drugset / Trial / NCT02258152
SYN120 Study to Evaluate Its Safety, Tolerability and Efficacy in Parkinson's Disease Dementia (SYNAPSE)
Phase 2
Completed
82 enrolled
Biotie Therapies Inc.
Acorda Therapeutics · collabMassachusetts General Hospital · collabMichael J. Fox Foundation for Parkinson's Research · collab
RandomizedParallel-groupTriple-blindTreatment
Summary
The purpose of this study placebo-controlled, randomized, double-blind study is to assess the safety and efficacy of SYN120 in patients with Parkinson's disease dementia (PDD) already treated with a stable dose of a cholinesterase inhibitor.
Timeline
- Start
- 2014-12-22
- Primary completion
- 2017-10-03
- Completion
- 2017-10-03
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | LANDIPIRDINE | Small molecule | 100 mg | Oral |