Cargando…
1421. IV Brincidofovir (BCV): Pharmacokinetics (PK) and Safety of Multiple Ascending Doses (MAD) in Healthy Subjects
BACKGROUND: BCV is a lipid conjugated nucleotide analog that has shown rapid viral clearance with oral administration in patients with adenovirus infection, and improved survival in animal models of smallpox. Phase I single ascending dose evaluation of IV BCV demonstrated that 2 hour infusions of 10...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6253859/ http://dx.doi.org/10.1093/ofid/ofy210.1252 |
_version_ | 1783373590730637312 |
---|---|
author | Naderer, Odin Schuck, Virna Morrison, Marion Anderson, Maggie Arumugham, Thangam Dunn, John |
author_facet | Naderer, Odin Schuck, Virna Morrison, Marion Anderson, Maggie Arumugham, Thangam Dunn, John |
author_sort | Naderer, Odin |
collection | PubMed |
description | BACKGROUND: BCV is a lipid conjugated nucleotide analog that has shown rapid viral clearance with oral administration in patients with adenovirus infection, and improved survival in animal models of smallpox. Phase I single ascending dose evaluation of IV BCV demonstrated that 2 hour infusions of 10, 25, and 50 mg were well tolerated and not associated with significant adverse events (AEs) or laboratory abnormalities. This study evaluated the safety and PK of multiple ascending doses of IV BCV in healthy subjects. METHODS: Twenty-eight subjects were to be randomized 3:1 to receive blinded IV BCV or placebo in sequential MAD cohorts (Table A). Study drug was given twice a week (BIW) for 2 weeks or once a week (QW) for 4 weeks. Plasma PK samples were collected on Day 1 and after the last dose and assayed by HPLC-MS. Plasma BCV PK parameters were determined by noncompartmental analysis and dose proportionality and accumulation was assessed. Safety assessments were performed during the dosing period through 14 days post last dose. RESULTS: Twenty-seven male and female subjects (29–65 years, 93% White) were enrolled and 26 completed the study. Plasma BCV C(max) and AUC(∞) increased in proportion to dose with no accumulation (Table A). AEs were generally mild and included diarrhea and headache. Alanine aminotransferase (ALT) elevations were asymptomatic and resolved upon cessation of dosing. No serious AEs occurred. CONCLUSION: Multiple doses of IV BCV given as 10 mg BIW or 20 mg QW were generally safe and well tolerated. Mild diarrhea was reported only after IV BCV 20 mg QW. As seen with oral BCV, ALT increases were reversible upon cessation of drug, and were not associated with hyperbilirubinemia. BCV exposure was dose-proportional and no accumulation was observed. The data support evaluation of repeat dose administration in virally infected patients. DISCLOSURES: O. Naderer, Chimerix: Employee, Salary. V. Schuck, Chimerix: Research Contractor, Consulting fee. M. Morrison, Chimerix: Employee, Salary. M. Anderson, Chimerix: Employee, Salary. T. Arumugham, Chimerix: Employee, Salary. J. Dunn, Chimerix: Employee, Salary. |
format | Online Article Text |
id | pubmed-6253859 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-62538592018-11-28 1421. IV Brincidofovir (BCV): Pharmacokinetics (PK) and Safety of Multiple Ascending Doses (MAD) in Healthy Subjects Naderer, Odin Schuck, Virna Morrison, Marion Anderson, Maggie Arumugham, Thangam Dunn, John Open Forum Infect Dis Abstracts BACKGROUND: BCV is a lipid conjugated nucleotide analog that has shown rapid viral clearance with oral administration in patients with adenovirus infection, and improved survival in animal models of smallpox. Phase I single ascending dose evaluation of IV BCV demonstrated that 2 hour infusions of 10, 25, and 50 mg were well tolerated and not associated with significant adverse events (AEs) or laboratory abnormalities. This study evaluated the safety and PK of multiple ascending doses of IV BCV in healthy subjects. METHODS: Twenty-eight subjects were to be randomized 3:1 to receive blinded IV BCV or placebo in sequential MAD cohorts (Table A). Study drug was given twice a week (BIW) for 2 weeks or once a week (QW) for 4 weeks. Plasma PK samples were collected on Day 1 and after the last dose and assayed by HPLC-MS. Plasma BCV PK parameters were determined by noncompartmental analysis and dose proportionality and accumulation was assessed. Safety assessments were performed during the dosing period through 14 days post last dose. RESULTS: Twenty-seven male and female subjects (29–65 years, 93% White) were enrolled and 26 completed the study. Plasma BCV C(max) and AUC(∞) increased in proportion to dose with no accumulation (Table A). AEs were generally mild and included diarrhea and headache. Alanine aminotransferase (ALT) elevations were asymptomatic and resolved upon cessation of dosing. No serious AEs occurred. CONCLUSION: Multiple doses of IV BCV given as 10 mg BIW or 20 mg QW were generally safe and well tolerated. Mild diarrhea was reported only after IV BCV 20 mg QW. As seen with oral BCV, ALT increases were reversible upon cessation of drug, and were not associated with hyperbilirubinemia. BCV exposure was dose-proportional and no accumulation was observed. The data support evaluation of repeat dose administration in virally infected patients. DISCLOSURES: O. Naderer, Chimerix: Employee, Salary. V. Schuck, Chimerix: Research Contractor, Consulting fee. M. Morrison, Chimerix: Employee, Salary. M. Anderson, Chimerix: Employee, Salary. T. Arumugham, Chimerix: Employee, Salary. J. Dunn, Chimerix: Employee, Salary. Oxford University Press 2018-11-26 /pmc/articles/PMC6253859/ http://dx.doi.org/10.1093/ofid/ofy210.1252 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Abstracts Naderer, Odin Schuck, Virna Morrison, Marion Anderson, Maggie Arumugham, Thangam Dunn, John 1421. IV Brincidofovir (BCV): Pharmacokinetics (PK) and Safety of Multiple Ascending Doses (MAD) in Healthy Subjects |
title | 1421. IV Brincidofovir (BCV): Pharmacokinetics (PK) and Safety of Multiple Ascending Doses (MAD) in Healthy Subjects |
title_full | 1421. IV Brincidofovir (BCV): Pharmacokinetics (PK) and Safety of Multiple Ascending Doses (MAD) in Healthy Subjects |
title_fullStr | 1421. IV Brincidofovir (BCV): Pharmacokinetics (PK) and Safety of Multiple Ascending Doses (MAD) in Healthy Subjects |
title_full_unstemmed | 1421. IV Brincidofovir (BCV): Pharmacokinetics (PK) and Safety of Multiple Ascending Doses (MAD) in Healthy Subjects |
title_short | 1421. IV Brincidofovir (BCV): Pharmacokinetics (PK) and Safety of Multiple Ascending Doses (MAD) in Healthy Subjects |
title_sort | 1421. iv brincidofovir (bcv): pharmacokinetics (pk) and safety of multiple ascending doses (mad) in healthy subjects |
topic | Abstracts |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6253859/ http://dx.doi.org/10.1093/ofid/ofy210.1252 |
work_keys_str_mv | AT nadererodin 1421ivbrincidofovirbcvpharmacokineticspkandsafetyofmultipleascendingdosesmadinhealthysubjects AT schuckvirna 1421ivbrincidofovirbcvpharmacokineticspkandsafetyofmultipleascendingdosesmadinhealthysubjects AT morrisonmarion 1421ivbrincidofovirbcvpharmacokineticspkandsafetyofmultipleascendingdosesmadinhealthysubjects AT andersonmaggie 1421ivbrincidofovirbcvpharmacokineticspkandsafetyofmultipleascendingdosesmadinhealthysubjects AT arumughamthangam 1421ivbrincidofovirbcvpharmacokineticspkandsafetyofmultipleascendingdosesmadinhealthysubjects AT dunnjohn 1421ivbrincidofovirbcvpharmacokineticspkandsafetyofmultipleascendingdosesmadinhealthysubjects |