HAYA Therapeutics is a precision therapeutics company that discovers and develops innovative tissue- and cell-selective genomic medicines for fibrotic diseases and other serious health conditions associated with aging, including cancer. The company’s discovery engine focuses on long non-coding RNAs (lncRNAs) within the “dark matter” of the human genome -- key tissue and cell-specific drivers of fibrosis and other disease processes -- to identify novel targets and drug candidates with the potential for greater efficacy and safety than existing treatments.

AceLink Therapeutics is a clinical-stage biopharma company with a focus on kidney diseases and genetic diseases with unmet clinical needs. Founded in 2018, AceLink is headquartered in San Francisco Bay area and has discovery and clinical development operations in US and Chuina. Our leading drug candidate AL01211 is a GCS inhibitor that offers a novel therapeutic approach for Fabry disease and other kidney diseases. AL01211 has successfully completed Ph1 clinical trial and is expected to enter phase 2 trial in patients with Fabry disease in 2022. The second drug program offers new treatment options for several neuropathic and neurodegenerative diseases. In addition to the above, our drug pipeline combines internal drug discovery, led by experienced drug development scientists, and licensing in external assets. AceLink has finished two rounds of VC fundraising.

QurAlis is bringing hope to the ALS community by developing breakthrough precision medicines for this devastating disease. Quralis' stem cell technologies generate proprietary human neuronal models that enable them to more effectively discover and develop innovative therapies for genetically validated targets. They are advancing three antisense and small molecule programs addressing sub-forms of the disease that account for the majority of patients.