Overview
No overview information available.
Indication
No indication information available.
Associated Conditions
No associated conditions information available.
Research Report
IBI3002: A Novel Bispecific Antibody Targeting IL-4Rα and TSLP for Inflammatory Diseases
1. Introduction to IBI3002
1.1. Overview: IBI3002 as a Novel Bispecific Antibody
IBI3002 is an investigational humanized bispecific antibody, distinguished as a potential first-in-class therapeutic agent engineered to concurrently target two critical mediators of inflammatory responses: Interleukin-4 receptor alpha (IL-4Rα) and thymic stromal lymphopoietin (TSLP).[1] The fundamental therapeutic strategy underpinning IBI3002 is the simultaneous blockade of these distinct, yet interconnected, pathways. These pathways are known to play pivotal roles in the pathophysiology of Type 2 (T2) and non-Type 2 (non-T2) inflammatory conditions, with a primary focus on asthma, and potential applications in other allergic and autoimmune diseases.[1]
The development of a bispecific antibody targeting both IL-4Rα and TSLP signifies a sophisticated advancement in the approach to managing complex inflammatory diseases. While therapies targeting individual components of these pathways have demonstrated clinical benefit, the heterogeneous nature of conditions like asthma, which involve multiple intersecting inflammatory cascades, often results in incomplete responses or the development of resistance to single-target agents. IL-4Rα blockade, exemplified by agents like dupilumab, addresses key Type 2 cytokines (IL-4 and IL-13), which are central to allergic inflammation. Concurrently, TSLP blockade, as seen with tezepelumab, targets an upstream epithelial-derived alarmin cytokine implicated in broader inflammatory cascades that encompass both T2 and non-T2 mechanisms. By engaging both targets, IBI3002 has the potential to offer synergistic effects, applicability to a wider patient demographic (including those with low eosinophil counts or mixed inflammatory profiles), and may overcome limitations observed with therapies directed at a single pathway, thereby aiming fo
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
---|---|---|---|---|---|
2025/06/11 | Phase 1 | Not yet recruiting | The First Affiliated Hospital of Soochow University | ||
2025/06/11 | Phase 1 | Recruiting | The First Affiliated Hospital of Soochow University | ||
2025/04/27 | Phase 1 | Recruiting | |||
2024/01/19 | Phase 1 | 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. |
Help Us Improve
Your feedback helps us provide better drug information and insights.