Overview
Elraglusib is under investigation in clinical trial NCT04218071 (Actuate 1901: 9-ING-41 in Myelofibrosis).
Indication
No indication information available.
Associated Conditions
No associated conditions information available.
Research Report
Elraglusib (9-ING-41): A Comprehensive Profile of a Clinically Promising Agent with a Contested Mechanism
Section 1: Executive Summary
Elraglusib (9-ING-41) is an investigational, first-in-class, small-molecule therapeutic developed by Actuate Therapeutics, Inc..[1] Originally conceived and advanced into clinical trials as a potent inhibitor of Glycogen Synthase Kinase-3 Beta (GSK-3β), a key enzyme implicated in numerous oncogenic signaling pathways, Elraglusib has demonstrated a compelling clinical profile, particularly in cancers with high unmet medical needs.[2] The most significant clinical achievement to date is from the randomized, controlled Phase 2 Actuate-1801 trial, where the addition of Elraglusib to standard-of-care chemotherapy resulted in a statistically significant and clinically meaningful improvement in overall survival for patients with previously untreated metastatic pancreatic ductal adenocarcinoma (mPDAC).[3] This pivotal result has positioned Elraglusib as a potential paradigm-shifting treatment in one of oncology's most challenging indications.
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
|---|---|---|---|---|---|
2025/03/26 | Phase 1 | Recruiting | Anwaar Saeed | ||
2022/02/14 | Phase 2 | Terminated | Anwaar Saeed | ||
2021/11/11 | Phase 2 | Withdrawn | |||
2021/10/14 | Phase 2 | Active, not recruiting | Colin D. Weekes, M.D., PhD | ||
2021/08/18 | Phase 2 | Active, not recruiting | Glenn J. Hanna | ||
2021/05/28 | Phase 2 | Withdrawn | |||
2021/04/05 | Phase 2 | Withdrawn | |||
2020/01/23 | Phase 1 | Terminated | |||
2020/01/06 | Phase 2 | Completed | |||
2018/09/20 | Phase 2 | Active, not recruiting |
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. | |||||
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