Clinical trial

Efficacy and Tolerance of Nova22007 Versus Vehicle in Patients With Vernal…

NCT00328653 · Santen SAS, Industry · Completed

Key facts

NCT number NCT00328653
Title Efficacy and Tolerance of Nova22007 Versus Vehicle in Patients With Vernal Keratoconjunctivitis (VKC)
Official title Phase II/III, Multicenter, Double-Masked, Randomized, Parallel Group, Dose Ranging, Controlled Trial of Efficacy and Tolerance of Nova22007 (Cyclosporine A [CSA] 0.05% & 0.1% Ophthalmic Cationic Emulsion) Versus Vehicle in Patients With VKC
Lead sponsor Santen SAS, Industry
Status Completed
Phase Phase 2/Phase 3
Study type Interventional
Conditions Conjunctivitis, Vernal
Intervention type Drug
Interventions Cyclosporine NOVA22007 0.05%, Cyclosporine NOVA22007 0.1%, Vehicle
Enrollment 118
Start date May 1, 2006
Primary completion Feb 22, 2007
First posted May 22, 2006
Last update posted Dec 14, 2021
Countries France

At a glance

  • 1–9 Study sites
  • Yes Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About ClinicalTrials.gov studies

ClinicalTrials.gov is the U.S. National Library of Medicine's registry of clinical studies conducted around the world. Contact and investigator details are not shown here.

Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

Browse all ClinicalTrials.gov studies