LivingGLP1
Study S001103

A Trial to Demonstrate Bioequivalence Between Semaglutide Drug Product Concentrations 0.68 mg/mL and 1.0 mg/mL

Registration

Registration
NCT04228354
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
QUADRUPLE
Status
COMPLETED
Enrollment
28
Start
2020-01-29
Primary completion
2020-06-01
Lead sponsor
Novo Nordisk A/S
Conditions
Healthy Volunteers; Overweight; Obesity
Interventions
DRUG:Semaglutide
Results posted
FALSE
Individual participant data sharing
YES
Secondary identifiers
OTHER:U1111-1241-6257; REGISTRY:2019-004020-37; NIH:2019

Registered primary outcomes

  • Area under the semaglutide plasma concentration curve from 0 to tz [0-840 hours]
  • Maximum semaglutide plasma concentration [0-840 hours]

Linked records (0)

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