BENITIONSClinical Trial Intelligence

A Multicenter Trial Assessing the Impact of Lipoprotein(a) Lowering With Pelacarsen (TQJ230) on the Rate of Weekly Lipoprotein Apheresis Sessions in Patients With Hyperlipoproteinemia(a) and Established Cardiovascular Disease in Germany

第3相 完了 NCT05305664

対象疾患Hyperlipoproteinemia
第3相
スポンサーNovartis Pharmaceuticals
ステータス完了
参加者数51 名
介入(薬剤)Pelacarsen (TQJ230) 80 mg s.c., Corresponding Placebo
開始日2022年8月19日
完了日2025年1月28日
結果公開日2026年7月17日

概要

Phase III study to test the hypothesis that treatment with pelacarsen (TQJ230) 80 mg Q4W compared to placebo significantly reduces the rate of lipoprotein apheresis in patients with hyperlipoproteinemia (a) and established cardiovascular disease currently undergoing lipoprotein apheresis in Germany on a weekly schedule.

Rate of Lipoprotein Apheresis Sessions Performed Over 52 Weeks Normalized to the Weekly Lipoprotein Apheresis Schedule

Up to Week 52 · Apheresis sessions received per week

Pelacarsen (TQJ230)0.16 Apheresis sessions received per week
Placebo0.93 Apheresis sessions received per week
p-value<0.0001
Odds Ratio (OR)0.006 (95% CI 0.003–0.013)

BENITIONS で見る ClinicalTrials.gov の原文を見る

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