Clinical trial

Determination Of Predictive Factors Allowing To An Additional 10% Reduction Of…

NCT00230763 · Pfizer's Upjohn has merged with Mylan to form Viatris Inc., Industry · Completed

Key facts

NCT number NCT00230763
Title Determination Of Predictive Factors Allowing To An Additional 10% Reduction Of Intra-Ocular Pressure
Official title Determination Of Predictive Factors Allowing To An Additional 10% Reduction Of Intra-Ocular Pressure After A 12-Week Treatment With Latanoprost 0.005% / Timolol 0.5% Fixed Combination (Xalacom) In Previously Treated Patients With Open Angle Glaucoma Or Ocular Hypertension
Acronym PREDICOM
Lead sponsor Pfizer's Upjohn has merged with Mylan to form Viatris Inc., Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Glaucoma, Primary Open Angle (POAG), Ocular Hypertension
Intervention type Drug, Procedure
Interventions GSS questionnaire, IOP, LATANOPROST 0.005% / TIMOLOL 0.5% FIXED COMBINATION, Visual acuity
Enrollment 396
Start date Sep 1, 2005
Primary completion Oct 1, 2007
Completion Oct 1, 2007
First posted Oct 3, 2005
Last update posted Feb 18, 2021
Countries France

At a glance

  • 100–999 Study sites
  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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