Patient-Reported Outcomes in People with Type 2 Diabetes Receiving Tirzepatide in the SURPASS Clinical Trial Programme

Author:

Boye Kristina S.,Thieu Vivian Thuyanh,Sapin Hélène,Lee Clare J.ORCID,Landó Laura Fernández,Brown Katelyn,Bray Ross,Wiese Russell J.ORCID,Patel HirenORCID,Rodríguez ÁngelORCID,Yu MariaORCID

Funder

Eli Lilly and Company

Publisher

Springer Science and Business Media LLC

Subject

Endocrinology, Diabetes and Metabolism,Internal Medicine

Reference37 articles.

1. United States Food and Drug Administration. Prescribing information: MOUNJARO (tirzepatide) injection, for subcutaneous use. Rockville, MD: FDA; 2022. p. 1–28. https://www.accessdata.fda.gov/drugsatfda_docs/label/2022/215866s000lbl.pdf. Accessed 5 Sept 2022.

2. European Commission. Mounjaro tirzepatide. Summary of product characteristics. Brussels: EC; 2022. p. 1–87. https://ec.europa.eu/health/documents/community-register/2022/20220915156773/anx_156773_en.pdf. Accessed 6 Oct 2022.

3. Pharmaceuticals and Medical Devices Agency (PMDA). Manjaro tirzepatide. General list entry. https://www.pmda.go.jp/PmdaSearch/iyakuDetail/GeneralList/24994A8. Accessed 20 Oct 2022.

4. Rosenstock J, Wysham C, Frías JP, et al. Efficacy and safety of a novel dual GIP and GLP-1 receptor agonist tirzepatide in patients with type 2 diabetes (SURPASS-1): a double-blind, randomised, phase 3 trial. Lancet. 2021;398:143–55.

5. Frías JP, Davies MJ, Rosenstock J, et al. Tirzepatide versus semaglutide once weekly in patients with type 2 diabetes. N Engl J Med. 2021;385:503–15.

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