drugset / Trial / NCT04498650
A Study to Evaluate Safety and Tolerability of Different Doses and Efficacy of PQ912 in Subjects With MCI and Mild AD
Phase 2
Completed
259 enrolled
Vivoryon Therapeutics N.V.
Amsterdam UMC, location VUmc · collabNordic Bioscience A/S · collab
RandomizedParallel-groupTriple-blindTreatment
Summary
This is a phase 2B multicenter, randomized, double-blind, placebo-controlled, parallel group dose finding study to evaluate the safety, tolerability and efficacy of PQ912, an inhibitor of the glutaminyl cyclase enzyme, in 250 subjects with mild cognitive impairment and mild dementia due to Alzheimer 's Disease.
Timeline
- Start
- 2020-07-06
- Primary completion
- 2023-12-18
- Completion
- 2024-01-12
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | PQ912 | Small molecule | 300 mg | Oral |
| Subject | PQ912 | Small molecule | 600 mg | Oral |