LivingGLP1
Study S000481

A Trial to Demonstrate Bioequivalence Between Semaglutide Formulation D With the DV3396 Pen-injector and Formulation B With the PDS290 Pen-injector in Subjects With Overweight or Obesity

Registration

Registration
NCT04187300
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
NONE
Status
COMPLETED
Enrollment
68
Start
2019-12-16
Primary completion
2020-09-23
Lead sponsor
Novo Nordisk A/S
Conditions
Overweight; Obesity
Interventions
DRUG:Semaglutide
Results posted
FALSE
Individual participant data sharing
YES
Secondary identifiers
OTHER:U1111-1236-7697; REGISTRY:2019-002909-21; NIH:2019

Registered primary outcomes

  • AUC0-168h,2.4mg,SS, Area under the semaglutide concentration time curve [0-168 hours (Day 141-148) after last 2.4 mg dose]
  • Cmax,2.4mg,SS, Maximum observed semaglutide concentration [0-168 hours (Day 141-148) after last 2.4 mg dose]

Linked records (0)

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