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Trial · NCT02578095

Acute Hip Fracture Study in Patients 65 Years or Greater

NCT02578095, Phase 2, Completed, Viking Therapeutics, Inc.; results first posted 2025-12-29

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Acute Hip Fracture Study in Patients 65 Years or Greater. Trials, record NCT02578095. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02578095

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Trial

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

Title
Acute Hip Fracture Study in Patients 65 Years or Greater
NCT number
NCT02578095
Status
Completed
Phases
Phase 2
Enrollment
108 participants, actual
Lead sponsor
Viking Therapeutics, Inc.
Conditions
Hip Fractures
Interventions
VK5211, Placebo
First posted
2015-10-16
Last updated
2025-12-29
Results first posted
2025-12-29

Source ClinicalTrials.gov

Registered outcomes1

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

ListOutcomeTime frameDescription
PrimaryEfficacy in Hip Fracture Patients Confirmed by DXA Scan.Baseline and Week12
Efficacy of VK5211 after 12 weeks of treatment by mean placebo-corrected percentage change in total body less head (TBLH) lean body mass assessed by whole body dual-energy x-ray absorptiometry scan (DXA) scan.

Outcomes1

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYEfficacy in Hip Fracture Patients Confirmed by DXA Scan.Baseline and Week12The ITT population was the primary analysis population for assessing efficacy.PBO adjusted percent changeLEAST_SQUARES_MEAN

Results by group4

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

OutcomeGroupCategoryValueSpreadUnits
Efficacy in Hip Fracture Patients Confirmed by DXA Scan.Placebo095% Confidence Interval 0 to 0PBO adjusted percent change
Efficacy in Hip Fracture Patients Confirmed by DXA Scan.VK5211- 0.5mg4.7595% Confidence Interval 1.70 to 7.80PBO adjusted percent change
Efficacy in Hip Fracture Patients Confirmed by DXA Scan.VK5211- 1.0mg7.1595% Confidence Interval 3.76 to 10.54PBO adjusted percent change
Efficacy in Hip Fracture Patients Confirmed by DXA Scan.VK5211- 2.0mg9.0895% Confidence Interval 5.55 to 12.60PBO adjusted percent change

Participant flow12

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDPlacebo28
Overall StudySTARTEDVK5211- 0.5mg29
Overall StudySTARTEDVK5211- 1.0mg26
Overall StudySTARTEDVK5211- 2.0mg25
Overall StudyCOMPLETEDPlacebo19
Overall StudyCOMPLETEDVK5211- 0.5mg22
Overall StudyCOMPLETEDVK5211- 1.0mg17
Overall StudyCOMPLETEDVK5211- 2.0mg17
Overall StudyNOT COMPLETEDPlacebo9
Overall StudyNOT COMPLETEDVK5211- 0.5mg7

Adverse events372

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

TypeEventOrgan systemGroupAffectedAt riskEvents
otherAnaemiaBlood and lymphatic system disordersPlacebo1281
otherAnaemiaBlood and lymphatic system disordersVK5211- 0.5mg0290
otherAnaemiaBlood and lymphatic system disordersVK5211- 1.0mg0260
otherAnaemiaBlood and lymphatic system disordersVK5211- 2.0mg2252
otherAtrial FibrillationCardiac disordersPlacebo0280
otherAtrial FibrillationCardiac disordersVK5211- 0.5mg1291
otherAtrial FibrillationCardiac disordersVK5211- 1.0mg0260
otherAtrial FibrillationCardiac disordersVK5211- 2.0mg0250
otherCardiac FailureCardiac disordersPlacebo0280
otherCardiac FailureCardiac disordersVK5211- 0.5mg0290

Adverse event totals12

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityPlacebo028
Total, all-cause mortalityVK5211- 0.5mg029
Total, all-cause mortalityVK5211- 1.0mg026
Total, all-cause mortalityVK5211- 2.0mg025
Total, other adverse eventsPlacebo1028
Total, other adverse eventsVK5211- 0.5mg1129
Total, other adverse eventsVK5211- 1.0mg826
Total, other adverse eventsVK5211- 2.0mg1625
Total, serious adverse eventsPlacebo428
Total, serious adverse eventsVK5211- 0.5mg229

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 comparisons0

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

None in this release.

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/NCT02578095

GET https://conductscience.org/api/trials/v1/NCT02578095/events?page=2