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Vosaroxin

Alternative Names: vosaroxin, voreloxin, sns-595
Latest Update: 2024-08-07
Latest Update Note: Clinical Trial Update

Product Description

A small molecule and a naphthyridine analogue with antineoplastic activity. Vosaroxin intercalates into DNA in a site-specific manner and blocks the re-ligation process carried out by topoisomerase II during DNA replication. As a result, inhibition of DNA replication, RNA and protein synthesis occurs, followed by cell cycle arrest at G2 phase and induced p53-independent apoptosis. This agent shows a favorable toxicity profile in several aspects: it does not generate reactive oxygen species, as do anthracyclines, hence reducing the risk of cardiotoxicity; it is not a P-glycoprotein (P-gp) substrate, and thereby evades the common mechanism for multidrug resistance; and it has limited distribution to normal tissues and a more chemically stable molecular structure. (Sourced from: https://www.cancer.gov/publications/dictionaries/cancer-drug/def/vosaroxin)

Mechanisms of Action: TOP Inhibitor

Novel Mechanism: Yes

Modality: Small Molecule

Route of Administration: Intravenous

FDA Designation: None *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

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

Clinical Description

Map of Global Clinical Trials for Vosaroxin

Countries in Clinic:

Active Clinical Trial Count:

Highest Development Phases

Phase 3: Acute Myeloid Leukemia

Phase 2: Acute Lymphoid Leukemia|Acute Myeloid Leukemia|Myelodysplastic Syndrome|Preleukemia|Small Cell Lung Cancer|Non-Small-Cell Lung Cancer|Sarcoma, Myeloid|Ovarian Cancer|Anemia, Refractory, with Excess of Blasts

Phase 1: Oncology Solid Tumor Unspecified|Myelogenous, Chronic, BCR-ABL Positive Leukemia|Acute Lymphoid Leukemia|Myelodysplastic Syndrome|Acute Myeloid Leukemia|Precursor Cell Lymphoblastic Leukemia-Lymphoma|Preleukemia|Chronic Myeloid Leukemia|Chronic Lymphoid Leukemia

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

NCI-2013-01665

P2

Completed

Acute Myeloid Leukemia|Myelodysplastic Syndrome|Preleukemia

2021-01-11

AMLSG 24-15

P2

Completed

Myelodysplastic Syndrome|Preleukemia|Acute Myeloid Leukemia|Anemia, Refractory, with Excess of Blasts

2019-10-31

AMLSG 24-15

P2

Terminated

Myelodysplastic Syndrome|Acute Myeloid Leukemia

2019-10-31

VITAL

P2

Active, not recruiting

Preleukemia|Acute Myeloid Leukemia|Sarcoma, Myeloid|Myelodysplastic Syndrome

2019-04-01

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