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A Study to Evaluate Efficacy and Safety Effects Using Mikelan® LA Ophthalmic Solution (OS) 2% Versus Timoptol® XE Ophthalmic Solution (OS) 0.5% in Ocular Hypertension Patients

2014-08-27 03:19:31 | BioPortfolio

Summary

The primary objective of the clinical study is to evaluate the efficacy and safety for Mikelan LA eye drops 2% (once per day) of intra-ocular pressure decreased.

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Conditions

Glaucoma

Intervention

carteolol (Mikelan), timolol (Timoptol), latanoprost (Xalatan)

Location

Tri-Service General Hospital
Taipei
Taiwan

Status

Recruiting

Source

Taiwan Otsuka Pharm. Co., Ltd

Results (where available)

View Results

Links

Published on BioPortfolio: 2014-08-27T03:19:31-0400

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