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
Sponsor: Boehringer Ingelheim • ClinicalTrials.gov ID: NCT07768813
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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.
Interventions
-
Survodutide formulation A
(Combination product)
Pre-filled pen
-
Survodutide formulation B2
(Drug)
Survodutide formulation B2
Eligibility criteria
Conditions
Locations
- hVIVO Mannheim — Mannheim, Germany
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Data sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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