LivingGLP1
Study S000764

A Randomised, Double-blind, Single-centre, Three-period, Cross-over Trial in Healthy Subjects Investigating the Bioequivalence Between Each of the Two New Liraglutide Formulations at pH 7.9 and 8.15 and the Planned Phase 3 Formulation at pH 7.7

Registration

Registration
NCT01514487
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
DOUBLE
Status
COMPLETED
Enrollment
24
Start
2005-01-13
Primary completion
2005-03-30
Lead sponsor
Novo Nordisk A/S
Conditions
Diabetes; Healthy
Interventions
DRUG:liraglutide
Results posted
FALSE

Registered primary outcomes

  • Area under the Curve (0-t) []
  • Cmax, maximum concentration []

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