TrialSignal
Clinical trial intelligence report
A Pilot Study to Determine Tolerability to Glucagon Infusion in Obese Subjects
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jun 17, 2026
NCT ID
NCT02817659
Status
ACTIVE_NOT_RECRUITING
Phase
Phase 1
Sponsor
AdventHealth Translational Research Institute
Executive brief
Investment-Ready Snapshot
The pilot study sponsored by AdventHealth Translational Research Institute aims to assess the tolerability of glucagon infusion in obese subjects, which could have significant implications for obesity management and metabolic disorders. Given the increasing prevalence of obesity globally, successful outcomes may position glucagon as a viable therapeutic option, potentially competing with existing weight management drugs such as GLP-1 agonists. The study's focus on tolerability is critical, as adverse effects can limit patient adherence and market uptake. The asset's development could attract interest from larger pharmaceutical companies looking to expand their obesity treatment portfolios, particularly if the results indicate a favorable safety profile. However, the competitive landscape includes established therapies, necessitating a robust differentiation strategy.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT02817659
Indication
Obesity
Modality
small molecule
Target
Glucagon receptor (GCGR)
Intervention
Glucagon
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.