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

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
Comparator or background therapy2 trials
Phase 3 NCT03235232 Comparator Feb 2021 → Jul 2023 ocular hypertension, open-angle glaucoma EMS Completed No outcome recorded
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

NCT02718547 ↗

NCT00442312 ↗

NCT02167035 ↗

NCT03235232 ↗

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