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Akineton (BIPERIDEN)

AbbVie · FDA-approved approved Small molecule Quality 40/100

Akineton (Biperiden) is a small molecule anticholinergic medication originally developed by AbbVie and currently owned by the same company. It targets the muscarinic acetylcholine receptor M1 and is used to treat various conditions related to Parkinson's disease, including arteriosclerotic parkinsonism, extrapyramidal disease, and postencephalitic parkinsonism. Akineton was first approved by the FDA in 1959 and remains off-patent, with no active Orange Book patents. It has a half-life of 24 hours and bioavailability of 30%. As an anticholinergic, Akineton can have significant side effects, particularly in older adults, and its use should be carefully monitored.

At a glance

Generic nameBIPERIDEN
SponsorAbbVie
Drug classAnticholinergic
TargetMuscarinic acetylcholine receptor M1
ModalitySmall molecule
Therapeutic areaNeuroscience
PhaseFDA-approved
First approval1959

Approved indications

Common side effects

No common side effects on file.

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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