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
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Survodutide | Protein / enzyme biologic | — | Subcutaneous |