LivingGLP1
Study S003398

A First Human Dose Study Investigating Safety, Tolerability, and Pharmacokinetics of Oral Single Doses of NNC0113-6856 in Healthy Male Participants

Registration

Registration
NCT05521256
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
QUADRUPLE
Status
COMPLETED
Enrollment
70
Start
2022-08-26
Primary completion
2023-03-27
Lead sponsor
Novo Nordisk A/S
Conditions
Healthy Volunteers; Type 2 Diabetes
Interventions
DRUG:NNC0113-6856; DRUG:Placebo
Results posted
FALSE
Individual participant data sharing
YES
Secondary identifiers
OTHER:U1111-1270-0813; EUDRACT_NUMBER:2021-005397-26

Registered primary outcomes

  • Number of adverse events [From time of dosing (day 1) until completion of the follow-up visit (Day 42)]

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