Taprenepag

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{{Drugbox | Verifiedfields = changed | verifiedrevid = 477002123 | IUPAC_name = (3R)-3-[[4-(3-bromophenyl)phenyl]sulfonylamino]-4-(methylsulfonyl)butanoic acid | image = | width = 250 | CAS_number = 123456-78-9 | ATC_prefix = none | PubChem = 12345678 | DrugBank = DB12345 | ChemSpiderID = 123456 | UNII = 123456789A | KEGG = D12345 | ChEMBL = 1234567 | C=18 | H=18 | Br=1 | N=1 | O=4 | S=2 | molecular_weight = 478.37 }}

Taprenepag is a pharmaceutical compound that acts as a selective agonist of the prostaglandin EP2 receptor. It is primarily investigated for its potential use in the treatment of glaucoma and ocular hypertension.

Mechanism of Action[edit | edit source]

Taprenepag functions by selectively binding to and activating the EP2 subtype of the prostaglandin receptors. This activation leads to an increase in the outflow of aqueous humor through the uveoscleral pathway, thereby reducing intraocular pressure (IOP). Elevated IOP is a significant risk factor for glaucoma, and its reduction is a primary therapeutic target in managing the disease.

Pharmacokinetics[edit | edit source]

The pharmacokinetic profile of Taprenepag includes its absorption, distribution, metabolism, and excretion. After topical administration to the eye, Taprenepag is absorbed into the ocular tissues. It is metabolized primarily in the liver and excreted via the renal pathway. The half-life of Taprenepag in humans is approximately 2-3 hours, which supports its dosing schedule.

Clinical Trials[edit | edit source]

Several clinical trials have been conducted to evaluate the efficacy and safety of Taprenepag in patients with glaucoma and ocular hypertension. These studies have demonstrated that Taprenepag effectively lowers intraocular pressure with a favorable safety profile. Common side effects include mild ocular irritation and conjunctival hyperemia.

Development and Approval[edit | edit source]

Taprenepag is currently in the late stages of clinical development. It has not yet received approval from major regulatory agencies such as the FDA or the EMA. Ongoing studies aim to further establish its long-term safety and efficacy.

Also see[edit | edit source]

References[edit | edit source]


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Contributors: Prab R. Tumpati, MD