brimonidine
brimonidine: developed by 1 company · 1 clinical trial tracked · 1 FDA decision.
brimonidine evidence translation
What we can confirm
1 FDA record · 1 tracked trial
What it means
What to watch
Prepared research question
How could brimonidine → RDY affect its developer, and what evidence supports the link?
Traceable citations · Unknowns marked
See linked entities and source evidence2 indications · 1 study sponsors
Related indications
Study sponsors
Development Pipeline (1)
| Company | Phase |
|---|---|
| DR REDDYS LABORATORIES LTD (RDY) | Approved |
Clinical Trials (1)
A Multi-Center, Double-Masked Phase 3 Evaluation of the Safety and Efficacy of LNZ101 for the Treatment of Presbyopia
Primary endpoint: Percentage of Participants With a ≥ 3-line Improvement in Near Vision and no Loss ≥ 5 Letters Distance Vision
FDA Decisions1 records
Frequently asked questions
Who is developing brimonidine?
brimonidine is being developed by DR REDDYS LABORATORIES LTD.
How many clinical trials involve brimonidine?
BioSniper tracks 1 clinical trial involving brimonidine.
What is brimonidine's latest FDA decision?
The most recent tracked FDA decision for brimonidine is Approval for 1 INDICATIONS AND USAGE Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution, 0.2%/0.5% is indicated for the reduction of elevated intraocular pressure (IOP) in patients with glaucoma or ocular hypertension who require adjunctive or replacement therapy due to inadequately controlled IOP. The IOP-lowering of brimonidine tartrate/timolol maleate ophthalmic solution dosed twice a day was slightly less than that seen with the concomitant administration of 0.5% timolol maleate ophthalmic solution, dated February 16, 2024.