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

Stadium
inclusie
Middel
PKN605
Populatie
Ritme
Fase
II
First Patient In
15 december 2025
Last Patient In
15 november 2026
Last Patient Last Visit
15 augustus 2027

Inclusieperiode, nog 303 dagen over

Studiedirecteur

dr. M.E.W. Hemels

Cardioloog

Contact Kantoor

M.J. van Doorn

WCN

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