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Brincidofovir

Alternative Names: brincidofovir, cmx001, TEMBEXA, cmx-001, SYB V-1901, SYBV-1901
Latest Update: 2024-12-04
Latest Update Note: Clinical Trial Update

Product Description

Brincidofovir is an alkoxyalkyl ester prodrug containing the synthetic, acyclic nucleoside monophosphate analog cidofovir linked, through its phosphonate group, to a lipid, 3-hexadecyloxy-1-propanol, with antiviral activity against double-stranded DNA viruses. Upon oral administration, brincidofovir crosses the intestinal wall and penetrates target viral-infected cells before being cleaved to the free antiviral agent cidofovir. (Sourced from: https://pubchem.ncbi.nlm.nih.gov/compound/Brincidofovir)

Mechanisms of Action: DNA Polymerase Inhibitor

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: Intravenous,Oral

FDA Designation: None *

Approval Status: Approved

Approved Countries: United States

Approved Indications: Smallpox

Known Adverse Events: Abdominal Pain | Pain Unspecified | Diarrhea

Company: Chimerix
Company Location: DURHAM NC 27713
Company CEO: Michael A. Sherman
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Brincidofovir

Countries in Clinic: Australia, South Korea, United States

Active Clinical Trial Count: 5

Highest Development Phases

Phase 2: Kidney Transplant

Phase 1: Papilloma|Smallpox

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

jRCT2041220056

P2

Recruiting

Kidney Transplant

2024-12-31

BCV-001

P1

Completed

Smallpox

2023-08-14

70%

ACTRN12618002011268

P1

Not yet recruiting

Papilloma

2019-03-29

ACTRN12616001657415

P1

Recruiting

Smallpox

2017-03-17

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