Overview
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Indication
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Associated Conditions
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Research Report
Comprehensive Analysis of Agents and Trials Associated with the Identifier AD-223
I. Executive Summary
The identifier "AD-223" does not correspond to a singular pharmaceutical agent within the available information. Instead, it appears to be associated with at least three distinct entities, each with different characteristics, developmental stages, and therapeutic indications. This report synthesizes the available data to provide a clear delineation of these entities.
Firstly, "AD-223" refers to an investigational biologic therapeutic designed for the treatment of rheumatoid arthritis (RA). This agent functions by targeting and inhibiting Interleukin-17A (IL-17A), a key cytokine implicated in the inflammatory processes of RA. Early preclinical and clinical data suggest a promising efficacy and safety profile, leading to its progression into more extensive clinical trials.[1]
Secondly, the identifier "AD-223P3" designates a Phase 3 clinical trial. The context of the provided information suggests a potential association with Adlai Nortye. This trial reportedly investigates an agent, referred to as "AD-223" within the trial description, for the treatment of orthostatic hypotension. However, information regarding this trial is sparse and contains contradictory elements concerning its operational status.[2]
Thirdly, the numerical component "223" also appears in Radium Ra 223 dichloride (marketed as Xofigo), an approved radiopharmaceutical agent used for the treatment of castration-resistant prostate cancer with bone metastases.[3] It is crucial to distinguish this established therapeutic from the investigational entities also associated with "AD-223" to prevent misattribution of clinical data.
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
---|---|---|---|---|---|
2023/09/25 | Phase 3 | 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. |
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