Arrowhead Pharmaceuticals Earns $20 Million Milestone Payment from Amgen for Start of Phase 2 Trial of AMG 890
The clinical study (NCT04270760) is a double-blind, randomized, placebo-controlled Phase 2 study to evaluate efficacy, safety, and tolerability of AMG 890 in 240 subjects with elevated Lp(a). The primary outcome measure is the percent change in Lp(a) from baseline to week 36. Secondary outcome measures include the percent change in Lp(a) from baseline to week 48, percent change in low-density lipoprotein cholesterol (LDL-C) from baseline to weeks 36 and 48, percent change in Apolipoprotein(B) (ApoB) from baseline to weeks 36 and 48, maximum observed concentration (Cmax) of AMG 890, and area under the concentration-time curve (AUC).
Under the terms of the agreement with Amgen announced in
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