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Phase 1a: First-in-Human Single Ascending Dose Study (NCT02951806) Study Title: "Safety, Tolerability, and Pharmacokinetics of Single Doses of Cagrilintide in Healthy Subjects" Status: Completed Phase: Phase 1a Enrollment: 48 healthy volunteers Study Period: 2016-2017 Location: Single center (Denmark) Design: Randomized, double-blind, placebo-controlled, single ascending dose Dose Range: 0.03-10 mg SC Primary Endpoints: Safety, tolerability, PK parameters Population: Healthy male subjects, BMI 20-28 Key Results: Pharmacokinetics: Terminal half-life 5-7 days across dose range

Vial Strength This indicates the total amount of peptide in the vial

One study reports about a 50% drop in eNOScaveolin-1 binding

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All clinical trial data, research findings, and scientific information presented on this page are sourced from peer-reviewed academic publications

10.1007/BF02051930 [DOI] [PubMed] [Google Scholar] Hinterseher I., Schworer C