Mapracorat Ophthalmic Formulation in Subjects With Allergic Conjunctivitis

Completed · Phase 2

Conditions studied: Conjunctivitis, Allergic

In brief

The objective of this study is to evaluate the dose response, and efficacy of Mapracorat ophthalmic formulation compared to its vehicle for the prevention of symptoms and signs associated with allergic conjunctivitis using a conjunctival allergen challenge (CAC) model.

Key facts

Study ID

NCT01289431

Run by

Bausch & Lomb Incorporated

People needed

236

Starts

2011-02-01

Expected to finish

2011-04-01

Last updated by the study team

2020-09-04

Who can join

Age: 12 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• positive history of ocular allergies and a positive skin test reaction
• positive bilateral CAC reaction

You may not qualify if…

• have known contraindications or sensitivities to the use of any of the study medications(s) or their components.
• have any ocular condition or significant illness that, in the opinion of the investigator, could affect the subject's safety or trial parameters.
• had ocular surgical intervention within three (3) months prior to Visit 1 or during the study and/or a history of refractive surgery within the past 3 months;
• a known history of retinal detachment, diabetic retinopathy, or active retinal disease;
• the presence of an active ocular infection or positive history of an ocular herpetic infection at any visit.
• use of any disallowed medications during the period indicated prior to Visit 1 and during the study.
• have planned surgery during the trial period or within 30 days after.
• have an intraocular pressure that is less than 5 mmHg or greater than 22 mmHg or any type of glaucoma at Visit 1

Where it is running

• Bausch & Lomb — Rochester, New York, United States

Full record on ClinicalTrials.gov

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