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Lusedra (FOSPROPOFOL)

FDA-approved approved Small molecule Quality 24/100

Lusedra (FOSPROPOFOL) is a small molecule drug that targets the GABA-A receptor, classified as a fospropofol. It was originally developed and is currently owned by a pharmaceutical company. Lusedra is FDA-approved for sedation as an adjunct to anesthesia and was approved in 2008. It is off-patent, meaning there are no active Orange Book patents, and there are no generic manufacturers. As an off-patent drug, its commercial status is subject to change.

At a glance

Generic nameFOSPROPOFOL
Drug classfospropofol
TargetGABA-A receptor
ModalitySmall molecule
Therapeutic areaNeuroscience
PhaseFDA-approved
First approval2008

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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