A Randomised, Double-blind, Placebo-controlled Single and Multiple Ascending Dose Study in Healthy Volunteers and Asymptomatic GRN Mutation Carriers to Investigate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of VES001
Latest Information Update: 05 Sep 2024
At a glance
- Drugs VES 001 (Primary)
- Indications Frontotemporal dementia
- Focus Adverse reactions; First in man
Most Recent Events
- 04 Sep 2024 Results presented in a Vesper Bio Media Release.
- 22 Aug 2024 Status changed from recruiting to completed.
- 30 May 2024 Results published in a Vesper Bio media release