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Phase 2 N=328 Treatment

Cysteamine Eye Drops to Treat Corneal Crystals in Cystinosis

Cystinosis

Enrolled (actual)
328
Serious AEs
3.4%
Results posted
Jul 2014
Primary outcome: Primary: Number of Participants With Serious and Non-Serious Adverse Events — 257 participants

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
Cysteamine (Drug)
Age
Pediatric, Adult, Older Adult · 2+ yrs
Sex
All
Sponsor
National Eye Institute (NEI)
Primary completion
Jul 2013

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Participants With Serious and Non-Serious Adverse Events
257
PRIMARY
Number of Eyes With a Corneal Cystine Crystal Score (CCCS) Response
98

Summary

Cystinosis is an inherited disease that results in poor growth and kidney disease, among other things. The damage to the kidneys and other organs is thought to be due to accumulation of cystine inside the cells of various body tissues. This chemical also accumulates in the cornea-the covering of the eye over the pupil and iris. After 10 to 20 years, the corneas of some patients become so packed with crystals that the surfaces may become irregular, occasionally causing small, painful breaks. Patients enrolled in a NIH study on cystinosis are receiving the drug cysteamine. Taken by mouth, this drug reduces cystine in some tissues, but not in the cornea. This study began in 1986 to test whether cysteamine eye drops could prevent or reduce corneal cystine crystals in these patients. The drops have been very effective in removing crystals and reducing pain in patients who take the medication as directed. Patients who do not take the medication as prescribed do not benefit. After the effectiveness of the drops was proven, the main purpose was modified to continue to evaluate the long-term safety and effectiveness of cysteamine eye drops for treating cystine crystals in the corneas of patients with cystinosis until the drops are approved by the Food and Drug Administration (FDA). When the New Drug Application (NDA) for the Sigma-Tau standard formulation is granted, this protocol will be terminated.

Eligibility Criteria

INCLUSION CRITERIA

  • Patients must have a documented clinical diagnosis of cystinosis.
  • Patients should be 2 years old or older.

EXCLUSION CRITERIA

  • Inability to travel to NIH for a baseline examination, after 1 year, and every two years thereafter for follow-up
  • Inability to cooperate for slit-lamp examination
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00001213). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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