drugset / Trial / NCT01303744

Evaluation of Safety & Tolerability of Multiple Dose Regimens of CHF 5074

NCT01303744 ↗

Phase 2 Completed 96 enrolled CERESPIR
RandomizedParallel-groupQuadruple-blindTreatment

Summary

To evaluate the safety and tolerability of ascending oral doses of CHF 5074 administered once per day for up to 12 weeks to patients with mild cognitive impairment.

Timeline

Start
2011-03
Primary completion
2012-04
Completion
2012-04

Drugs

EvaluationDrugModalityDoseRoute
Subject CHF 5074 Unknown — Oral

Indications