CEQUA (cyclosporine) by Fosun Pharma is calcineurin inhibitors [moa]. Approved for dry eye disease, kidney transplantation, liver transplantation. First approved in 2018.
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CEQUA is a calcineurin inhibitor immunosuppressant delivered as an ophthalmic solution containing cyclosporine. Approved by the FDA in August 2018, it is indicated for the treatment of dry eye disease by reducing inflammation and suppressing immune-mediated tear gland dysfunction. The drug works by inhibiting calcineurin-dependent T-cell activation, thereby modulating the immune response in the ocular surface. CEQUA represents a branded formulation strategy in a market historically dominated by the original cyclosporine product RESTASIS.
Calcineurin Inhibitors
Calcineurin Inhibitor Immunosuppressant
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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.
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Upgrade to Pro — $25/moCEQUA's peak-stage status creates opportunities for brand management, product managers focused on market share defense, and medical science liaisons engaging ophthalmologists and retina specialists. Success in this role requires deep knowledge of dry eye disease pathophysiology, formulary placement strategy, and competitive positioning against entrenched RESTASIS dominance. Currently, zero open positions are linked to this product in the available dataset, suggesting a mature, stable team structure without active expansion.