Overview
Glucagon is a 29 amino acid hormone used as a diagnostic aid in radiologic exams to temporarily inhibit the movement of the gastrointestinal tract and to treat severe hypoglycemia. Glucagon raises blood sugar through activation of hepatic glucagon receptors, stimulating glycogenolysis and the release of glucose. Glucagon was granted FDA approval on 14 November 1960.
Indication
Glucagon is indicated as a diagnostic aid in radiologic exams to temporarily inhibit the movement of the gastrointestinal tract and to treat severe hypoglycemia.
Associated Conditions
- Severe Hypoglycemia
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
|---|---|---|---|---|---|
2025/05/23 | Phase 4 | Recruiting | |||
2025/03/12 | Not Applicable | Not yet recruiting | |||
2024/09/19 | Phase 1 | Recruiting | |||
2024/08/16 | Phase 1 | Not yet recruiting | |||
2024/02/09 | N/A | Recruiting | |||
2023/11/13 | Phase 1 | Withdrawn | |||
2023/07/25 | Phase 2 | Terminated | St. Olavs Hospital | ||
2023/02/13 | Phase 1 | Suspended | |||
2022/08/15 | Phase 1 | Recruiting | |||
2022/01/28 | N/A | Active, not recruiting |
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
|---|---|---|---|---|---|
| Xeris Pharmaceuticals, Inc. | 72065-141 | SUBCUTANEOUS | 1 mg in 0.2 mL | 9/26/2023 | |
| Xeris Pharmaceuticals, Inc. | 72065-140 | SUBCUTANEOUS | 1 mg in 0.2 mL | 9/26/2023 | |
| Xeris Pharmaceuticals, Inc. | 72065-130 | SUBCUTANEOUS | 0.5 mg in 0.1 mL | 9/26/2023 | |
| Eli Lilly and Company | 0002-6145 | NASAL | 3 mg in 1 1 | 8/16/2021 | |
| Xeris Pharmaceuticals, Inc. | 72065-121 | SUBCUTANEOUS | 1 mg in 0.2 mL | 9/26/2023 | |
| Healing Power Within Inc. | 51264-0001 | ORAL | 30 [hp_X] in 1 mL | 5/23/2025 | |
| Xeris Pharmaceuticals, Inc. | 72065-131 | SUBCUTANEOUS | 1 mg in 0.2 mL | 9/26/2023 | |
| Xeris Pharmaceuticals, Inc. | 72065-120 | SUBCUTANEOUS | 0.5 mg in 0.1 mL | 9/26/2023 | |
| Next Generation Health | 69192-0001 | ORAL | 30 [hp_X] in 1 mL | 5/22/2025 |
EMA Drug Approvals
Approved Product | Authorization Holder | Status | Issued Date |
|---|---|---|---|
Authorised | 2/11/2021 | ||
Authorised | 12/16/2019 |
HSA Drug Approvals
Approved Product | Manufacturer | Approval Number | Dosage Form | Strength | Approval Date |
|---|---|---|---|---|---|
| GLUCAGEN FOR INJECTION 1 mg/ml | SIN09070P | INJECTION, POWDER, FOR SOLUTION | 1mg/ml | 12/9/1996 |
NMPA Drug Approvals
Approved Product | Company | Approval Number | Drug Type | Dosage Form | Approval Date |
|---|---|---|---|---|---|
| No NMPA approvals found for this drug. | |||||
PPB Drug Approvals
Approved Product | Registration No. | Company | Licence No. | Strength | Registration Date |
|---|---|---|---|---|---|
| No PPB approvals found for this drug. | |||||
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
|---|---|---|---|---|---|
| GLUCAGEN HYPOKIT 1mg powder for injection vial with diluent syringe | 47105 | Medicine | A | 2/28/1994 |
CIMA AEMPS Drug Approvals
Approved Product | Company | Registration Number | Pharmaceutical Form | Prescription Type | Status |
|---|---|---|---|---|---|
| BAQSIMI 3 MG POLVO NASAL EN ENVASE UNIDOSIS | 1191406001 | POLVO NASAL | Medicamento Sujeto A Prescripción Médica | Commercialized |
Philippines FDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
|---|---|---|---|---|---|
| No Philippines FDA approvals found for this drug. | |||||
Saudi SFDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
|---|---|---|---|---|---|
| No Saudi SFDA approvals found for this drug. | |||||
Malaysia NPRA Drug Approvals
Approved Product | Company | Registration Number | Dosage Form | Strength | Approval Date |
|---|---|---|---|---|---|
| No Malaysia NPRA approvals found for this drug. | |||||
UK EMC Drug Information
Medicine Name | MA Holder | MA Number | Pharmaceutical Form | Active Ingredient | Authorization Date |
|---|---|---|---|---|---|
| No UK EMC drug information found for this drug. | |||||
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