials in Lewy body disease in Taiwan (Parenteral) (APRINOIA Therapeutics pipeline, July 2022)
07 Jul 2022 Preclinical trials in Parkinson's disease in Taiwan (Parenteral) (APRINOIA Therapeutics pipeline, July 2022)

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