LivingGLP1
Study S002022

A Trial to Demonstrate Bioequivalence Between Two Insulin Degludec/Liraglutide Formulations, B5 and V2 in Healthy Subjects

Registration

Registration
NCT01916174
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
DOUBLE
Status
COMPLETED
Enrollment
50
Start
2013-08
Primary completion
2013-11
Lead sponsor
Novo Nordisk A/S
Conditions
Diabetes; Diabetes Mellitus, Type 2; Healthy
Interventions
DRUG:insulin degludec/liraglutide
Results posted
FALSE
Secondary identifiers
EUDRACT_NUMBER:2012-005468-93; OTHER:U1111-1137-3809

Registered primary outcomes

  • Area under the serum IDeg concentration time curve after single dose [Assessed from 0 to 120 hours]
  • Maximum observed serum IDeg concentration after single dose [Assessed from 0-120 hours]
  • Area under the plasma liraglutide concentration time curve after single dose [Assessed from 0-72 hours]
  • Maximum observed plasma liraglutide concentration after single dose [Assessed from 0-72 hours]

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