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Trial · NCT02154347

Post-marketing Clinical Trial of KAD-1229 in Patients With Type 2 Diabetes Mellitus

NCT02154347, Phase 4, Completed, Kissei Pharmaceutical Co., Ltd.; results first posted 2019-09-06

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Post-marketing Clinical Trial of KAD-1229 in Patients With Type 2 Diabetes Mellitus. Trials, record NCT02154347. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02154347

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Trial

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

Title
Post-marketing Clinical Trial of KAD-1229 in Patients With Type 2 Diabetes Mellitus
NCT number
NCT02154347
Status
Completed
Phases
Phase 4
Enrollment
178 participants, actual
Lead sponsor
Kissei Pharmaceutical Co., Ltd.
Conditions
Type 2 Diabetes Mellitus
Interventions
KAD-1229, Placebo, Insulin
First posted
2014-06-03
Last updated
2019-09-06
Results first posted
2019-09-06

Source ClinicalTrials.gov

Registered outcomes1

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

ListOutcomeTime frameDescription
PrimaryChange From Baseline in HbA1c16 weeks

Outcomes1

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYChange From Baseline in HbA1c16 weeksfull analysis set% (value of HbA1c)MEAN

Results by group2

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

OutcomeGroupCategoryValueSpreadUnits
Change From Baseline in HbA1cPlacebo/KAD-12290.05Standard Deviation 1.04% (value of HbA1c)
Change From Baseline in HbA1cKAD-1229/KAD-1229-0.61Standard Deviation 0.87% (value of HbA1c)

Participant flow12

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

PeriodMilestoneGroupParticipantsUnits counted
Double-blind PeriodSTARTEDPlacebo/KAD-122960
Double-blind PeriodSTARTEDKAD-1229/KAD-1229118
Double-blind PeriodCOMPLETEDPlacebo/KAD-122957
Double-blind PeriodCOMPLETEDKAD-1229/KAD-1229114
Double-blind PeriodNOT COMPLETEDPlacebo/KAD-12293
Double-blind PeriodNOT COMPLETEDKAD-1229/KAD-12294
Open-label PeriodSTARTEDPlacebo/KAD-122957
Open-label PeriodSTARTEDKAD-1229/KAD-1229113
Open-label PeriodCOMPLETEDPlacebo/KAD-122950
Open-label PeriodCOMPLETEDKAD-1229/KAD-122988

Adverse events105

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

TypeEventOrgan systemGroupAffectedAt riskEvents
otherCold sweatSkin and subcutaneous tissue disordersPlacebo/KAD-1229 (Data Through Week 16)060
otherCold sweatSkin and subcutaneous tissue disordersKAD-1229/KAD-1229 (Data Through Week 16)2118
otherCold sweatSkin and subcutaneous tissue disordersKAD-1229 (Data Through Week 52)9175
otherHungerGeneral disordersPlacebo/KAD-1229 (Data Through Week 16)160
otherHungerGeneral disordersKAD-1229/KAD-1229 (Data Through Week 16)2118
otherHungerGeneral disordersKAD-1229 (Data Through Week 52)9175
otherAstheniaGeneral disordersPlacebo/KAD-1229 (Data Through Week 16)260
otherAstheniaGeneral disordersKAD-1229/KAD-1229 (Data Through Week 16)2118
otherAstheniaGeneral disordersKAD-1229 (Data Through Week 52)8175
otherDizzinessNervous system disordersPlacebo/KAD-1229 (Data Through Week 16)160

Adverse event totals9

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityPlacebo/KAD-1229 (Data Through Week 16)060
Total, all-cause mortalityKAD-1229/KAD-1229 (Data Through Week 16)0118
Total, all-cause mortalityKAD-1229 (Data Through Week 52)0175
Total, other adverse eventsPlacebo/KAD-1229 (Data Through Week 16)1960
Total, other adverse eventsKAD-1229/KAD-1229 (Data Through Week 16)28118
Total, other adverse eventsKAD-1229 (Data Through Week 52)98175
Total, serious adverse eventsPlacebo/KAD-1229 (Data Through Week 16)260
Total, serious adverse eventsKAD-1229/KAD-1229 (Data Through Week 16)4118
Total, serious adverse eventsKAD-1229 (Data Through Week 52)18175

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/NCT02154347

GET https://conductscience.org/api/trials/v1/NCT02154347/events?page=2