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Keveyis (DICHLORPHENAMIDE)

Xeris · FDA-approved approved Small molecule Quality 60/100

Keveyis works by inhibiting the enzyme carbonic anhydrase, which is involved in the production of aqueous humor in the eye.

Keveyis (Dichlorphenamide) is a small molecule carbonic anhydrase inhibitor developed by an unspecified original developer and currently owned by Xeris. It targets carbonic anhydrase 1 to treat various forms of glaucoma, including angle-closure, open-angle, and secondary glaucoma. Approved by the FDA in 1958, Keveyis is an off-patent medication with multiple generic manufacturers. As a carbonic anhydrase inhibitor, it works by reducing the production of aqueous humor in the eye, thereby lowering intraocular pressure. Keveyis is a valuable treatment option for patients with glaucoma, but its commercial status and pharmacokinetic properties are not well-documented.

At a glance

Generic nameDICHLORPHENAMIDE
SponsorXeris
Drug classCarbonic Anhydrase Inhibitor [EPC]
TargetCarbonic anhydrase 1
ModalitySmall molecule
Therapeutic areaOphthalmology
PhaseFDA-approved
First approval1958

Mechanism of action

Dichlorphenamide is carbonic anhydrase inhibitor. However, the precise mechanism by which dichlorphenamide exerts its therapeutic effects in patients with primary periodic paralysis is unknown.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
FDA labelMechanism, indications, dosing, boxed warnings, drug interactions
ClinicalTrials.govTrial enrolment, design, endpoints, results