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Trial · NCT02007252

ACZ885 for the Treatment of Abdominal Aortic Aneurysm

NCT02007252, Phase 2, Terminated, Novartis Pharmaceuticals; results first posted 2016-11-21

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. ACZ885 for the Treatment of Abdominal Aortic Aneurysm. Trials, record NCT02007252. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02007252

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Trial

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

Title
ACZ885 for the Treatment of Abdominal Aortic Aneurysm
NCT number
NCT02007252
Status
Terminated
Phases
Phase 2
Enrollment
65 participants, actual
Lead sponsor
Novartis Pharmaceuticals
Conditions
Abdominal Aortic Aneurysm (AAA)
Interventions
ACZ885, Placebo
First posted
2013-12-10
Last updated
2021-01-05
Other registries' IDs
eudract:2013-002088-25
Results first posted
2016-11-21

Source ClinicalTrials.gov

Registered outcomes1

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

ListOutcomeTime frameDescription
PrimaryChange From Baseline in Abdominal Aortic Aneurysm (AAA) Size Per Yearmonth 3, month 12
Size of the AAA was determined using an abdominal ultrasound technique at baseline, 3 months, and 12 months after treatment with study drug. Growth rate (in mm/year) was calculated from the change in AAA size compared to baseline

Outcomes1

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYChange From Baseline in Abdominal Aortic Aneurysm (AAA) Size Per Yearmonth 3, month 12
The pharmacodynamic analysis set, which included randomized participants who received at least one dose of study drug, was considered for the analysis. However, only participants with values at each time point were analyzed.
millimeter/yearLEAST_SQUARES_MEAN

Results by group4

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

OutcomeGroupCategoryValueSpreadUnits
Change From Baseline in Abdominal Aortic Aneurysm (AAA) Size Per YearACZ885Month 3 (n=23,31)0.78190% Confidence Interval -0.942 to 5.504millimeter/year
Change From Baseline in Abdominal Aortic Aneurysm (AAA) Size Per YearPlaceboMonth 3 (n=23,31)2.51990% Confidence Interval 1.030 to 4.008millimeter/year
Change From Baseline in Abdominal Aortic Aneurysm (AAA) Size Per YearACZ885Month 12 (n=20,23)2.53890% Confidence Interval 1.465 to 3.612millimeter/year
Change From Baseline in Abdominal Aortic Aneurysm (AAA) Size Per YearPlaceboMonth 12 (n=20,23)2.58190% Confidence Interval 1.612 to 3.549millimeter/year

Participant flow10

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDACZ88531
Overall StudySTARTEDPlacebo33
Overall StudySafety Analysis SetACZ88531
Overall StudySafety Analysis SetPlacebo33
Overall StudyPharmacodynamic Analysis SetACZ88531
Overall StudyPharmacodynamic Analysis SetPlacebo33
Overall StudyCOMPLETEDACZ88520
Overall StudyCOMPLETEDPlacebo22
Overall StudyNOT COMPLETEDACZ88511
Overall StudyNOT COMPLETEDPlacebo11

Adverse events168

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

TypeEventOrgan systemGroupAffectedAt riskEvents
otherAnaemiaBlood and lymphatic system disordersACZ885131
otherAnaemiaBlood and lymphatic system disordersPlacebo033
otherAngina pectorisCardiac disordersACZ885031
otherAngina pectorisCardiac disordersPlacebo233
otherAtrial fibrillationCardiac disordersACZ885231
otherAtrial fibrillationCardiac disordersPlacebo033
otherAtrioventricular block second degreeCardiac disordersACZ885031
otherAtrioventricular block second degreeCardiac disordersPlacebo133
otherCataractEye disordersACZ885031
otherCataractEye disordersPlacebo133

Adverse event totals6

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityACZ885
Total, all-cause mortalityPlacebo
Total, other adverse eventsACZ8852831
Total, other adverse eventsPlacebo2833
Total, serious adverse eventsACZ885231
Total, serious adverse eventsPlacebo033

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

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
ACZ885 vs Placebo: 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/NCT02007252

GET https://conductscience.org/api/trials/v1/NCT02007252/events?page=2