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CF33-hNIS

Alternative Names: CF33-hNIS, Vaxinia, CF33hNIS
Latest Update: 2024-12-31
Latest Update Note: Clinical Trial Update

Product Description

CF33-hNIS-antiPDL1 is a genetically engineered chimeric orthopoxvirus, CF33, armed with the human Sodium Iodide Symporter (hNIS) and anti-PD-L1 antibody (anti-PD-L1). (Sourced from: https://pubmed.ncbi.nlm.nih.gov/32032721/)

Mechanisms of Action: PD-L1 Inhibitor

Novel Mechanism: No

Modality: Antibody

Route of Administration: Intramuscular,Intravenous

FDA Designation: None *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Imugene
Company Location:
Company CEO:
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for CF33-hNIS

Countries in Clinic: Australia, United States

Active Clinical Trial Count: 2

Highest Development Phases

Phase 1: Bile Duct Cancer|Cholangiocarcinoma|Triple Negative Breast Cancer

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

NCI-2021-08983

P1

Active, not recruiting

Triple Negative Breast Cancer

2025-06-22

MAST

P1

Recruiting

Cholangiocarcinoma|Bile Duct Cancer

2024-12-01

27%

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