Clinical Tests Testing New Therapies for Stargardt Disease
To provide information on currently ongoing clinical trials for Stargardt disease. We have searched the clinical trial register (www.clinicaltrials.gov) for the keyword "Stargardt" and list active ongoing studies. There are currently eight registered clinical trials enrolling patients with...
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Veröffentlicht in: | Česká a slovenská oftalmologie 2016-02, Vol.72 (1), p.293-297 |
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creator | Kousal, B Ďuďáková, Ľ Hlavatá, L Lišková, P |
description | To provide information on currently ongoing clinical trials for Stargardt disease.
We have searched the clinical trial register (www.clinicaltrials.gov) for the keyword "Stargardt" and list active ongoing studies.
There are currently eight registered clinical trials enrolling patients with Stargardt disease; all in phase I or II aiming at four mechanisms of action: inhibition of the production of vitamin A toxic dimers, gene therapy restoring wild type transcription of the ABCA4 gene, neuroprotection preventing retinal cells from oxidative damage, and replacement of the damaged retinal pigment epithelium using stem cell therapy. The basic prerequisite for enrolment in the vast majority of clinical trials is confirmation of the clinical diagnosis by mutational analysis.
The wide variety of therapies that are registered as clinical trials for Stargardt disease significantly raises the possibility that effective treatments will be available in the near future for this currently incurable condition and that molecular genetic testing should be increasingly considered.
Stargardt disease, clinical trial, ABCA4, mutation. |
format | Article |
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We have searched the clinical trial register (www.clinicaltrials.gov) for the keyword "Stargardt" and list active ongoing studies.
There are currently eight registered clinical trials enrolling patients with Stargardt disease; all in phase I or II aiming at four mechanisms of action: inhibition of the production of vitamin A toxic dimers, gene therapy restoring wild type transcription of the ABCA4 gene, neuroprotection preventing retinal cells from oxidative damage, and replacement of the damaged retinal pigment epithelium using stem cell therapy. The basic prerequisite for enrolment in the vast majority of clinical trials is confirmation of the clinical diagnosis by mutational analysis.
The wide variety of therapies that are registered as clinical trials for Stargardt disease significantly raises the possibility that effective treatments will be available in the near future for this currently incurable condition and that molecular genetic testing should be increasingly considered.
Stargardt disease, clinical trial, ABCA4, mutation.</description><identifier>ISSN: 1211-9059</identifier><identifier>PMID: 27041285</identifier><language>cze</language><publisher>Czech Republic</publisher><subject>ATP-Binding Cassette Transporters - genetics ; Cell- and Tissue-Based Therapy ; Clinical Trials as Topic ; DNA Mutational Analysis ; Female ; Genetic Therapy ; Genotype ; Humans ; Macular Degeneration - congenital ; Macular Degeneration - diagnosis ; Macular Degeneration - genetics ; Macular Degeneration - therapy ; Male ; Mutation ; Retinal Pigment Epithelium - pathology ; Stem Cell Transplantation</subject><ispartof>Česká a slovenská oftalmologie, 2016-02, Vol.72 (1), p.293-297</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27041285$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kousal, B</creatorcontrib><creatorcontrib>Ďuďáková, Ľ</creatorcontrib><creatorcontrib>Hlavatá, L</creatorcontrib><creatorcontrib>Lišková, P</creatorcontrib><title>Clinical Tests Testing New Therapies for Stargardt Disease</title><title>Česká a slovenská oftalmologie</title><addtitle>Cesk Slov Oftalmol</addtitle><description>To provide information on currently ongoing clinical trials for Stargardt disease.
We have searched the clinical trial register (www.clinicaltrials.gov) for the keyword "Stargardt" and list active ongoing studies.
There are currently eight registered clinical trials enrolling patients with Stargardt disease; all in phase I or II aiming at four mechanisms of action: inhibition of the production of vitamin A toxic dimers, gene therapy restoring wild type transcription of the ABCA4 gene, neuroprotection preventing retinal cells from oxidative damage, and replacement of the damaged retinal pigment epithelium using stem cell therapy. The basic prerequisite for enrolment in the vast majority of clinical trials is confirmation of the clinical diagnosis by mutational analysis.
The wide variety of therapies that are registered as clinical trials for Stargardt disease significantly raises the possibility that effective treatments will be available in the near future for this currently incurable condition and that molecular genetic testing should be increasingly considered.
Stargardt disease, clinical trial, ABCA4, mutation.</description><subject>ATP-Binding Cassette Transporters - genetics</subject><subject>Cell- and Tissue-Based Therapy</subject><subject>Clinical Trials as Topic</subject><subject>DNA Mutational Analysis</subject><subject>Female</subject><subject>Genetic Therapy</subject><subject>Genotype</subject><subject>Humans</subject><subject>Macular Degeneration - congenital</subject><subject>Macular Degeneration - diagnosis</subject><subject>Macular Degeneration - genetics</subject><subject>Macular Degeneration - therapy</subject><subject>Male</subject><subject>Mutation</subject><subject>Retinal Pigment Epithelium - pathology</subject><subject>Stem Cell Transplantation</subject><issn>1211-9059</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo1T8lOwzAU9AFEq9JfQD5yifQcx0u4obBVquBA7tFL_FKM0iTYiRB_T4BymZFGo1nO2FqkQiQ5qHzFtjG-A4AAq7SQF2yVGshEatWa3RSd732DHS8pTvEXfX_gz_TJyzcKOHqKvB0Cf50wHDC4id_5SBjpkp232EXannjDyof7snhK9i-Pu-J2n4xKq0TbWrU16Nop5yxmtZICmqU9UwgmRb0IgDlAniORNFKnUjvdgoUfaOSGXf_FjmH4mJd51dHHhroOexrmWAljrAGjlV2sVyfrXB_JVWPwRwxf1f9d-Q2VSE7T</recordid><startdate>201602</startdate><enddate>201602</enddate><creator>Kousal, B</creator><creator>Ďuďáková, Ľ</creator><creator>Hlavatá, L</creator><creator>Lišková, P</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>201602</creationdate><title>Clinical Tests Testing New Therapies for Stargardt Disease</title><author>Kousal, B ; Ďuďáková, Ľ ; Hlavatá, L ; Lišková, P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p565-68b5fb06bd5dd8a4b5310c41245a072a6b530a90099aee3736236d6f0806f08c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>cze</language><creationdate>2016</creationdate><topic>ATP-Binding Cassette Transporters - genetics</topic><topic>Cell- and Tissue-Based Therapy</topic><topic>Clinical Trials as Topic</topic><topic>DNA Mutational Analysis</topic><topic>Female</topic><topic>Genetic Therapy</topic><topic>Genotype</topic><topic>Humans</topic><topic>Macular Degeneration - congenital</topic><topic>Macular Degeneration - diagnosis</topic><topic>Macular Degeneration - genetics</topic><topic>Macular Degeneration - therapy</topic><topic>Male</topic><topic>Mutation</topic><topic>Retinal Pigment Epithelium - pathology</topic><topic>Stem Cell Transplantation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kousal, B</creatorcontrib><creatorcontrib>Ďuďáková, Ľ</creatorcontrib><creatorcontrib>Hlavatá, L</creatorcontrib><creatorcontrib>Lišková, P</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Česká a slovenská oftalmologie</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kousal, B</au><au>Ďuďáková, Ľ</au><au>Hlavatá, L</au><au>Lišková, P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Clinical Tests Testing New Therapies for Stargardt Disease</atitle><jtitle>Česká a slovenská oftalmologie</jtitle><addtitle>Cesk Slov Oftalmol</addtitle><date>2016-02</date><risdate>2016</risdate><volume>72</volume><issue>1</issue><spage>293</spage><epage>297</epage><pages>293-297</pages><issn>1211-9059</issn><abstract>To provide information on currently ongoing clinical trials for Stargardt disease.
We have searched the clinical trial register (www.clinicaltrials.gov) for the keyword "Stargardt" and list active ongoing studies.
There are currently eight registered clinical trials enrolling patients with Stargardt disease; all in phase I or II aiming at four mechanisms of action: inhibition of the production of vitamin A toxic dimers, gene therapy restoring wild type transcription of the ABCA4 gene, neuroprotection preventing retinal cells from oxidative damage, and replacement of the damaged retinal pigment epithelium using stem cell therapy. The basic prerequisite for enrolment in the vast majority of clinical trials is confirmation of the clinical diagnosis by mutational analysis.
The wide variety of therapies that are registered as clinical trials for Stargardt disease significantly raises the possibility that effective treatments will be available in the near future for this currently incurable condition and that molecular genetic testing should be increasingly considered.
Stargardt disease, clinical trial, ABCA4, mutation.</abstract><cop>Czech Republic</cop><pmid>27041285</pmid><tpages>5</tpages></addata></record> |
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subjects | ATP-Binding Cassette Transporters - genetics Cell- and Tissue-Based Therapy Clinical Trials as Topic DNA Mutational Analysis Female Genetic Therapy Genotype Humans Macular Degeneration - congenital Macular Degeneration - diagnosis Macular Degeneration - genetics Macular Degeneration - therapy Male Mutation Retinal Pigment Epithelium - pathology Stem Cell Transplantation |
title | Clinical Tests Testing New Therapies for Stargardt Disease |
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