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International, Randomized, Open Label Study to Compare the Safety and Efficacy of Lixisenatide vs. Sulfonylurea on Top of Basal Insulin Treatment in Type 2 Diabetes Mellitus Subjects Who Elect to Fast During Ramadan
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jun 24, 2026
Report code
NCT02941367-Jun 24, 2026
NCT ID
NCT02941367
Status
COMPLETED
Phase
Phase 3b
Sponsor
Sanofi
Executive brief
Investment-Ready Snapshot
The LixiRam study, sponsored by Sanofi, evaluates the safety and efficacy of Lixisenatide compared to Sulfonylurea in patients with Type 2 Diabetes Mellitus who intend to fast during Ramadan. This trial is particularly relevant given the growing prevalence of diabetes in the Middle East and South Asia, where fasting during Ramadan is common. The results could position Lixisenatide favorably against traditional therapies, potentially increasing its market share in the diabetes treatment landscape. The trial's completion and subsequent data could enhance Sanofi's competitive edge, especially in regions with significant Muslim populations. Additionally, the focus on safety during fasting may attract attention from healthcare providers and patients alike, emphasizing the importance of tailored diabetes management strategies.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT02941367
Indication
Diabetes Mellitus, Type 2
Modality
small molecule
Target
GLP-1 receptor agonist
Intervention
Lixisenatide (AVE0010), Sulfonylurea, metformin, basal insulin
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.