A Phase 3 Trial to Evaluate the Safety and Efficacy of HDM1002 Tablets in Overweight and Obese Adults
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
780
HDM1002 200mg, oral, once daily, 52 weeks
HDM1002 400mg, oral, once daily, 52 weeks
HDM1002 placebo, oral, once daily, 52 weeks
Percentage Change From Baseline in Body Weight
Weight was recorded in kilograms (kg), and accuracy to the nearest 0.1 kg,
Time frame: 44weeks
Percentage Change of Participants Achieving Weight Loss ≥ 5%
Weight was recorded in kilograms (kg), and accuracy to the nearest 0.1 kg
Time frame: 44weeks
Percentage Change of Participants Achieving Weight Loss ≥ 10% and ≥ 15%
Weight was recorded in kilograms (kg), and accuracy to the nearest 0.1 kg.
Time frame: 44weeks
Change From Baseline in Waist Circumference
Waist Circumference was recorded in cm
Time frame: 44 weeks, 52 weeks
Percentage Change of Participants Achieving Weight Loss ≥ 5% , ≥ 10% and ≥ 15%
Weight was recorded in kilograms (kg), and accuracy to the nearest 0.1 kg.
Time frame: 52 weeks
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