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Research Report
PF-07275315: A Trispecific Antibody Poised to Redefine the Treatment of Type 2 Inflammation
Executive Summary
PF-07275315 is a first-in-class, investigational trispecific monoclonal antibody being developed by Pfizer as a potential cornerstone therapy for Type 2 inflammatory diseases.[1] Classified as a New Molecular Entity (NME), this biologic therapeutic is engineered with a novel mechanism of action (MoA) that simultaneously targets and inhibits three key cytokines central to the pathophysiology of atopic conditions: Interleukin-4 (
IL−4), Interleukin-13 (IL−13), and Thymic Stromal Lymphopoietin (TSLP).[2] This multi-pronged approach represents a significant evolution from existing biologics, which typically target one or two of these pathways. The strategic rationale is to achieve a more comprehensive and synergistic blockade of the Type 2 inflammatory cascade, targeting both the upstream initiation signal (TSLP) and the key downstream effector cytokines (
IL−4/IL−13) that perpetuate the disease process.[4]
Currently, PF-07275315 is advancing through Phase II of clinical development for two major indications: moderate-to-severe atopic dermatitis (AD) and moderate-to-severe asthma.[1] The clinical program is designed to rigorously evaluate its efficacy and safety in patient populations with significant unmet medical needs, including those who have had an inadequate response to current standards of care.[7]
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
---|---|---|---|---|---|
2025/05/18 | Phase 2 | Recruiting | |||
2024/11/05 | Phase 1 | Completed | |||
2023/08/16 | Phase 2 | Recruiting | |||
2022/06/09 | 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
Approved Product | Company | Approval Number | Drug Type | Dosage Form | Approval Date |
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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
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
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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 |
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No UK EMC drug information found for this drug. |
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