drugset / Trial / NCT07768813

A Study to Compare How 2 Different Formulations of Survodutide Are Taken up in the Body When Given by Injection in Healthy Men and Women With and Without Overweight or Obesity

NCT07768813 ↗

Phase 1 Recruiting 44 enrolled Boehringer Ingelheim
RandomizedCrossoverOpen-labelTreatment

Summary

The main objective of this trial is to establish the bioequivalence of survodutide in a pre-filled syringe (reference product \[formulation A\]) and in a vial (test product \[formulation B2\]) in male and female trial participants who are healthy or otherwise healthy with overweight/obesity, following subcutaneous administration.

Timeline

Start
2026-09-02
Primary completion
2026-12-08
Completion
2026-12-22

Drugs

EvaluationDrugModalityDoseRoute
Subject Survodutide Protein / enzyme biologic — Subcutaneous

Indications