Last reviewed · How we verify

double dose Morphine

Norwegian University of Science and Technology · Phase 3 active Small molecule

Morphine acts as a mu-opioid receptor agonist, producing analgesia by activating these receptors in the brain and spinal cord.

Morphine acts as a mu-opioid receptor agonist, producing analgesia by activating these receptors in the brain and spinal cord. Used for Pain management in patients with cancer, Pain management in patients with acute injuries or postoperative pain.

At a glance

Generic namedouble dose Morphine
SponsorNorwegian University of Science and Technology
Drug classopioid
Targetmu-opioid receptor
ModalitySmall molecule
Therapeutic areaPain management
PhasePhase 3

Mechanism of action

Morphine's analgesic effects are primarily mediated through its binding to mu-opioid receptors, which are G protein-coupled receptors that inhibit the release of pain-producing neurotransmitters. This results in a decrease in the perception of pain. Additionally, morphine can also produce respiratory depression and euphoria through its action on these receptors.

Approved indications

Common side effects

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

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

Competitive intelligence

For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape: