Basic Information

Gene symbol LPA Synonyms AK38, APOA, LP Type of gene protein-coding
Gene perturbation-related omics dataset PerturbAtlas
Description lipoprotein(a)

GTO ID GTC0518
Trial ID NCT04270760
Disease Cardiovascular System Disease
Altered gene LPA
Therapeutic/Target gene Target gene
TherapysiRNA
Treatment Olpasiran|AMG 890
PhasePhase2
Recruitment statusCompleted
TitleA Double-blind, Randomized, Placebo-controlled Phase 2 Study to Evaluate Efficacy, Safety, and Tolerability of Olpasiran (AMG 890) in Subjects With Elevated Lipoprotein(a)
Year2020
CountryAustralia|Canada|Denmark|Iceland|Japan|Netherlands|United States
Company sponsorAmgen
Other ID(s)20180109|2019-003688-23

Clinical Result

Cohort1: olpasiran_dose level 1
Administration route subcutaneous injection
Dosage olpasiran, 10 mg, Q12W for 48 weeks
Pts 58
Age Adult, Older_Adult
Outcome Percentage Change From Baseline in Lipoprotein(a) (Lp[a]) at Week 36:-66.91
Adverse reactions 0/58(All-cause mortality); 3/58(Cardiac disorders; Infections and infestations; Injury, poisoning and procedural complications; Product Issues)
References PMID: 36342163
Cohort2: olpasiran_dose level 2
Administration route subcutaneous injection
Dosage olpasiran, 75 mg, Q12W for 48 weeks
Pts 58
Age Adult, Older_Adult
Outcome Percentage Change From Baseline in Lipoprotein(a) (Lp[a]) at Week 36:-93.78
Adverse reactions 0/58(All-cause mortality); 3/58(Infections and infestations; Injury, poisoning and procedural complications; Musculoskeletal and connective tissue disorders; Renal and urinary disorders)
References PMID: 36342163
Cohort3: olpasiran_dose level 3
Administration route subcutaneous injection
Dosage olpasiran, 225 mg, Q12W for 48 weeks
Pts 56
Age Adult, Older_Adult
Outcome Percentage Change From Baseline in Lipoprotein(a) (Lp[a]) at Week 36:-97.53
Adverse reactions 0/56(All-cause mortality); 6/56(Cardiac disorders; astrointestinal disorders; General disorders; Metabolism and nutrition disorders; Musculoskeletal and connective tissue disorders; Neoplasms benign, malignant and unspecified(incl cysts and polyps); Respiratory, thoracic and mediastinal disorders; Skin and subcutaneous tissue disorders; Vascular disorders)
References PMID: 36342163
Cohort4: olpasiran_dose level 4
Administration route subcutaneous injection
Dosage olpasiran, 225 mg, Q24W for 48 weeks
Pts 55
Age Adult, Older_Adult
Outcome Percentage Change From Baseline in Lipoprotein(a) (Lp[a]) at Week 36:-96.89
Adverse reactions 0/55(All-cause mortality); 4/55(Cardiac disorders; General disorders; Infections and infestations; Nervous system disorders; Skin and subcutaneous tissue disorders)
References PMID: 36342163
Cohort5: Placebo
Administration route subcutaneous injection
Dosage Placebo, Q12W for 48 weeks
Pts 54
Age Adult, Older_Adult
Outcome Percentage Change From Baseline in Lipoprotein(a) (Lp[a]) at Week 36:3.60
Adverse reactions 1/54(All-cause mortality); 8/54(Cardiac disorders; General disorders; Infections and infestations; Neoplasms benign, malignant and unspecified(incl cysts and polyps); Nervous system disorders; Vascular disorders)
References PMID: 36342163
Cohort6: Extended Safety Follow Cohort1
Administration route subcutaneous injection
Pts 57
Age Adult, Older_Adult
Adverse reactions 0/57(All-cause mortality); 4/57(Cardiac disorders; Eye disorders; Gastrointestinal disorders; Nervous system disorders)
References PMID: 36342163
Cohort7: Extended Safety Follow Cohort2
Administration route subcutaneous injection
Pts 57
Age Adult, Older_Adult
Adverse reactions 0/57(All-cause mortality); 2/57(Infections and infestations; Injury, poisoning and procedural complications)
References PMID: 36342163
Cohort8: Extended Safety Follow Cohort3
Administration route subcutaneous injection
Pts 54
Age Adult, Older_Adult
Adverse reactions 0/54(All-cause mortality); 6/54(Gastrointestinal disorders; Infections and infestations; Musculoskeletal and connective tissue disorders; Psychiatric disorders; Vascular disorders)
References PMID: 36342163
Cohort9: Extended Safety Follow Cohort4
Administration route subcutaneous injection
Pts 55
Age Adult, Older_Adult
Adverse reactions 0/55(All-cause mortality); 5/55(Cardiac disorders; Gastrointestinal disorders; Infections and infestations)
References PMID: 36342163
Cohort10: Extended Safety Follow Cohort5
Administration route subcutaneous injection
Pts 53
Age Adult, Older_Adult
Adverse reactions 0/53(All-cause mortality); 4/53(Hepatobiliary disorders; Musculoskeletal and connective tissue disorders; Neoplasms benign, malignant and unspecified(incl cysts and polyps); Nervous system disorders)
References PMID: 36342163

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