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VIO-01

Alternative Names: VIO-01, VIO 01, VIO01
Latest Update: 2024-02-14
Latest Update Note: Clinical Trial Update

Product Description

VIO-01 is the second candidate harnessed from Valerio’s propriety platform of DNA decoy therapeutics and is designed to be a next-generation pan-DDR DNA decoy.While PARP inhibitors have been a significant advance in cancer treatment, the class still has several limiting factors, particularly the rapid onset of resistance. As a next-generation pan-DDR DNA decoy, VIO-01 is designed to abrogate several DNA repair pathways and trigger a robust immune response by activating the innate immune response through the STING pathway. The STING pathway plays a critical role in detecting DNA abnormalities and activating the immune system to target and destroy cancer cells. (Sourced from: https://valeriotx.com/our-science/#pipeline)

Mechanisms of Action: PARP Inhibitor

Novel Mechanism: No

Modality: Nucleic Acid

Route of Administration: Intravenous

FDA Designation: None *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Valerio Therapeutics
Company Location:
Company CEO:
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for VIO-01

Countries in Clinic: United States

Active Clinical Trial Count: 1

Highest Development Phases

Phase 2: Breast Cancer|Ovarian Cancer|Prostate Cancer

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

VIO-01-101

P2

Recruiting

Breast Cancer|Ovarian Cancer|Prostate Cancer

2026-01-29

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