Overview
Vidutolimod is a Toll-like receptor 9 (TLR9) agonist. It is an investigational cancer vaccine.
Indication
No indication information available.
Associated Conditions
No associated conditions information available.
Research Report
Vidutolimod (DB17500): An Investigational TLR9 Agonist Cancer Vaccine
1.0 Introduction
1.1 Overview of Vidutolimod
Vidutolimod (DrugBank ID: DB17500) is an investigational biotechnology product classified as a Toll-like receptor 9 (TLR9) agonist, being developed as a potential cancer vaccine.[1] It is also known by several alternative names and codes, including CMP-001, CYT-003, CYT003-QbG10, QbG10, and ARB 1598.[1] The core therapeutic strategy behind Vidutolimod involves harnessing the patient's own innate and adaptive immune systems to recognize and combat malignant cells.[3] It is designed for intratumoral administration, aiming to activate local immune responses that translate into systemic anti-tumor immunity.[4]
1.2 Therapeutic Context
The development of TLR9 agonists like Vidutolimod stems from the need to enhance the efficacy of cancer immunotherapy. While immune checkpoint inhibitors (ICIs), particularly those targeting the PD-1/PD-L1 axis, have revolutionized cancer treatment, a significant proportion of patients either do not respond initially (primary resistance) or develop resistance after an initial response (acquired resistance).[8] Vidutolimod aims to address this limitation by activating the innate immune system, specifically plasmacytoid dendritic cells (pDCs), through TLR9 stimulation.[5] Activation of pDCs leads to the production of Type I interferons (IFNs), which play a critical role in bridging innate and adaptive immunity, promoting the maturation of antigen-presenting cells, and ultimately driving the generation and recruitment of tumor-specific cytotoxic T lymphocytes (CTLs).[5] By converting immunologically "cold" or non-inflamed tumors into "hot," T-cell-inflamed environments, intratumoral TLR9 agonists like Vidutolimod are hypothesized to overcome resistance to ICIs and improve patient outcomes.[5]
1.3 Scope of Report
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
---|---|---|---|---|---|
2023/10/03 | N/A | NO_LONGER_AVAILABLE | |||
2021/06/07 | Phase 2 | Terminated | |||
2021/03/19 | Phase 2 | Active, not recruiting | |||
2021/01/06 | Phase 2 | Terminated | |||
2021/01/06 | Phase 2 | Terminated | |||
2020/11/18 | Phase 2 | Terminated | |||
2020/05/26 | Phase 2 | Completed | Diwakar Davar | ||
2019/06/12 | Phase 1 | Completed | Umar Farooq | ||
2018/08/07 | Phase 2 | Completed | Diwakar Davar | ||
2018/04/25 | Phase 1 | 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. |
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