This promotional website has been developed, organised and funded by Boehringer Ingelheim.
Prescribing information for the United Kingdom and Republic of Ireland.
Adverse event reporting information can be found at the bottom of the page.
Proven efficacy vs placebo1,9
Proven efficacy vs placebo:1,9 The efficacy and safety of 5 mg linagliptin was evaluated in eight phase III randomised controlled trials. Linagliptin once daily demonstrated clinically significant improvements in glycaemic control vs placebo or comparator.1
Demonstrated CV and kidney safety profile
Long-term cardiovascular and kidney safety profile of TRAJENTA® has been demonstrated in two cardiovascular outcome trials.10–16 As TRAJENTA® is primarily excreted via the bile, it is suitable for a broad range of adults with type 2 diabetes independent of renal function.1
Unique convenience of one dose, once daily1
The recommended dose of TRAJENTA® for adult patients with type 2 diabetes is 5 mg once daily, independent of renal and hepatic function, body mass index, age, ethnicity, background type 2 diabetes therapy, and disease duration.1,16
Watch the most recent webinar
§ Treatment difference of 0.8% in favour of linagliptin for adjusted mean HbA1c reduction at 24 weeks between linagliptin and placebo groups.
CKD: chronic kidney disease; CV: cardiovascular; SmPC: Summary of Product Characteristics.
*Summary of Product Characteristics for Trajenta, sitagliptin, vildagliptin and saxagliptin are available at: https://www.medicines.org.uk (UK) and https://www.medicines.ie/ (ROI).
**Summary of Product Characteristics for alogliptin is available at: https://www.medicines.org.uk (UK).
Trajenta is indicated in adults with type 2 diabetes mellitus as an adjunct to diet and exercise to improve glycaemic control as:
• monotherapy when metformin is inappropriate due to intolerance, or contraindicated due to renal impairment
• in combination with other medicinal products for the treatment of diabetes, including insulin, when these do not provide adequate glycaemic control
The content has been reviewed and approved by the sponsoring company prior to its publication. Editorial support for this website has been provided by
OmniaMed Communications.
PC-GB-106627 V10 | March 2025
Copyright 2025 Oxbridge Solutions Limited®, a subsidiary of OmniaMed Communications Limited. All rights reserved. Any distribution or duplication of the information contained herein is strictly prohibited. Oxbridge Solutions receives funding from advertising but maintains editorial independence.