Overview
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Indication
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Associated Conditions
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Research Report
Comprehensive Report on DYV-700/DYV702 for Acute Gout Pain
I. Introduction
DYV-700 is an investigational therapeutic agent formulated as a topical cream for transdermal administration, primarily developed for the management of pain associated with acute gout flares.[1] The development is spearheaded by Dyve Biosciences, Inc., a clinical-stage biotechnology company.[7] It is pertinent to note a nomenclature inconsistency within the source materials; the compound studied in the key clinical trial (NCT04130204) is referred to as both DYV-700 [2] and DYV702.[10] One source clarifies that DYV-700 and DYV-702 are alternative names for a sodium bicarbonate transdermal formulation.[18] This report will use "DYV-700/DYV702" to reflect this ambiguity while acknowledging they likely refer to the same entity. The primary therapeutic goal of DYV-700/DYV702 is to offer rapid pain relief and shorten the duration of acute gout attacks, addressing a significant unmet need in current gout management.[1]
II. Developer Profile: Dyve Biosciences and Technology Platform
Dyve Biosciences is a clinical-stage biotechnology company focusing on leveraging its proprietary transdermal delivery technology, known as the DMAX platform, across various therapeutic areas, including immunology and oncology.[10] A core scientific strategy for the company involves pH modulation, particularly targeting acidic microenvironments associated with disease progression in cancer and inflammatory conditions.[26]
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
---|---|---|---|---|---|
2019/10/17 | Phase 2 | Completed |
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
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No FDA approvals found for this drug. |
EMA Drug Approvals
Approved Product | Authorization Holder | Status | Issued Date |
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No EMA approvals found for this drug. |
HSA Drug Approvals
Approved Product | Manufacturer | Approval Number | Dosage Form | Strength | Approval Date |
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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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