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Trial · NCT01879319

Study to Assess in Home Use of Evolocumab (AMG 145) Administration Using Either an Automated Mini-doser or a Prefilled Autoinjector/Pen

NCT01879319, Phase 3, Completed, Amgen; results first posted 2015-12-23

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Study to Assess in Home Use of Evolocumab (AMG 145) Administration Using Either an Automated Mini-doser or a Prefilled Autoinjector/Pen. Trials, record NCT01879319. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT01879319

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Study to Assess in Home Use of Evolocumab (AMG 145) Administration Using Either an Automated Mini-doser or a Prefilled Autoinjector/Pen
NCT number
NCT01879319
Status
Completed
Phases
Phase 3
Enrollment
164 participants, actual
Lead sponsor
Amgen
Conditions
Primary Hypercholesterolemia, Mixed Dyslipidemia
Interventions
Evolocumab AMD, Evolocumab AI/pen
First posted
2013-06-17
Last updated
2022-11-30
Results first posted
2015-12-23

Source ClinicalTrials.gov

Registered outcomes2

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryPercentage of Participants With Full Administration of Evolocumab at Both Weeks 4 and 8Weeks 4 and 8
Self-administration of evolocumab was assessed by a telephone interview at Weeks 4 and 8. Each participant was asked about all attempted injection(s) and if the injection was administered in part, full, or none at all. Results only include full administrations that occurred inside the prespecified visit window.
SecondaryPercent Change From Baseline in LDL-C at the Mean of Weeks 10 and 12Baseline and Weeks 10 and 12

Outcomes2

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYPercentage of Participants With Full Administration of Evolocumab at Both Weeks 4 and 8Weeks 4 and 8Full analysis setPercentage of participantsNUMBER
SECONDARYPercent Change From Baseline in LDL-C at the Mean of Weeks 10 and 12Baseline and Weeks 10 and 12Full analysis setpercent changeLEAST_SQUARES_MEAN

Results by group4

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Percentage of Participants With Full Administration of Evolocumab at Both Weeks 4 and 8Evolocumab AMD93.995% Confidence Interval 86.5 to 97.4Percentage of participants
Percentage of Participants With Full Administration of Evolocumab at Both Weeks 4 and 8Evolocumab AI/Pen91.595% Confidence Interval 83.4 to 95.8Percentage of participants
Percent Change From Baseline in LDL-C at the Mean of Weeks 10 and 12Evolocumab AMD-67.9Standard Error 2.4percent change
Percent Change From Baseline in LDL-C at the Mean of Weeks 10 and 12Evolocumab AI/Pen-64.5Standard Error 2.4percent change

Participant flow8

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDEvolocumab AMD82
Overall StudySTARTEDEvolocumab AI/Pen82
Overall StudyReceived TreatmentEvolocumab AMD82
Overall StudyReceived TreatmentEvolocumab AI/Pen82
Overall StudyCOMPLETEDEvolocumab AMD80
Overall StudyCOMPLETEDEvolocumab AI/Pen77
Overall StudyNOT COMPLETEDEvolocumab AMD2
Overall StudyNOT COMPLETEDEvolocumab AI/Pen5

Adverse events2

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEvents
seriousDeep vein thrombosisVascular disordersEvolocumab AMD082
seriousDeep vein thrombosisVascular disordersEvolocumab AI/Pen182

Adverse event totals6

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityEvolocumab AMD
Total, all-cause mortalityEvolocumab AI/Pen
Total, other adverse eventsEvolocumab AMD082
Total, other adverse eventsEvolocumab AI/Pen082
Total, serious adverse eventsEvolocumab AMD082
Total, serious adverse eventsEvolocumab AI/Pen182

Papers4

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
28249876BACKGROUNDPubMed
28717862BACKGROUNDPubMed
29353350BACKGROUNDPubMed
32114889BACKGROUNDPubMed

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons1

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

Comparison
Evolocumab AMD vs Evolocumab AI/Pen: serious adverse events

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT01879319

GET https://conductscience.org/api/trials/v1/NCT01879319/registered