100
Participants
Start Date
November 23, 2022
Primary Completion Date
June 30, 2026
Study Completion Date
June 30, 2026
Esperoct
Participants will be treated with commercially available Esperoct for a total study duration of 24 months according to the local label and local routine clinical practice at the discretion of the physician. The decision to switch to Esperoct will be made prior to and separate from the decision to enrol in the study.
RECRUITING
Novo Nordisk Investigational Site, Hamilton
Lead Sponsor
Novo Nordisk A/S
INDUSTRY