- Topline results from Phase 2 ASCEND trial of solengepras as a monotherapy treatment for early-stage Parkinson's to be presented
- First presentation of data from Phase 1 trial of novel KCNK13 inhibitor for CNS diseases targeting neuroinflammation
- Additional meeting presentations highlight potential of proprietary NETSseq platform to identify novel therapeutic targets for neurodegenerative diseases
Details of the oral presentation at AD/PD™ 2025 are as follows:
Title: Results of ASCEND: A Phase 2 Trial of Solengepras (CVN424) as an Investigational Monotherapy for Treatment of Early Parkinson's Disease
- Presenter: Aaron L. Ellenbogen, DO, MPH
- Session Date/Time: Tuesday, April 1, 2025, 1:15 p.m. CEST / 4:15 a.m. PT
Title: NETSseq Identifies Novel Therapeutic Targets for Neurodegenerative Diseases (#3592)
- Presenter: Sagar Vaidya, M.D., Ph.D.
- Session Date/Time: Sunday, April 6, 2025, 11:45 a.m. PT
- Presenter: Sagar Vaidya, M.D., Ph.D.
- Session Date/Time: Tuesday, April 8, 2025, 8 a.m. PT
- Presenter: Kelvin L. Chou, M.D., FAAN
- Session Date/Time: Wednesday, April 9, 2025, 8 a.m. PT
Cerevance is focused on advancing cell type-specific therapies for the treatment of neurodegenerative, psychiatric, and central nervous system-controlled metabolic disorders. Our proprietary platform, Nuclear Enriched Transcript Sort sequencing (NETSseq), allows us to identify targets that are expressed at very low levels, that are present in rare cell types, or that change over time as a disease progresses. Our most advanced investigational treatment, solengepras, is currently in Phase 3 development and has the potential to be a first-in-class, oral non-dopaminergic therapy for both motor and non-motor symptoms of Parkinson's disease. Our second investigational therapy, CVN766, is designed to be a highly selective oral antagonist of the orexin 1 receptor for the potential treatment of binge eating disorder and schizophrenia. Our third investigational treatment, CVN293, is a highly selective investigational oral inhibitor targeting potassium two pore domain channel subfamily K member 13 (KCNK13). CVN293 represents a potentially novel intervention point for neurodegenerative disorders and obesity. For more information, please visit www.cerevance.com and follow us on LinkedIn and X.
Contacts
Cerevance:
Johnna Simoes, ir@cerevance.com
Media:
April Dovorany, adovorany@realchemistry.com, +1-262-909-8739