Breakthrough hope for rare brain disease as major drug trial begins
NCT ID NCT07185347
Summary
This study is testing whether a drug called fampridine can improve movement control and vision problems in people with a specific genetic brain condition called SCA27B. It will involve 70 adults who have this condition. For 3 months, half will receive the real drug and half a placebo pill, and researchers will carefully measure changes in walking, balance, and daily activities.
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Contacts and locations
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Study contacts
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Contact
Email: •••••@•••••
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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Genetics Department, CHU de Bordeaux
RECRUITINGBordeaux, France
Contact
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Genetics Department, CHU de Rouen
NOT_YET_RECRUITINGRouen, France
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Genetics Department, Pitié-Salpêtrière University Hospital
RECRUITINGParis, France
Contact Phone: •••-•••-•••• Email: •••••@•••••
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Neurology Department, CHRU de Strasbourg
NOT_YET_RECRUITINGStrasbourg, France
Contact
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Neurology Department, CHU d'Angers
NOT_YET_RECRUITINGAngers, France
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Neurology Department, CHU de Toulouse
NOT_YET_RECRUITINGToulouse, France
Contact
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Neurology Department, Gui De Chauliac Hospital
RECRUITINGMontpellier, France
Contact
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Neurology Department, Hôpital Pierre Wertheimer Hospital
NOT_YET_RECRUITINGLyon, France
Contact
Contact
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Neurology and Gentics Department, CHU de Dijon
RECRUITINGDijon, France
Contact
Conditions
Explore the condition pages connected to this study.