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Dilaudid (hydromorphone)

University of Nebraska · FDA-approved active Small molecule

Hydromorphone is a mu-opioid receptor agonist that binds to opioid receptors in the central nervous system to produce analgesia and sedation.

Hydromorphone is a mu-opioid receptor agonist that binds to opioid receptors in the central nervous system to produce analgesia and sedation. Used for Moderate to severe pain, Severe cancer pain, Postoperative pain.

At a glance

Generic nameDilaudid (hydromorphone)
Also known asDilaudid
SponsorUniversity of Nebraska
Drug classOpioid analgesic
TargetMu-opioid receptor (μ-OR)
ModalitySmall molecule
Therapeutic areaPain Management
PhaseFDA-approved

Mechanism of action

Hydromorphone activates mu-opioid receptors throughout the brain and spinal cord, inhibiting pain signal transmission and modulating pain perception. This results in potent analgesia and is approximately 6-8 times more potent than morphine. The drug also produces sedation, euphoria, and respiratory depression through activation of opioid receptors in various CNS regions.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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