Ignite Creation Date:
2024-05-05 @ 11:21 AM
Last Modification Date:
2024-10-26 @ 9:02 AM
Study NCT ID:
NCT00001736
Status:
COMPLETED
Last Update Posted:
2008-03-04
First Post:
1999-11-03
Brief Title:
New Cysteamine Eye Drops Formulation to Treat Corneal Crystals in Cystinosis
Sponsor:
National Eye Institute NEI
Organization:
National Institutes of Health Clinical Center CC
Study Overview
Official Title:
Safety and Efficacy Trial of a Proposed NDA Formulation of Topical Cysteamine in the Treatment of Corneal Cystine Crystal Accumulation in Cystinosis
Status:
COMPLETED
Status Verified Date:
2000-04
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
This study will evaluate the safety and effectiveness of a new formulation of eye drops used to treat cystine crystals that form in the corneas of patients with cystinosis Cystinosis is an inherited disease caused by a defective enzyme in which excessive amounts of the amino acid cystine accumulate in the body Among others symptoms include poor growth and development of kidney failure In addition after 10 to 20 years the cornea-the outside covering of the eye over the iris and pupils-becomes so packed with cystine crystals that small painful breaks may develop
This corneal condition is treated with cysteamine eye drops This study is designed to provide additional information about this medication that the Food and Drug Administration requires before approving it for marketing The study will examine in two separate but simultaneous investigations the safety and effectiveness of a new cysteamine formulation In both studies before treatment begins patients will have a complete eye examination and photographs of the eye will be taken using a bright flash
Safety Study
Children and adults currently enrolled in a cystinosis study at the National Institutes of Health may participate in this trial They will receive the current cysteamine formulation in one eye and the new preparation in the other eye The drops will be given every hour during waking hours Patients will be observed daily for the first week of treatment and will be called at 2 weeks and 4 weeks to check on side effects if any At 6 months they will undergo a repeat eye examination Patients or their parents will keep a daily diary recording the condition of each eye
Effectiveness Study
Children and adults from Ann Arbor Michigan LaJolla California and the NEI clinic may be enrolled in this study Participants will receive medication as described above for the safety trial They will be observed daily for the first week and will have repeat eye examinations including photographs at months 3 6 9 and 12 to see if the crystals have decreased Patients will keep a daily diary of the condition of both eyes
This corneal condition is treated with cysteamine eye drops This study is designed to provide additional information about this medication that the Food and Drug Administration requires before approving it for marketing The study will examine in two separate but simultaneous investigations the safety and effectiveness of a new cysteamine formulation In both studies before treatment begins patients will have a complete eye examination and photographs of the eye will be taken using a bright flash
Safety Study
Children and adults currently enrolled in a cystinosis study at the National Institutes of Health may participate in this trial They will receive the current cysteamine formulation in one eye and the new preparation in the other eye The drops will be given every hour during waking hours Patients will be observed daily for the first week of treatment and will be called at 2 weeks and 4 weeks to check on side effects if any At 6 months they will undergo a repeat eye examination Patients or their parents will keep a daily diary recording the condition of each eye
Effectiveness Study
Children and adults from Ann Arbor Michigan LaJolla California and the NEI clinic may be enrolled in this study Participants will receive medication as described above for the safety trial They will be observed daily for the first week and will have repeat eye examinations including photographs at months 3 6 9 and 12 to see if the crystals have decreased Patients will keep a daily diary of the condition of both eyes
Detailed Description:
The primary purpose of this study is to evaluate the safety and efficacy of a new formulation of cysteamine eye drops to treat children and adults with cystinosis and cystine crystal accumulation in the cornea The safety of this new formulation will be evaluated among 30 children and adults with a history of cystinosis under treatment at the NIH with the current preparation of cysteamine eye drops Patients will be randomized to the current preparation in one eye and the new formulation in the other eye Vision blurring redness pain irritation and itching will be evaluated in each eye at Week 1 Week 2 Week 4 and Month 6 Complete ophthalmic evaluation including corneal slit lamp examination with photographs will be performed at baseline and 6 months at the NEI Clinical Center
Efficacy will be evaluated among 15 patients 5 each from the NEI Clinical Center Ann Arbor Michigan and La Jolla California who have not received cysteamine eye drops prior to enrollment Patients will be randomized to the current preparation in one eye and the new formulation in the other eye Vision blurring redness pain irritation and itching will be evaluated in each eye and a complete ophthalmic assessment including a corneal slit lamp examination with photographs will be performed at baseline Month 3 Month 6 Month 9 and Month 12 The primary efficacy outcome measure will be the improvement in the new formulation treated eye by 100 unit on a corneal photograph scale from 000 to 300 in 025 increments compared to the baseline grade This scale grades the density and number of crystals in the cornea The safety and efficacy studies will be conducted concurrently
Efficacy will be evaluated among 15 patients 5 each from the NEI Clinical Center Ann Arbor Michigan and La Jolla California who have not received cysteamine eye drops prior to enrollment Patients will be randomized to the current preparation in one eye and the new formulation in the other eye Vision blurring redness pain irritation and itching will be evaluated in each eye and a complete ophthalmic assessment including a corneal slit lamp examination with photographs will be performed at baseline Month 3 Month 6 Month 9 and Month 12 The primary efficacy outcome measure will be the improvement in the new formulation treated eye by 100 unit on a corneal photograph scale from 000 to 300 in 025 increments compared to the baseline grade This scale grades the density and number of crystals in the cornea The safety and efficacy studies will be conducted concurrently
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None
Secondary IDs
| Secondary ID | Type | Domain | Link |
|---|---|---|---|
| 98-EI-0109 | None | None | None |