LivingGLP1
Study S000019

A Randomised, Double-blind Within Dose Group, Single-centre, Placebo-controlled, Parallel 2-different Dose Group, 14-day Multiple s.c. Doses Study to Assess the Safety, Pharmacokinetics and Pharmacodynamics of Liraglutide (NNC 90-1170) in Subjects With Type 2 Diabetes

Registration

Registration
NCT01615978
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
DOUBLE
Status
COMPLETED
Enrollment
15
Start
2003-12
Primary completion
2004-03
Lead sponsor
Novo Nordisk A/S
Conditions
Diabetes; Diabetes Mellitus, Type 2
Interventions
DRUG:liraglutide; DRUG:placebo
Results posted
FALSE

Registered primary outcomes

  • 24-hour profiles of serum calcitonin []
  • 24-hour profiles of Ca2+ (ionised calcium) []
  • 24-hour profiles of PTH (Parathyroid Hormone) []
  • Adverse events []

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