PKN605-AF

A randomized, placebo-controlled, participant- and investigator-blinded study to evaluate the efficacy, safety, tolerability, and pharmacokinetics of oral PKN605 in participants with atrial fibrillation

Stage
inclusie
Medicine
PKN605
Population
Ritme
Phase
II
First Patient In
15 December 2025
Last Patient In
1 July 2027
Last Patient Last Visit
15 May 2028

Inclusion period, 313 days remaining

Study Director

dr. M.E.W. Hemels

Cardioloog

Office Contact

M.J. van Doorn

Studiemanager

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