Introduction: A non-interventional, multicenter, European, prospective evaluation of the effectiveness, tolerability, and safety of a topical preservative-free tafluprost (0.0015%) and timolol (0.5%) fixed-dose combination (PF tafluprost/timolol FC) in adults with open-angle glaucoma (OAG) and ocular hypertension (OHT) demonstrating insufficient response to topical beta-receptor blockers or prostaglandin analogue (PGA) monotherapy. Methods: Mean intraocular pressure (IOP) change from baseline was measured at study visits following a switch to PF tafluprost/timolol FC. Primary endpoint was absolute mean IOP change at month 6. Change from baseline concerning ocular signs and symptoms was also explored. Results: Analyses included 577 pati...
Purpose:To investigate and compare the efficacy and safety of the fixed combinations of bimatoprost ...
Objectives: The aim of this study was to evaluate the safety of preservative-free tafluprost in newl...
Objectives: The aim of this study was to evaluate the safety of preservative-free tafluprost in newl...
Introduction: A non-interventional, multicenter, European, prospective evaluation of the effectivene...
Introduction: A non-interventional, multicenter, European, prospective evaluation of the effectivene...
Purpose: Data are presented from ophthalmology clinics in Spain participating in the VISIONARY study...
Purpose: Data are presented from ophthalmology clinics in Spain participating in the VISIONARY study...
Introduction: The VISIONARY study examined the intraocular pressure (IOP)-lowering efficacy and tole...
Funding Information: Funding was provided by Santen SA for the study, medical writing services and R...
Funding Information: Funding was provided by Santen SA for the study, medical writing services and R...
Funding Information: Funding was provided by Santen SA for the study, medical writing services and R...
Purpose: Increased intraocular pressure (IOP) is the most important modifiable risk factor for the d...
The efficacy, safety and tolerability of the preservative-free (PF) fixed combination (FC) of taflup...
Ines Lanzl,1 Thomas Hamacher,2 Klaus Rosbach,3 Mohammed Osman Ramez,4 Robert Rothe,5 Eva Ružickov&aa...
Purpose: To compare the efficacy and the tolerability of preservative-free Tafluprost 0.0015% (TP) v...
Purpose:To investigate and compare the efficacy and safety of the fixed combinations of bimatoprost ...
Objectives: The aim of this study was to evaluate the safety of preservative-free tafluprost in newl...
Objectives: The aim of this study was to evaluate the safety of preservative-free tafluprost in newl...
Introduction: A non-interventional, multicenter, European, prospective evaluation of the effectivene...
Introduction: A non-interventional, multicenter, European, prospective evaluation of the effectivene...
Purpose: Data are presented from ophthalmology clinics in Spain participating in the VISIONARY study...
Purpose: Data are presented from ophthalmology clinics in Spain participating in the VISIONARY study...
Introduction: The VISIONARY study examined the intraocular pressure (IOP)-lowering efficacy and tole...
Funding Information: Funding was provided by Santen SA for the study, medical writing services and R...
Funding Information: Funding was provided by Santen SA for the study, medical writing services and R...
Funding Information: Funding was provided by Santen SA for the study, medical writing services and R...
Purpose: Increased intraocular pressure (IOP) is the most important modifiable risk factor for the d...
The efficacy, safety and tolerability of the preservative-free (PF) fixed combination (FC) of taflup...
Ines Lanzl,1 Thomas Hamacher,2 Klaus Rosbach,3 Mohammed Osman Ramez,4 Robert Rothe,5 Eva Ružickov&aa...
Purpose: To compare the efficacy and the tolerability of preservative-free Tafluprost 0.0015% (TP) v...
Purpose:To investigate and compare the efficacy and safety of the fixed combinations of bimatoprost ...
Objectives: The aim of this study was to evaluate the safety of preservative-free tafluprost in newl...
Objectives: The aim of this study was to evaluate the safety of preservative-free tafluprost in newl...