A controlled clinical trial of ultraviolet blood irradiation (UVBI) for hepatitis C infection

The FDA Phase I controlled clinical trial results of ultraviolet blood irradiation (UVBI) to treat patients with hepatitis C Virus (HCV) infection are described in this report. This study was conducted prior to the availability of other highly effective therapies, e.g., the combination of ledipasvir...

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Main Authors: J. Todd Kuenstner, Shanker Mukherjee, Zachary Schafer, William Kuenstner, Thomas Petrie
Format: Article
Language:English
Published: Taylor & Francis Group 2019-01-01
Series:Cogent Medicine
Subjects:
Online Access:http://dx.doi.org/10.1080/2331205X.2019.1614286
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spelling doaj-a413ca42aa364d8690a3496c5de8c5b32021-03-18T15:12:52ZengTaylor & Francis GroupCogent Medicine2331-205X2019-01-016110.1080/2331205X.2019.16142861614286A controlled clinical trial of ultraviolet blood irradiation (UVBI) for hepatitis C infectionJ. Todd Kuenstner0Shanker Mukherjee1Zachary Schafer2William Kuenstner3Thomas Petrie4Temple University HospitalTwin Rivers Gastroenterology CenterNorth Carolina State Center for Health Statistics, Division of Public HealthWest Virginia University School of MedicineAVIcure Bioscience, LLCThe FDA Phase I controlled clinical trial results of ultraviolet blood irradiation (UVBI) to treat patients with hepatitis C Virus (HCV) infection are described in this report. This study was conducted prior to the availability of other highly effective therapies, e.g., the combination of ledipasvir and sofosbuvir (Gilead Sciences, Inc.). Five UVBI treatments were administered to 10 patients in 3 weeks. Viral loads and markers of hepatic inflammation were assessed before and after treatment. The patients were treated with a modified Knott Hemo-Irradiator (AVIcure Bioscience, LLC). After five treatments in nine of the patients, the mean percentage change in viral load was −56.0% and the mean change in log viral load was −0.60 (p = 0.017). During the study, seven of 10 patients demonstrated a > 0.49 log reduction in viral load. There were no significant adverse events. UVBI was safe in all patients and effective for the treatment of HCV infection in a majority of patients (IDE #G030242). This device should be studied for the treatment of other infectious diseases for which there are few treatment options.http://dx.doi.org/10.1080/2331205X.2019.1614286ultraviolet blood irradiationcrohn’s diseasetuberculosishepatitis c virus
collection DOAJ
language English
format Article
sources DOAJ
author J. Todd Kuenstner
Shanker Mukherjee
Zachary Schafer
William Kuenstner
Thomas Petrie
spellingShingle J. Todd Kuenstner
Shanker Mukherjee
Zachary Schafer
William Kuenstner
Thomas Petrie
A controlled clinical trial of ultraviolet blood irradiation (UVBI) for hepatitis C infection
Cogent Medicine
ultraviolet blood irradiation
crohn’s disease
tuberculosis
hepatitis c virus
author_facet J. Todd Kuenstner
Shanker Mukherjee
Zachary Schafer
William Kuenstner
Thomas Petrie
author_sort J. Todd Kuenstner
title A controlled clinical trial of ultraviolet blood irradiation (UVBI) for hepatitis C infection
title_short A controlled clinical trial of ultraviolet blood irradiation (UVBI) for hepatitis C infection
title_full A controlled clinical trial of ultraviolet blood irradiation (UVBI) for hepatitis C infection
title_fullStr A controlled clinical trial of ultraviolet blood irradiation (UVBI) for hepatitis C infection
title_full_unstemmed A controlled clinical trial of ultraviolet blood irradiation (UVBI) for hepatitis C infection
title_sort controlled clinical trial of ultraviolet blood irradiation (uvbi) for hepatitis c infection
publisher Taylor & Francis Group
series Cogent Medicine
issn 2331-205X
publishDate 2019-01-01
description The FDA Phase I controlled clinical trial results of ultraviolet blood irradiation (UVBI) to treat patients with hepatitis C Virus (HCV) infection are described in this report. This study was conducted prior to the availability of other highly effective therapies, e.g., the combination of ledipasvir and sofosbuvir (Gilead Sciences, Inc.). Five UVBI treatments were administered to 10 patients in 3 weeks. Viral loads and markers of hepatic inflammation were assessed before and after treatment. The patients were treated with a modified Knott Hemo-Irradiator (AVIcure Bioscience, LLC). After five treatments in nine of the patients, the mean percentage change in viral load was −56.0% and the mean change in log viral load was −0.60 (p = 0.017). During the study, seven of 10 patients demonstrated a > 0.49 log reduction in viral load. There were no significant adverse events. UVBI was safe in all patients and effective for the treatment of HCV infection in a majority of patients (IDE #G030242). This device should be studied for the treatment of other infectious diseases for which there are few treatment options.
topic ultraviolet blood irradiation
crohn’s disease
tuberculosis
hepatitis c virus
url http://dx.doi.org/10.1080/2331205X.2019.1614286
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