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Active Org.- |
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Active Indication- |
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Drug Highest PhaseDiscontinued |
First Approval Ctry. / Loc.- |
First Approval Date20 Jan 1800 |
A Multi-Center, Randomized, Double-Masked Evaluation of the Efficacy of Co-Administration of FOV1101-00 (Cyclosporine 0.01% or 0.02%) and Prednisolone Acetate 0.12% (PredMild®) Compared to Prednisolone Acetate 1% Alone or Vehicle Alone in Patients With Mild Ongoing Ocular Allergic Inflammation
This is a phase 2 study that will consist of 3 visits during a 3 week period conducted at up to 5 sites. The purpose of this study is to determine how effective the combination of Pred Mild® and FOV1101-00 is compared to either Pred Forte® alone or to vehicle alone in the prevention of eye allergies. Study subjects will be randomized to one of the following:
FOV1101-00 concentration 1 and Pred Mild®
FOV1101-00 concentration 2 and Pred Mild®
Vehicle of FOV1101-00 and Pred Forte®
Vehicle of FOV1101-00 and Vehicle of FOV1101-00
100 Clinical Results associated with CaN x PPIB x GR
100 Translational Medicine associated with CaN x PPIB x GR
0 Patents (Medical) associated with CaN x PPIB x GR