LivingGLP1
crossover randomized trial

S003172

Design

Randomized
86
Start year
Treatment
0.4 weeks
Countries
Sponsor
(industry)
Eligibility
healthy adults 18 to 65 years; BMI 25 to 35 kg/m2; fasting glucose below 110 mg/dL

Conduct and analysis

Blinding
double blind
Sequence generation
not reported
Allocation concealment
not reported
Outcome adjudication
not reported
Primary estimand
not stated
Analysis population
completers
Missing data
completers only

Arms

ArmTreatmentBackgroundRandomizedAnalyzedCompleted treatment
A1exenatide
Exenatide IV infusion
lifestyle: not reported8674
A2Placebo
Placebo IV infusion
lifestyle: not reported8674
A3Moxifloxacin
Moxifloxacin 400 mg oral
lifestyle: not reported8674

Baseline characteristics

As printed in the trial reports or registry, per arm or for the whole trial.
CharacteristicStatisticExenatide IV infusion
A1
Placebo
A2
Moxifloxacin
A3
Whole trial
ALL
agemean (years)42
agesd (years)12
bmimean (kg/m2)28.4
bmisd (kg/m2)2.3
other malepercent91
whitepercent73

Results

6 adjudicated result lines, grouped by outcome. Open an outcome to see its values.
Serious adverse events (3 lines; O25)
WeekArmStatisticEstimateSE or SD95% CIEvents / NDetail
A1events0 / 86not stated; safety; R0026444:Results
A2events0 / 86not stated; safety; R0026444:Results
A3events0 / 86not stated; safety; R0026444:Results
Death by suicide (3 lines; O35B)
WeekArmStatisticEstimateSE or SD95% CIEvents / NDetail
A1events0 / 86not stated; safety; R0026444:Results
A2events0 / 86not stated; safety; R0026444:Results
A3events0 / 86not stated; safety; R0026444:Results