A Dose-range Finding Study of MAA868 in Patients With Atrial Fibrillation

PHASE2CompletedINTERVENTIONAL
Enrollment

28

Participants

Timeline

Start Date

December 11, 2019

Primary Completion Date

December 29, 2020

Study Completion Date

March 8, 2021

Conditions
Atrial Fibrillation
Interventions
BIOLOGICAL

MAA868 Cohort 1

Subcutaneous injection: low dose

BIOLOGICAL

MAA868 Cohort 2

Subcutaneous injection: high dose

BIOLOGICAL

MAA868 Cohort 3

Subcutaneous injection: Dose to be determined.

OTHER

Placebo

Subcutaneous injection: Placebo

Trial Locations (6)

19096

Anthos Investigative Site, Wynnewood

48912

Anthos Investigative Site, Lansing

67207

Anthos Investigative Site, Wichita

71301

Anthos Investigative Site, Alexandria

75069

Anthos Investigative Site, McKinney

90211

Anthos Investigative Site, Beverly Hills

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Covance

INDUSTRY

lead

Anthos Therapeutics, Inc.

INDUSTRY