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Trial · NCT04707326

Defining the Potency of DTG/3TC for Suppressed HIV Patients in Real-life: the DUALING Study

NCT04707326, Active not recruiting, Erasmus Medical Center; results first posted 2024-12-20

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Defining the Potency of DTG/3TC for Suppressed HIV Patients in Real-life: the DUALING Study. Trials, record NCT04707326. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT04707326

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Trial

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

Title
Defining the Potency of DTG/3TC for Suppressed HIV Patients in Real-life: the DUALING Study
NCT number
NCT04707326
Status
Active not recruiting
Enrollment
2,040 participants, actual
Lead sponsor
Erasmus Medical Center
Conditions
Hiv
Interventions
Dolutegravir / Lamivudine Pill
First posted
2021-01-13
Last updated
2024-12-20
Results first posted
2024-12-20
Limitations and caveats
All-Cause Mortality, Serious, or Other (non-serious) Adverse Events were collected during this study.

Source ClinicalTrials.gov

Registered outcomes2

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

ListOutcomeTime frameDescription
PrimaryEfficacy On Treatment (OT)1 yearProportion of subjects with treatment failure in the DTG/3TC versus 3-drug DTG containing cART group up to 1 year of follow up in the on treatment population
PrimaryEfficacy Intention to Treat (ITT)1 yearProportion of subjects with treatment failure in the DTG/3TC versus 3-drug DTG containing cART group up to 1 year of follow up in the intention to treat population.

Outcomes2

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYEfficacy On Treatment (OT)1 yearParticipantsCOUNT_OF_PARTICIPANTS
PRIMARYEfficacy Intention to Treat (ITT)1 yearParticipantsCOUNT_OF_PARTICIPANTS

Results by group8

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

OutcomeGroupCategoryValueSpreadUnits
Efficacy On Treatment (OT)DTG Based Switchers to DTG/3TC5Participants
Efficacy On Treatment (OT)DTG Based Triple Drug cART5Participants
Efficacy On Treatment (OT)Non-DTG Based Switchers to DTG/3TC2Participants
Efficacy On Treatment (OT)Non-DTG Based Triple Drug cART4Participants
Efficacy Intention to Treat (ITT)DTG Based Switchers to DTG/3TC34Participants
Efficacy Intention to Treat (ITT)DTG Based Triple Drug cART89Participants
Efficacy Intention to Treat (ITT)Non-DTG Based Switchers to DTG/3TC32Participants
Efficacy Intention to Treat (ITT)Non-DTG Based Triple Drug cART73Participants

Participant flow12

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDDTG Based Switchers to DTG/3TC390
Overall StudySTARTEDDTG Based Triple Drug cART780
Overall StudySTARTEDNon-DTG Based Switchers to DTG/3TC290
Overall StudySTARTEDNon-DTG Based Triple Drug cART580
Overall StudyCOMPLETEDDTG Based Switchers to DTG/3TC390
Overall StudyCOMPLETEDDTG Based Triple Drug cART780
Overall StudyCOMPLETEDNon-DTG Based Switchers to DTG/3TC290
Overall StudyCOMPLETEDNon-DTG Based Triple Drug cART580
Overall StudyNOT COMPLETEDDTG Based Switchers to DTG/3TC0
Overall StudyNOT COMPLETEDDTG Based Triple Drug cART0

Adverse events0

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

None in this release.

Adverse event totals12

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityDTG Based Switchers to DTG/3TC0390
Total, all-cause mortalityDTG Based Triple Drug cART0780
Total, all-cause mortalityNon-DTG Based Switchers to DTG/3TC0290
Total, all-cause mortalityNon-DTG Based Triple Drug cART0580
Total, other adverse eventsDTG Based Switchers to DTG/3TC0390
Total, other adverse eventsDTG Based Triple Drug cART0780
Total, other adverse eventsNon-DTG Based Switchers to DTG/3TC0290
Total, other adverse eventsNon-DTG Based Triple Drug cART0580
Total, serious adverse eventsDTG Based Switchers to DTG/3TC0390
Total, serious adverse eventsDTG Based Triple Drug cART0780

Papers1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed as
38567196DERIVED

Source PubMed

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/NCT04707326

GET https://conductscience.org/api/trials/v1/NCT04707326/registered