The objective of the trial is to assess the effect of single subcutaneous doses of dasiglucagon versus placebo on post-prandial plasma glucose nadir following a Mixed Meal Test in Roux-en-Y Gastric Bypass (RYGB) subjects
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
dasiglucagon SC, low dose
dasiglucagon SC, high dose
placebo for dasiglucagon
Nadir plasma glucose concentration
Time frame: From trial drug administration to 240 minutes after initiation of Mixed Meal Test
Percent time spent in hypoglycemia
Defined as time with a plasma glucose value of 70 mg/dL (3.9 mmol/L) or less
Time frame: From trial drug administration to 240 minutes after initiation of Mixed Meal Test
Percent time spent in clinical significant hypoglycemia
Defined as time with a plasma glucose value of 54 mg/dL (3.0 mmol/L) or less
Time frame: From trial drug administration to 240 minutes after initiation of Mixed Meal Test
Percent time spent in target range
Defined as time with a plasma glucose value of 70-180 mg/dL (3.9-10.0 mmol/L)
Time frame: From trial drug administration to 240 minutes after initiation of Mixed Meal Test
Percent time spent in hyperglycemia
Defined as time with a plasma glucose value \>180 mg/dL (\>10 mmol/l)
Time frame: From trial drug administration to 240 minutes after initiation of Mixed Meal Test
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