LivingGLP1
parallel randomized trial

S003426

Design

Randomized
79
Start year
Treatment
24 weeks, follow-up 24 weeks
Countries
Pakistan (1 sites)
Sponsor
(non industry)
Eligibility
adults with type 2 diabetes; HbA1c 6.5 to 8.0 percent; BMI 30 to 35; stable metformin and empagliflozin

Conduct and analysis

Blinding
open label
Sequence generation
not reported
Allocation concealment
not reported
Outcome adjudication
not reported
Primary estimand
not stated
Analysis population
Missing data
not reported

Arms

ArmTreatmentBackgroundRandomizedAnalyzedCompleted treatment
A1Semaglutide 0.5 mg subcutaneous once weekly
Semaglutide 0.5 mg once weekly
metformin 2 g/day and empagliflozin 25 mg/day; lifestyle: standard3838
A2Tirzepatide 5 mg subcutaneous once weekly
Tirzepatide 5 mg once weekly
metformin 2 g/day and empagliflozin 25 mg/day; lifestyle: standard4141

Baseline characteristics

As printed in the trial reports or registry, per arm or for the whole trial.
CharacteristicStatisticSemaglutide 0.5 mg subcutaneous once weekly
A1
Tirzepatide 5 mg subcutaneous once weekly
A2
age
sex:female
mean (years)47.048.0
age
sex:male
mean (years)52.050.5
bmimean (kg/m2)33.834.2
femalen2227
femalepercent57.965.9
hba1cmean (percent)7.77.9

Analyses this trial contributes to

Results

11 adjudicated result lines, grouped by outcome. Open an outcome to see its values.
HbA1c change (3 lines; O01)
WeekArmStatisticEstimateSE or SD95% CIEvents / NDetail
24A1change-0.9 percent38not stated; other; R0040396:Table 2
24A1 vs A2md0.5 percentnot stated; other; R0040396:Table 2
24A2change-1.4 percent41not stated; other; R0040396:Table 2
Level 2 or 3 hypoglycemia (participants) (3 lines; O04)
WeekArmStatisticEstimateSE or SD95% CIEvents / NDetail
A1events1 / 38not stated; safety; R0040396:Table 3
A1 vs A2or0.53not stated; safety; R0040396:Table 3
A2events2 / 41not stated; safety; R0040396:Table 3
Discontinuation due to adverse events (2 lines; O26)
WeekArmStatisticEstimateSE or SD95% CIEvents / NDetail
A1events3 / 38not stated; safety; R0040396:Abstract
A2events2 / 41not stated; safety; R0040396:Abstract
Discontinuation due to gastrointestinal adverse events (3 lines; O27E)
WeekArmStatisticEstimateSE or SD95% CIEvents / NDetail
A1events3 / 38not stated; safety; R0040396:Table 3
A1 vs A2or1.67not stated; safety; R0040396:Table 3
A2events2 / 41not stated; safety; R0040396:Table 3