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MULTICENTRE DOUBLE-BLIND STUDY OF EFFECT OF INTRATHECALLY ADMINISTERED NATURAL HUMAN FIBROBLAST INTERFERON ON EXACERBATIONS OF MULTIPLE SCLEROSIS()

In this randomised, double-blind, placebo-controlled, 2-year multicentre study intrathecally administered natural human fibroblast interferon (IFN-B) was effective in reducing exacerbations of multiple sclerosis (MS) in patients with exacerbating/remitting disease. The mean reduction in exacerbation...

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Autores principales: Jacobs, Lawrence, Herndon, Robert, Freeman, Arnold, Cuetter, Albert, Smith, WilliamA., Salazar, AndresM., Reese, PeterA., Josefowicz, Ralph, Husain, Farhat, Ekes, Roslyn, O'Malley, JudithA.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Published by Elsevier Ltd. 1986
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7134842/
https://www.ncbi.nlm.nih.gov/pubmed/2878272
http://dx.doi.org/10.1016/S0140-6736(86)92730-3
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author Jacobs, Lawrence
Herndon, Robert
Freeman, Arnold
Cuetter, Albert
Smith, WilliamA.
Salazar, AndresM.
Reese, PeterA.
Josefowicz, Ralph
Husain, Farhat
Ekes, Roslyn
O'Malley, JudithA.
author_facet Jacobs, Lawrence
Herndon, Robert
Freeman, Arnold
Cuetter, Albert
Smith, WilliamA.
Salazar, AndresM.
Reese, PeterA.
Josefowicz, Ralph
Husain, Farhat
Ekes, Roslyn
O'Malley, JudithA.
author_sort Jacobs, Lawrence
collection PubMed
description In this randomised, double-blind, placebo-controlled, 2-year multicentre study intrathecally administered natural human fibroblast interferon (IFN-B) was effective in reducing exacerbations of multiple sclerosis (MS) in patients with exacerbating/remitting disease. The mean reduction in exacerbation rate of 34 patients who received IFN-B (recipients) was significantly greater during the study than that of 35 patients who received placebo (p <0.04). The prestudy exacerbation rates were comparable in recipients and controls, but the rate at the end of the study was significantly lower in recipients than in controls (p <0.001). IFN-B was given by nine or ten lumbar punctures over the first 6 months of the study, and patient observations continued for 2 years. IFN-B was well tolerated in 95% of the recipients, and the side-effects experienced were clearly acceptable for the benefits achieved. Low doses of indomethacin reduced the toxicity of IFN-B and played an important role in successful double-blinding.
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spelling pubmed-71348422020-04-08 MULTICENTRE DOUBLE-BLIND STUDY OF EFFECT OF INTRATHECALLY ADMINISTERED NATURAL HUMAN FIBROBLAST INTERFERON ON EXACERBATIONS OF MULTIPLE SCLEROSIS() Jacobs, Lawrence Herndon, Robert Freeman, Arnold Cuetter, Albert Smith, WilliamA. Salazar, AndresM. Reese, PeterA. Josefowicz, Ralph Husain, Farhat Ekes, Roslyn O'Malley, JudithA. Lancet Article In this randomised, double-blind, placebo-controlled, 2-year multicentre study intrathecally administered natural human fibroblast interferon (IFN-B) was effective in reducing exacerbations of multiple sclerosis (MS) in patients with exacerbating/remitting disease. The mean reduction in exacerbation rate of 34 patients who received IFN-B (recipients) was significantly greater during the study than that of 35 patients who received placebo (p <0.04). The prestudy exacerbation rates were comparable in recipients and controls, but the rate at the end of the study was significantly lower in recipients than in controls (p <0.001). IFN-B was given by nine or ten lumbar punctures over the first 6 months of the study, and patient observations continued for 2 years. IFN-B was well tolerated in 95% of the recipients, and the side-effects experienced were clearly acceptable for the benefits achieved. Low doses of indomethacin reduced the toxicity of IFN-B and played an important role in successful double-blinding. Published by Elsevier Ltd. 1986-12-27 2003-10-28 /pmc/articles/PMC7134842/ /pubmed/2878272 http://dx.doi.org/10.1016/S0140-6736(86)92730-3 Text en Copyright © 1986 Published by Elsevier Ltd. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Jacobs, Lawrence
Herndon, Robert
Freeman, Arnold
Cuetter, Albert
Smith, WilliamA.
Salazar, AndresM.
Reese, PeterA.
Josefowicz, Ralph
Husain, Farhat
Ekes, Roslyn
O'Malley, JudithA.
MULTICENTRE DOUBLE-BLIND STUDY OF EFFECT OF INTRATHECALLY ADMINISTERED NATURAL HUMAN FIBROBLAST INTERFERON ON EXACERBATIONS OF MULTIPLE SCLEROSIS()
title MULTICENTRE DOUBLE-BLIND STUDY OF EFFECT OF INTRATHECALLY ADMINISTERED NATURAL HUMAN FIBROBLAST INTERFERON ON EXACERBATIONS OF MULTIPLE SCLEROSIS()
title_full MULTICENTRE DOUBLE-BLIND STUDY OF EFFECT OF INTRATHECALLY ADMINISTERED NATURAL HUMAN FIBROBLAST INTERFERON ON EXACERBATIONS OF MULTIPLE SCLEROSIS()
title_fullStr MULTICENTRE DOUBLE-BLIND STUDY OF EFFECT OF INTRATHECALLY ADMINISTERED NATURAL HUMAN FIBROBLAST INTERFERON ON EXACERBATIONS OF MULTIPLE SCLEROSIS()
title_full_unstemmed MULTICENTRE DOUBLE-BLIND STUDY OF EFFECT OF INTRATHECALLY ADMINISTERED NATURAL HUMAN FIBROBLAST INTERFERON ON EXACERBATIONS OF MULTIPLE SCLEROSIS()
title_short MULTICENTRE DOUBLE-BLIND STUDY OF EFFECT OF INTRATHECALLY ADMINISTERED NATURAL HUMAN FIBROBLAST INTERFERON ON EXACERBATIONS OF MULTIPLE SCLEROSIS()
title_sort multicentre double-blind study of effect of intrathecally administered natural human fibroblast interferon on exacerbations of multiple sclerosis()
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7134842/
https://www.ncbi.nlm.nih.gov/pubmed/2878272
http://dx.doi.org/10.1016/S0140-6736(86)92730-3
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