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Glucagon 12.5ng/kg/min
Glucagon binds to glucagon receptors on hepatic and other cells to stimulate glycogenolysis and gluconeogenesis, rapidly raising blood glucose levels.
Glucagon binds to glucagon receptors on hepatic and other cells to stimulate glycogenolysis and gluconeogenesis, rapidly raising blood glucose levels. Used for Acute hypoglycemia (severe or refractory), Hypoglycemia in critical care settings.
At a glance
| Generic name | Glucagon 12.5ng/kg/min |
|---|---|
| Sponsor | Cambridge University Hospitals NHS Foundation Trust |
| Drug class | Glucagon receptor agonist |
| Target | Glucagon receptor (GCGR) |
| Modality | Small molecule |
| Therapeutic area | Endocrinology |
| Phase | FDA-approved |
Mechanism of action
Glucagon is a peptide hormone that activates G-protein coupled glucagon receptors, primarily on hepatocytes, triggering intracellular signaling cascades that mobilize stored glycogen and promote glucose synthesis. This results in rapid elevation of blood glucose, making it effective for acute hypoglycemia reversal. The dose specified (12.5 ng/kg/min) suggests continuous intravenous infusion, likely for severe or refractory hypoglycemia management in a clinical setting.
Approved indications
- Acute hypoglycemia (severe or refractory)
- Hypoglycemia in critical care settings
Common side effects
- Hyperglycemia
- Nausea
- Vomiting
- Tachycardia
- Hypokalemia
Key clinical trials
Primary sources
Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.
| Source | Used for |
|---|---|
| ClinicalTrials.gov | Trial enrolment, design, endpoints, results |
Competitive intelligence
For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape:
- Glucagon 12.5ng/kg/min CI brief — competitive landscape report
- Glucagon 12.5ng/kg/min updates RSS · CI watch RSS
- Cambridge University Hospitals NHS Foundation Trust portfolio CI