Saccadic Eye Movements in Patients With Niemann-Pick Type C Disease
Status: | Completed |
---|---|
Conditions: | Neurology, Neurology |
Therapuetic Areas: | Neurology |
Healthy: | No |
Age Range: | 12 - Any |
Updated: | 4/21/2016 |
Start Date: | October 2002 |
End Date: | August 2007 |
A Phase I/II Randomized, Controlled Study of OGT 918 in Adult and Juvenile Patients With Niemann Pick C Disease
This study is done in conjunction with a trial, conducted at Columbia University College of
Physicians and Surgeons in New York and the Royal Manchester Children's Hospital in England,
to examine the effectiveness of a new drug called OGT 918 for treating Niemann-Pick Type C
(NPC) disease. Patients with this genetic disorder do not transport lipids (fatty
substances) in their cells, resulting in problems of the liver, spleen and brain. An early
sign of NPC is a reduced ability to move the eyes rapidly up and down or from side to side.
These voluntary eye movements are called saccades. Patients in the OGT 918 trial who
participate in this sub-study will have their saccadic eye movements measured to see if
improvement occurs with OGT 918 treatment.
Patients with Niemann-Pick Type C disease 12 years of age and older who are enrolled in the
OGT 918 trial described above may be eligible for this study.
Participants will have both vertical (up and down) and horizontal (side to side) saccadic
eye movements measured at two time points before starting treatment with OGT 918 and after
12 months of treatment. For the test, patients sit in a chair with their head positioned as
for a regular eye examination (steadied by a chin cup and headrest) and follow with their
eyes a series of lights or laser spots moving on a screen at a distance of 1 meter (3 feet).
During the test, patients wear either special recording glasses, infrared goggles, or
special contact lenses for measuring eye movements. A full eye evaluation lasts about 1
hour, and each eye is evaluated twice. The evaluations are separated in time by at least an
hour, and possibly a day.
Physicians and Surgeons in New York and the Royal Manchester Children's Hospital in England,
to examine the effectiveness of a new drug called OGT 918 for treating Niemann-Pick Type C
(NPC) disease. Patients with this genetic disorder do not transport lipids (fatty
substances) in their cells, resulting in problems of the liver, spleen and brain. An early
sign of NPC is a reduced ability to move the eyes rapidly up and down or from side to side.
These voluntary eye movements are called saccades. Patients in the OGT 918 trial who
participate in this sub-study will have their saccadic eye movements measured to see if
improvement occurs with OGT 918 treatment.
Patients with Niemann-Pick Type C disease 12 years of age and older who are enrolled in the
OGT 918 trial described above may be eligible for this study.
Participants will have both vertical (up and down) and horizontal (side to side) saccadic
eye movements measured at two time points before starting treatment with OGT 918 and after
12 months of treatment. For the test, patients sit in a chair with their head positioned as
for a regular eye examination (steadied by a chin cup and headrest) and follow with their
eyes a series of lights or laser spots moving on a screen at a distance of 1 meter (3 feet).
During the test, patients wear either special recording glasses, infrared goggles, or
special contact lenses for measuring eye movements. A full eye evaluation lasts about 1
hour, and each eye is evaluated twice. The evaluations are separated in time by at least an
hour, and possibly a day.
None given, verified by PI.
- INCLUSION CRITERIA:
Patients with NPC disease confirmed by abnormal cholesterol esterification and abnormal
filipin staining.
Patients aged 12 and over. Body weight must not be less than 14 kg.
Patients who can ingest a capsule.
EXCLUSION CRITERIA:
Patients younger than 18 who are unable to give informed assent and/or whose legal
guardian is unable to provide informed consent.
Patients aged 18 and over who cannot provide informed consent and/or whose legal guardian
is unable to provide witnessed informed consent.
Fertile patients who do not agree to use adequate contraception throughout the study and
for three months after cessation of OGT 918 treatment.
Patients who cannot tolerate the study procedures or who are unable to travel to the study
center as required by this protocol.
Patients currently undergoing therapy with other investigational agents or patients taking
drugs or food supplements which may interfere with gastrointestinal absorption or
motility.
Patients suffering from clinically significant diarrhoea (greater than 3 liquid stools per
day for greater than 7 days) without definable cause within 3 months of Screening Visit,
or who have a history of significant gastrointestinal disorders.
Patients with an intercurrent medical condition that would render them unsuitable for the
study e.g. HIV, hepatitis infection.
Patients who in the opinion of the investigator (for whatever reason) are thought to be
unsuitable for the study.
We found this trial at
3
sites
9000 Rockville Pike
Bethesda, Maryland 20892
Bethesda, Maryland 20892
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Columbia University In 1897, the university moved from Forty-ninth Street and Madison Avenue, where it...
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