Drug data last refreshed 20h ago · AI intelligence enriched 2w ago
BETIMOL (timolol) is a non-selective beta-adrenergic receptor antagonist ophthalmic solution approved in 1995 for reducing intraocular pressure in open-angle glaucoma, ocular hypertension, normal tension glaucoma, and ocular surface disease. Administered as eye drops, timolol works by decreasing aqueous humor production to lower IOP and reduce the risk of optic nerve damage.
BETIMOL faces imminent loss of exclusivity with modest Part D spending ($3M) and declining market relevance; team focus likely shifting to lifecycle management and transition planning.
Mechanism of action data is being enriched from DailyMed and FDA sources. Check back soon for updated drug intelligence.
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Phase 2 Study of BL1107 Eye Drops vs. Timolol in Adults With Primary Open Angle Glaucoma or Ocular Hypertension
Preservative-free Fixed-dose Combination of Tafluprost 0.0015% / Timolol 0.5% in Patients With Open-angle Glaucoma or Ocular Hypertension: Clinical Effectiveness, Tolerability and Safety in a Real World Setting
Study to Evaluate QLS-101 Compared to Timolol Maleate Eye Drops in Subjects With High Eye Pressure (Glaucoma or Ocular Hypertension).
Multicenter Study Assessing the Efficacy and Safety of DE-126 Ophthalmic Solution 0.002% Compared With Timolol Maleate Ophthalmic Solution 0.5% in Subjects With Primary Open Angle Glaucoma or Ocular Hypertension
Study Comparing the Effects of Latanoprostene Bunod and Timolol on Retinal Blood Vessel Density and Visual Acuity
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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/moBETIMOL carries minimal active recruitment signal, reflecting its mature LOE-approaching status and low Part D spending footprint ($3M). Roles tied to this product are primarily legacy commercial, patient support, and compliance-focused rather than growth-oriented.