drugset / Trial / NCT03398434

Efficacy and Safety of MAA868 in Patients With Atrial Fibrillation

NCT03398434 ↗

Phase 2 Withdrawn Novartis Pharmaceuticals
RandomizedParallel-groupSingle-blindBasic science

Summary

The purpose of this study is to evaluate the pharmacokinetics, pharmacodynamics, safety and tolerability of MAA868 compared to apixaban in patients with atrial fibrillation.

Timeline

Start
2018-10-16
Primary completion
2019-11-28
Completion
2020-01-30

Outcome

Outcome not reported

Stopped (Enrollment): “Trial cancelled before First Patient First Visit (no patient enrolled)”

Drugs

EvaluationDrugModalityDoseRoute
Comparator Apixaban Small molecule 5 mg —
Subject MAA868 Unknown — Subcutaneous

Indications