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Clinical trial intelligence report
A Regulatory Requirement Non Interventional Study to Monitor the Safety and Effectiveness of Trajenta (Linagliptin, 5 mg, q.d) in Korean Patients With Type 2 Diabetes Mellitus(SELINA Study)
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT01707147-Jul 28, 2026
NCT ID
NCT01707147
Status
COMPLETED
Phase
Completed (Post-Marketing Surveillance)
Sponsor
Boehringer Ingelheim
Executive brief
Investment-Ready Snapshot
The SELINA study, sponsored by Boehringer Ingelheim, evaluated the safety and effectiveness of Trajenta (linagliptin) in a real-world setting among Korean patients with Type 2 Diabetes Mellitus. With a significant enrollment of 3,219 patients, the study provides valuable post-marketing data that can enhance the product's positioning in the competitive diabetes market in South Korea. Given the increasing prevalence of diabetes in Asia, the findings may support ongoing marketing efforts and inform future product development strategies. The collaboration with Eli Lilly indicates a strategic partnership that may enhance market access and distribution capabilities.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT01707147
Indication
Diabetes Mellitus, Type 2
Modality
small molecule
Target
Dipeptidyl peptidase-4 (DPP-4) enzyme inhibition
Intervention
Trajenta tablet
Source record
Protocol Description
Detailed source ingestion pending.
Source record
Outcome Measures
Detailed source ingestion pending.
Source record
Eligibility
Detailed source ingestion pending.
AI analysis
Known Results And Readout Context
Detailed source ingestion pending.
IP intelligence
Patent And IP Landscape
Detailed source ingestion pending.
Source record
Contacts
Detailed source ingestion pending.