Overview
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Indication
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Associated Conditions
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Research Report
Comprehensive Report on the Investigational Drug YYC-506
I. Introduction to YYC-506
YYC-506 is an investigational small molecule pharmaceutical agent, classified as an antihyperlipidemic, currently under development by the South Korean firm Yooyoung Pharm Co. Ltd..[1] The compound has been designated as a New Molecular Entity (NME).[2] The primary therapeutic objective for YYC-506 is the management of complex dyslipidemias. It is specifically being evaluated for patients who have achieved adequate control of their low-density lipoprotein cholesterol (LDL-C) levels through statin therapy, typically with atorvastatin, but continue to exhibit elevated plasma triglycerides (TG) and/or sub-optimal levels of high-density lipoprotein cholesterol (HDL-C).[3] This focus addresses a significant residual cardiovascular risk often observed in patients despite effective LDL-C lowering.
Yooyoung Pharm Co. Ltd. is identified as both the originator and the sole active organization responsible for the clinical development of YYC-506.[1] The drug is currently in the advanced stages of clinical investigation, having reached Phase 3 trials for the treatment of hyperlipidemias in South Korea. Additionally, there are indications of Phase 2 development for dyslipidemias in the United States, suggesting a potential strategy for broader market introduction pending successful trial outcomes.[1]
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
---|---|---|---|---|---|
2021/05/05 | Phase 1 | Completed | Yooyoung Pharmaceutical Co., Ltd. | ||
2021/04/26 | Phase 3 | UNKNOWN | Yooyoung Pharmaceutical Co., Ltd. |
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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