CompletedPHASE2, PHASE3NCT00328653
Efficacy and Tolerance of Nova22007 Versus Vehicle in Patients With Vernal Keratoconjunctivitis (VKC)
Studying Vernal keratoconjunctivitis
Last synced from ClinicalTrials.gov
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Report missing dataKey facts
- Sponsor
- Santen SAS
- Principal Investigator
- David BenEzra, PfHaddassah University Hospital
- Intervention
- Cyclosporine NOVA22007 0.05%(drug)
- Enrollment
- 118 target
- Eligibility
- 4 years · All sexes
- Timeline
- 2006
Study locations (1)
- Groupe Hospitalier Bichat-Claude Bernard, Paris, France
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
Open NCT00328653 on ClinicalTrials.govOther trials for Vernal keratoconjunctivitis
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