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Clinical trial intelligence report
Post Marketing Surveillance in Japan on Long Term Drug Use of JARDIANCE® Tablets in Patients With Type 2 Diabetes Mellitus
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT02489942-Jul 28, 2026
NCT ID
NCT02489942
Status
COMPLETED
Phase
Post-Marketing Surveillance
Sponsor
Boehringer Ingelheim
Executive brief
Investment-Ready Snapshot
JARDIANCE (empagliflozin), developed by Boehringer Ingelheim in collaboration with Eli Lilly, is positioned as a leading treatment for Type 2 Diabetes Mellitus (T2DM) in Japan. The completion of this extensive post-marketing surveillance study with over 8,000 participants reinforces its safety and efficacy profile, which is critical for maintaining market share against competitors such as Farxiga (dapagliflozin) and Invokana (canagliflozin). The findings may enhance physician confidence in prescribing JARDIANCE, potentially leading to increased market penetration. Additionally, the study's results could support further regulatory submissions or label expansions, thereby enhancing commercial opportunities.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT02489942
Indication
Diabetes Mellitus, Type 2
Modality
small molecule
Target
Sodium-glucose cotransporter 2 (SGLT2)
Intervention
Jardiance
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.