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5 Not yet recruiting A Study Evaluating the Long-Term Safety of Latanoprostene Bunod Ophthalmic Solution 0.024%, in Japanese Subjects With Open-Angle Glaucoma or Ocular Hypertension
Conditions: Glaucoma; Ocular Hypertension
Intervention: Drug: Latanoprostene bunod
This study is not yet open for participant recruitment.
Verified July 2013 by Bausch & Lomb Incorporated
Sponsor:
Bausch & Lomb Incorporated
Information provided by (Responsible Party):
Bausch & Lomb Incorporated
ClinicalTrials.gov Identifier:
NCT01895972
First received: July 3, 2013
Last updated: July 8, 2013
Last verified: July 2013
History of Changes
Estimated Enrollment: 130
Study Start Date: July 2013
Estimated Study Completion Date: November 2013
Estimated Primary Completion Date: October 2013 (Final data collection date for primary outcome measure)
6 Not yet recruiting Efficacy of Latanoprostene Bunod in Lowering Intraocular Pressure in Japanese Healthy Male Volunteers
Condition: Intraocular Pressure
Intervention: Drug: Latanoprostene bunod
This study is not yet open for participant recruitment.
Verified July 2013 by Bausch & Lomb Incorporated
Sponsor:
Bausch & Lomb Incorporated
Information provided by (Responsible Party):
Bausch & Lomb Incorporated
ClinicalTrials.gov Identifier:
NCT01895985
First received: July 3, 2013
Last updated: July 10, 2013
Last verified: July 2013
History of Changes
Estimated Enrollment: 24
Study Start Date: July 2013
Estimated Study Completion Date: September 2013
Estimated Primary Completion Date: August 2013 (Final data collection date for primary outcome measure
Conditions: Glaucoma; Ocular Hypertension
Intervention: Drug: Latanoprostene bunod
This study is not yet open for participant recruitment.
Verified July 2013 by Bausch & Lomb Incorporated
Sponsor:
Bausch & Lomb Incorporated
Information provided by (Responsible Party):
Bausch & Lomb Incorporated
ClinicalTrials.gov Identifier:
NCT01895972
First received: July 3, 2013
Last updated: July 8, 2013
Last verified: July 2013
History of Changes
Estimated Enrollment: 130
Study Start Date: July 2013
Estimated Study Completion Date: November 2013
Estimated Primary Completion Date: October 2013 (Final data collection date for primary outcome measure)
6 Not yet recruiting Efficacy of Latanoprostene Bunod in Lowering Intraocular Pressure in Japanese Healthy Male Volunteers
Condition: Intraocular Pressure
Intervention: Drug: Latanoprostene bunod
This study is not yet open for participant recruitment.
Verified July 2013 by Bausch & Lomb Incorporated
Sponsor:
Bausch & Lomb Incorporated
Information provided by (Responsible Party):
Bausch & Lomb Incorporated
ClinicalTrials.gov Identifier:
NCT01895985
First received: July 3, 2013
Last updated: July 10, 2013
Last verified: July 2013
History of Changes
Estimated Enrollment: 24
Study Start Date: July 2013
Estimated Study Completion Date: September 2013
Estimated Primary Completion Date: August 2013 (Final data collection date for primary outcome measure
Ultima modifica: