Drug data last refreshed 20h ago · AI intelligence enriched 3w ago
ROCKLATAN is a fixed-dose combination ophthalmic solution containing netarsudil (0.02%) and latanoprost (0.005%), approved by the FDA in March 2019. It combines a Rho kinase inhibitor with a prostaglandin analog to reduce intraocular pressure in patients with open-angle glaucoma or ocular hypertension. The dual mechanism provides additive IOP-lowering effects, offering a convenient once-daily dosing option that consolidates two separate medications into a single drop.
Prostaglandin Analog
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Rocklatan Retinal Perfusion OCT Study
24-hour Effect of Rocklatan Compared With Latanoprost in Open Angle Glaucoma and Ocular Hypertension Patients
Reformulated PG324 Ophthalmic Solution for Intraocular Pressure Reduction
Improved Efficacy of Selective Laser Trabeculoplasty With the Addition of Rocklatan Post-treatment vs Artificial Tears Post-treatment
Next Generation Rocklatan
Worked on ROCKLATAN at Alcon? Share your interview experience or compensation data (+7 days Pro)
The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.
$146M Medicare spend — this is a commercially significant brand
ROCKLATAN supports roles including brand managers, medical science liaisons, field sales representatives, and commercial operations professionals focused on the glaucoma therapeutic area. Success requires expertise in ophthalmology, glaucoma pathophysiology, payer dynamics, and managed care strategy. Currently, zero open positions are linked to this product in the available data, suggesting stable team coverage or limited active recruitment.
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