Overview
No overview information available.
Indication
No indication information available.
Associated Conditions
No associated conditions information available.
Research Report
Ervogastat (PF-06865571): A Novel DGAT2 Inhibitor for Metabolic Dysfunction-Associated Steatohepatitis
1. Introduction to Ervogastat (PF-06865571)
Overview and Significance in NASH/MASH Treatment Landscape
Ervogastat, also known by its development code PF-06865571, is an investigational small molecule therapeutic agent currently under development by Pfizer Inc..[1] This compound has garnered attention as a potentially significant advancement in the challenging field of Metabolic Dysfunction-Associated Steatohepatitis (MASH), a condition previously referred to as Non-alcoholic Steatohepatitis (NASH). The focus of ervogastat's development is particularly on patients who present with liver fibrosis, a critical factor in disease progression.[2]
The landscape of MASH treatment is characterized by a profound unmet medical need. It is a progressive liver disease that, until very recently, had no therapies approved by major regulatory bodies like the U.S. Food and Drug Administration (FDA) or the European Medicines Agency (EMA).[4] The potential consequences of untreated MASH are severe, including the development of cirrhosis, liver failure, and hepatocellular carcinoma, underscoring the urgency for effective pharmacological interventions.[4]
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
---|---|---|---|---|---|
2020/05/22 | Phase 2 | Completed | |||
2020/03/25 | Phase 2 | Completed | |||
2018/07/20 | Phase 1 | Completed | |||
2018/05/01 | Phase 1 | Completed | |||
2017/07/26 | Phase 1 | Completed | |||
2017/03/27 | Phase 1 | Completed |
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
---|---|---|---|---|---|
No FDA approvals found for this drug. |
EMA Drug Approvals
Approved Product | Authorization Holder | Status | Issued Date |
---|---|---|---|
No EMA approvals found for this drug. |
HSA Drug Approvals
Approved Product | Manufacturer | Approval Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
No HSA approvals found for this drug. |
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 |
---|---|---|---|---|---|
No TGA approvals found for this drug. |
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
---|---|---|---|---|---|
No Health Canada approvals found for this drug. |
CIMA AEMPS Drug Approvals
Approved Product | Company | Registration Number | Pharmaceutical Form | Prescription Type | Status |
---|---|---|---|---|---|
No CIMA AEMPS (Spain) approvals found for this drug. |
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. |
Help Us Improve
Your feedback helps us provide better drug information and insights.