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Sinemet Cr (CARBIDOPA)

Aton · FDA-approved approved Small molecule Quality 54/100

Levodopa crosses the blood-brain barrier and is converted to dopamine in the brain, relieving Parkinson's disease symptoms.

Sinemet Cr (Carbidopa) is a small molecule aromatic amino acid decarboxylation inhibitor originally developed by Merck Sharp Dohme and currently owned by Aton. It targets lysine-specific demethylase 4E and is FDA-approved since 1975 for the treatment of Parkinson's disease, Parkinsonism, and Postencephalitic parkinsonism. As an off-patent medication, Sinemet Cr is available from multiple generic manufacturers. Key safety considerations include the potential for adverse effects such as nausea, dizziness, and orthostatic hypotension. Commercially, Sinemet Cr is widely available in the market.

At a glance

Generic nameCARBIDOPA
SponsorAton
Drug classAromatic Amino Acid [EPC]
TargetLysine-specific demethylase 4E
ModalitySmall molecule
Therapeutic areaMetabolic
PhaseFDA-approved
First approval1975

Mechanism of action

Parkinson’s disease symptoms are caused by a lack of dopamine in the brain. Levodopa, which can cross the blood-brain barrier, is converted to dopamine in the brain, thereby alleviating these symptoms.

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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