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A Trial Comparing Pharmacokinetics, Safety and Tolerability of Two Subcutaneous Concentrations of Dapiglutide

NCT06758583 PHASE1 COMPLETED

This is a phase 1, open-label, single-center, randomized, parallel-group trial designed to investigate the pharmacokinetic profiles, safety, and tolerability of a single dose administration of 7.5 mg dapiglutide administered s.c. with two drug product concentrations, 10 mg/mL and 25 mg/mL. The trial will be conducted in participants with a BMI ≥ 27.0 kg/m2.

Details

Lead sponsorZealand Pharma
PhasePHASE1
StatusCOMPLETED
Enrolment30
Start dateMon Dec 23 2024 00:00:00 GMT+0000 (Coordinated Universal Time)
CompletionFri Apr 25 2025 00:00:00 GMT+0000 (Coordinated Universal Time)

Conditions

Interventions

Countries

Germany