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Clinical trial intelligence report
A Double-blind, Placebo-controlled, Randomized Study to Evaluate the Efficacy and Safety of KBP-042 in Patients With Type 2 Diabetes
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jun 24, 2026
Report code
NCT03230786-Jun 24, 2026
NCT ID
NCT03230786
Status
COMPLETED
Phase
Phase 2
Sponsor
KeyBioscience AG
Executive brief
Investment-Ready Snapshot
KBP-042, developed by KeyBioscience AG, is positioned as a potential treatment for patients with Type 2 Diabetes Mellitus who have inadequate glycaemic control on metformin. The trial's multicentre approach across several European countries (Czech Republic, Denmark, Moldova, Poland, Romania, and the United Kingdom) indicates a strategic effort to capture a diverse patient population. The competitive landscape includes existing therapies such as GLP-1 receptor agonists and SGLT2 inhibitors, which dominate the market. Successful outcomes could enhance KeyBioscience's portfolio and provide a new treatment option in a crowded market, potentially leading to partnerships or acquisition interest from larger pharmaceutical companies. Diligence should focus on the trial's efficacy and safety results, as well as the regulatory pathway for DACRAs.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT03230786
Indication
Type 2 Diabetes Mellitus
Modality
small molecule
Target
Dual amylin and calcitonin receptor agonists (DACRAs)
Intervention
Daily injection of KBP/placebo for 12 weeks as add-on to metformin
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.