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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2019-01-01
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Online Access: | http://dx.doi.org/10.1080/2331205X.2019.1614286 |
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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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