Drugs / Combigan

Regulatory milestones approvals, filings & regulatory actions · 1 recorded

MilestoneJurisdictionBrandIndicationDateSentence it was read from
Approved US (FDA) COMBIGAN 2007-10-30 fda.gov

Trials 3 · a red edge is where a trial was stopped

2006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 41 trial
Phase 4 NCT00442312 May → Nov 2006 glaucoma Genovate Biotechnology Co., Ltd. Unknown No outcome recorded
Phase not applicable2 trials
NCT04296916 Apr 2020 → Oct 2024 borderline glaucoma, myopia Sun Yat-sen University Unknown No outcome recorded
NCT02718547 Mar 2017 → Mar 2018 diabetic retinopathy Meir Medical Center Unknown No outcome recorded
Also used as a comparator or background therapy in 2 trials
PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 31 trial
Phase 3 NCT03235232 Comparator Feb 2021 → Jul 2023 ocular hypertension, open-angle glaucoma EMS Completed No outcome recorded
Phase 41 trial
Phase 4 NCT02167035 Comparator Aug 2014 → Mar 2018 glaucoma, ocular hypertension Cornerstone Health Care, PA Completed No outcome recorded

Evidence & citations 2 cited values

Every value below carries the sentence it was read from. 5 sources stand behind the page.

FieldValueCited text
Known as Combigan “If necessary, latanoprost and timolol will be switched to Xalacom eye drops, timolol and alphagan will be switched to Combigan eye drops, timolol and brinzolamide will be...” NCT04296916
4

NCT03235232

NCT00442312

NCT02718547

NCT02167035

Route Topical “1 drop of Combigan® in the affected eye(s), twice a day (approximately each 12 hours) for 8 weeks.” NCT03235232