drugset / Trial / NCT07702890

A Three-part First-in-human Trial to Assess Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of GUB-UCN2 in Healthy Lean and Obese Participants and Participants With T2D

NCT07702890 ↗

Phase 1/2 Not yet recruiting 188 enrolled Gubra A/S
RandomizedSequentialDouble-blindTreatment

Summary

The trial will enroll healthy volunteers and individuals living with obesity, with and without Type 2 Diabetes. The study, with a treatment period of up to 16 weeks in selected cohorts, will investigate GUB-UCN2 as both a standalone therapy and on top of standard of care for obesity

Timeline

Start
2026-07
Primary completion
2028-12
Completion
2028-12

Drugs

EvaluationDrugModalityDoseRoute
Subject GUB-UCN2 Unknown — Subcutaneous