LivingGLP1
Study S001925

A Study Investigating Pharmacokinetic Properties When Dosing Different Formulations of Oral Peptide Therapeutics in Healthy Male Participants

Registration

Registration
NCT05129891
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
NONE
Status
COMPLETED
Enrollment
384
Start
2021-11-03
Primary completion
2023-02-26
Lead sponsor
Novo Nordisk A/S
Conditions
Healthy Volunteers; High Blood Cholesterol Levels; Type 2 Diabetes
Interventions
DRUG:Semaglutide D; DRUG:Semaglutide G; DRUG:Semaglutide H; DRUG:Semaglutide I; DRUG:NNC0385-0434 B; DRUG:NNC0385-0434 C; DRUG:NNC0385-0434 D; DRUG:NNC0385-0434 E
Results posted
FALSE
Individual participant data sharing
YES
Secondary identifiers
OTHER:U1111-1266-0672; EUDRACT_NUMBER:2021-001452-34

Registered primary outcomes

  • AUC0-24h,API,day10; area under the API plasma concentration-time curve from 0 to 24 hours after the 10th dose [From pre-dose PK sample (0 hours) at day 10 to PK sample 24 hours after dose administration]

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