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Cenicriviroc

Alternative Names: cenicriviroc, tbr-652
Latest Update: 2025-01-06
Latest Update Note: News Article

Product Description

Cenicriviroc (CVC) is a novel, orally administered, potent chemokine 2 and 5 receptor antagonist currently in development for the treatment of liver fibrosis in adults with NASH. (Sourced from: https://pubmed.ncbi.nlm.nih.gov/31881392/)

Mechanisms of Action: CCR2 Antagonist,CCR5 Antagonist,Immunomodulator

Novel Mechanism: Yes

Modality: Small Molecule

Route of Administration: Oral

FDA Designation: None *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Tobira
Company Location: SOUTH SAN FRANCISCO CA 94080
Company CEO:
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Cenicriviroc

Countries in Clinic:

Active Clinical Trial Count: 1

Highest Development Phases

Phase 2: Hepatitis, Alcoholic|Liver Cirrhosis|Non-alcoholic Steatohepatitis

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

2016-004754-15

P2

Unknown status

Hepatitis, Alcoholic|Non-alcoholic Steatohepatitis|Liver Cirrhosis

2027-06-05

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