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Research Report
Incomplete Freund's Adjuvant (DB17475): An Immunological and Developmental Analysis
Executive Summary
Incomplete Freund's Adjuvant (IFA), identified by DrugBank accession number DB17475, is a potent, investigational immunological adjuvant with a long and complex history in biomedical research. Classified as a biotech product and complex mixture, IFA is a water-in-oil emulsion composed of non-metabolizable mineral oil (paraffin oil) and a surfactant (mannide monooleate).[1] Its primary mechanism of action involves the formation of a depot at the injection site, which facilitates the slow, sustained release of an emulsified antigen. This prolonged antigen exposure, coupled with the recruitment of innate immune cells, drives a powerful and predominantly T-helper 2 (Th2)-biased humoral immune response, characterized by the production of high-titer, long-lasting antibodies.[2]
For decades, IFA has served as a foundational tool in preclinical research, particularly for the production of polyclonal and monoclonal antibodies in laboratory animals, where it is typically used for booster immunizations following a primary dose with its more potent counterpart, Complete Freund's Adjuvant (CFA).[4] Its ability to robustly enhance immunogenicity has also led to its extensive investigation in human clinical trials, primarily as a component of therapeutic cancer vaccines. The clinical development landscape is dominated by early-phase trials in various malignancies, most notably melanoma, where IFA has been used to emulsify tumor-associated peptide antigens, often in combination with checkpoint inhibitors and other immunomodulators.[1]
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
---|---|---|---|---|---|
2025/09/12 | Not Applicable | Not yet recruiting | |||
2023/05/25 | Not Applicable | Recruiting | |||
2021/04/13 | Phase 1 | Completed | |||
2019/07/10 | Phase 2 | Completed | David Peereboom | ||
2019/03/19 | Phase 1 | Completed | |||
2015/05/28 | Phase 2 | Active, not recruiting | |||
2015/01/08 | Phase 1 | Active, not recruiting | |||
2013/04/29 | Phase 1 | Completed | |||
2012/12/12 | Early Phase 1 | Completed | |||
2010/08/06 | 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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