ADD-VANTAGE

A randomized, double-blind, placebo-controlled, multicenter study to evaluate the efficacy, safety, and tolerability of pelacarsen (TQJ230) with background inclisiran in participants with atherosclerotic cardiovascular disease, and elevated LDL-C and Lp(a)

Stage
inclusie
Medicine
Pelacarsan (en inclisiran)
Population
ASCVD
Phase
III
First Patient In
28 February 2026
Last Patient In
1 October 2026
Last Patient Last Visit
16 October 2027

Inclusion period, 203 days remaining

Office Contact

M.J. van Doorn

WCN

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