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Research Report
AZD9550: An Investigational Dual GLP-1R/GCGR Agonist for Metabolic Diseases
1. Executive Summary
AZD9550 is an investigational therapeutic agent under development by AstraZeneca, characterized by its dual agonism at the glucagon-like peptide-1 receptor (GLP-1R) and the glucagon receptor (GCGR).[1] This compound is strategically positioned within AstraZeneca's Cardiovascular, Renal and Metabolism (CVRM) pipeline and is being evaluated for the treatment of complex metabolic disorders, primarily obesity and non-alcoholic steatohepatitis (NASH), now increasingly referred to as metabolic dysfunction-associated steatohepatitis (MASH).[1] Potential utility in Type 2 Diabetes Mellitus (T2DM) is also implicitly under investigation, given the study populations.[1] AZD9550 is administered via subcutaneous (SC) or intravenous (IV) routes, with the SC route being the focus for therapeutic delivery in later-phase trials.[2] Currently, the drug is advancing through Phase I/II and Phase IIb clinical trials.[1] A key aspect of its development strategy involves evaluating its efficacy and safety both as a monotherapy and in combination with AZD6234, a long-acting amylin analogue also developed by AstraZeneca, particularly for obesity management.[9] The simultaneous targeting of obesity and NASH/MASH underscores a therapeutic approach aimed at addressing the interconnected pathophysiology common to these prevalent metabolic conditions, leveraging the compound's dual mechanism of action to potentially achieve broader metabolic benefits than single-pathway agents.
2. Introduction to AZD9550
2.1. Identification and Development
The investigational drug AZD9550, also referred to as AZD 9550, is a novel compound originated and developed by the global biopharmaceutical company AstraZeneca.[1] It represents a focused effort within AstraZeneca's extensive research and development pipeline, specifically targeting metabolic diseases.[4]
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
|---|---|---|---|---|---|
2025/06/12 | Phase 2 | Recruiting | |||
2025/06/10 | Phase 1 | Recruiting | |||
2025/03/06 | Phase 2 | Active, not recruiting | |||
2023/11/30 | Phase 1 | Recruiting | |||
2023/05/08 | Phase 1 | Completed |
FDA Drug Approvals
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| No FDA approvals found for this drug. | |||||
EMA Drug Approvals
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| No EMA approvals found for this drug. | |||
HSA Drug Approvals
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| No HSA approvals found for this drug. | |||||
NMPA Drug Approvals
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| No NMPA approvals found for this drug. | |||||
PPB Drug Approvals
Approved Product | Registration No. | Company | Licence No. | Strength | Registration Date |
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| No PPB approvals found for this drug. | |||||
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
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| No TGA approvals found for this drug. | |||||
Health Canada Drug Approvals
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| No Health Canada approvals found for this drug. | |||||
CIMA AEMPS Drug Approvals
Approved Product | Company | Registration Number | Pharmaceutical Form | Prescription Type | Status |
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| No CIMA AEMPS (Spain) approvals found for this drug. | |||||
Philippines FDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
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| No Philippines FDA approvals found for this drug. | |||||
Saudi SFDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
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| No Saudi SFDA approvals found for this drug. | |||||
Malaysia NPRA Drug Approvals
Approved Product | Company | Registration Number | Dosage Form | Strength | Approval Date |
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| 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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