drugset / Trial / NCT02248116

Follow-up Trial to Assess the Long-term Safety and Tolerability of Talsaclidine in Patients With Mild to Moderate Dementia of the Alzheimer Type

NCT02248116

Phase 2/3 Terminated 198 enrolled Boehringer Ingelheim
NaSingle-groupOpen-labelTreatment

Summary

Safety and tolerability. Quality of life (EQ-5D, ACQLI) and health economic impact (health resource utilisation, living and employment status) assessments, will not be performed at the centers in the united kingdom (UK)

Timeline

Start
1999-05
Primary completion
2000-09
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Talsaclidine Small molecule 24 mg Oral

Indications