Bimatoprost 0.01% ophthalmic solution
Sponsors
Allergan, Alcon Research
Conditions
GlaucomaGlaucoma, Open-AngleOcular HypertensionOpen-Angle Glaucoma
Phase 2
Safety and Efficacy Study of Different Formulations of Bimatoprost Once-Daily in Patients With Glaucoma or Ocular Hypertension
CompletedNCT00652496
Start: 2005-01-31End: 2005-05-31Updated: 2008-04-03
Safety and Efficacy Study of Bimatoprost in Ethnically Japanese Patients With Open-Angle Glaucoma or Ocular Hypertension
CompletedNCT00651859
Start: 2002-11-30End: 2004-01-31Updated: 2008-04-03
Phase 4
Long-Term Safety of Bimatoprost Ophthalmic Solution in Patients With Glaucoma or Ocular Hypertension
CompletedNCT01298700
Start: 2011-05-31End: 2016-12-06Updated: 2018-09-17
Assessment of Intraocular Pressure (IOP) Control in Subjects With Open-Angle Glaucoma or Ocular Hypertension Treated With Travoprost 0.004% (TRAVATAN® Z) or Bimatoprost 0.01% (LUMIGAN®)
CompletedNCT01464424
Start: 2011-10-31End: 2012-06-30Updated: 2013-09-13
An Efficacy and Tolerability Study of TRAVATAN® Versus LUMIGAN®
CompletedNCT01664039
Start: 2012-09-30End: 2014-06-30Updated: 2015-08-03
Unknown Phase
Observational Study of Lumigan® 0.01% Treatment for Patients With Primary Open Angle Glaucoma or Ocular Hypertension
CompletedNCT01489670
Start: 2011-09-30End: 2013-03-31Updated: 2014-03-28
Observational Study of Lumigan® 0.01% for Treatment of Primary Open Angle Glaucoma (POAG) or Ocular Hypertension (OHT)
CompletedNCT01568008
Start: 2011-10-31End: 2012-09-30Updated: 2013-09-20
A Study of Lumigan® 0.01% in Patients With Primary Open Angle Glaucoma (POAG) or Ocular Hypertension (OHT)
CompletedNCT01589510
Start: 2012-04-30End: 2013-02-28Updated: 2014-06-13