Overview
Adrabetadex is under investigation in clinical trial NCT03887533 (Combined Intrathecal and Intravenous VTS-270 Therapy for Liver and Neurological Disease Associated With Niemann-Pick Disease, Type C1).
Indication
No indication information available.
Associated Conditions
No associated conditions information available.
Research Report
Adrabetadex (VTS-270): A Comprehensive Review of its Development for Niemann-Pick Disease Type C1
I. Introduction to Adrabetadex (VTS-270)
A. Overview of the Compound
Adrabetadex represents an investigational therapeutic agent developed primarily for Niemann-Pick Disease Type C (NPC). It is the United States Adopted Name (USAN) for a specific formulation of (2-hydroxypropyl)-β-cyclodextrin (HPβCD).[1] HPβCD is a chemically modified cyclic oligosaccharide derived from β-cyclodextrin, belonging to the chemical class of beta-cyclodextrins and ethers.[2] Although classified as a small molecule for regulatory and database purposes [4], HPβCD itself is not a single molecular entity but rather a complex mixture of β-cyclodextrin molecules with varying degrees of hydroxypropylation.[3] The specific formulation investigated extensively in clinical trials for NPC was designated VTS-270.[3] Other identifiers associated with this substance include Kleptose HPB.[1] The development and nomenclature history reflect its transition from a chemical entity (HPβCD) to a specific investigational drug product (VTS-270) and finally to a formally adopted name (Adrabetadex).
B. Identification and Properties
Precise identification is crucial for tracking and researching this investigational compound. Key identifiers and basic properties are summarized in Table 1.
Table 1: Adrabetadex Key Identifiers and Properties
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
---|---|---|---|---|---|
2024/07/05 | Phase 2 | Recruiting | |||
2021/07/12 | Phase 2 | Terminated | |||
2019/03/25 | Phase 1 | Terminated | Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) | ||
2019/03/19 | Phase 2 | Terminated | |||
2018/09/27 | Phase 2 | Withdrawn | Vtesse, LLC, a Mallinckrodt Pharmaceuticals Company | ||
2018/08/23 | Phase 3 | Terminated | |||
2018/03/20 | Phase 1 | Completed | |||
2015/08/28 | Phase 2 | Completed | |||
2012/12/11 | Phase 1 | Completed | Vtesse, LLC, a Mallinckrodt Pharmaceuticals Company |
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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