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Aldomet (METHYLDOPA)

Merck · FDA-approved approved Small molecule Quality 55/100

Aldomet (METHYLDOPA) is a small molecule drug developed by Merck, targeting Lysine-specific demethylase 4E. It belongs to the methyldopa class and was FDA-approved in 1962 for the treatment of hypertensive disorders. As an off-patent medication, Aldomet is available from multiple generic manufacturers. Key safety considerations include its potential for side effects such as drowsiness and liver damage. Aldomet has a half-life of 5.9 hours and bioavailability of 42%.

At a glance

Generic nameMETHYLDOPA
SponsorMerck
Drug classmethyldopa
TargetLysine-specific demethylase 4E
ModalitySmall molecule
Therapeutic areaNeuroscience
PhaseFDA-approved
First approval1962

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

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