alitretinoin
PANRETIN (alitretinoin) is (9-cis-retinoic acid) is a naturally occurring endogenous retinoid that binds to and activates all known intracellular retinoid receptor subtypes (rarα, rarβ, rarγ, rxrα, rxrβ and rxrγ). First approved in 1999.
Drug data last refreshed 52m ago · AI intelligence enriched 1mo ago
PANRETIN (alitretinoin) is a topical retinoid gel approved in 1999 for cutaneous manifestations of Kaposi's sarcoma. It works as a 9-cis-retinoic acid that activates all known intracellular retinoid receptors (RAR and RXR subtypes), functioning as a transcription factor to regulate cellular differentiation and proliferation in neoplastic cells. The drug directly inhibits KS cell growth in vitro through this receptor-mediated mechanism.
Minimal commercial infrastructure; product serves a niche indication with low claims volume and declining lifecycle stage.
(9-cis-retinoic acid) is a naturally occurring endogenous retinoid that binds to and activates all known intracellular retinoid receptor subtypes (RARα, RARβ, RARγ, RXRα, RXRβ and RXRγ). Once activated these receptors function as transcription factors that regulate the expression of genes that…
Retinoid
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
A 24 Week Trial to Compare the Efficacy and Safety of Delgocitinib Cream 20 mg/g Twice-daily With Alitretinoin Capsules Once-daily in Adult Participants With Severe Chronic Hand Eczema
Study of Efficacy and Safety of Brolucizumab Versus Panretinal Photocoagulation Laser in Patients With Proliferative Diabetic Retinopathy
Prospective, Randomized, Multicentre, Open-label, Phase II / III Study to Assess Efficacy and Safety of Ranibizumab 0.5 mg Intravitreal Injections Plus Panretinal Photocoagulation (PRP) Versus PRP in Monotherapy in the Treatment of Subjects With High Risk Proliferative Diabetic Retinopathy.
Prompt Panretinal Photocoagulation Versus Ranibizumab+Deferred Panretinal Photocoagulation for Proliferative Diabetic Retinopathy
Efficacy and Safety of Oral Alitretinoin (Toctino®) in the Treatment of Patients With Cutaneous Lupus Erythematosus
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.
PANRETIN offers limited career growth opportunities given its niche indication, minimal claims volume ($965K Part D spending), and approaching loss of exclusivity. This role is best suited for professionals seeking specialized dermatologic oncology expertise or those willing to manage a declining product line.
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