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Immediate Release Sublingual Buprenorphine

Royal Victoria Hospital, Canada · FDA-approved active Small molecule

Buprenorphine is a partial mu-opioid receptor agonist that binds with high affinity to reduce opioid cravings and withdrawal symptoms while producing a ceiling effect on respiratory depression.

Buprenorphine is a partial mu-opioid receptor agonist that binds with high affinity to reduce opioid cravings and withdrawal symptoms while producing a ceiling effect on respiratory depression. Used for Opioid use disorder maintenance treatment, Acute pain management, Opioid withdrawal.

At a glance

Generic nameImmediate Release Sublingual Buprenorphine
Also known asSuboxone
SponsorRoyal Victoria Hospital, Canada
Drug classPartial mu-opioid receptor agonist
TargetMu-opioid receptor (μ-OR)
ModalitySmall molecule
Therapeutic areaAddiction Medicine / Pain Management
PhaseFDA-approved

Mechanism of action

Buprenorphine acts as a partial agonist at the mu-opioid receptor, meaning it produces submaximal effects compared to full agonists like morphine. The sublingual immediate-release formulation allows rapid absorption through oral mucosa, providing faster onset of action. The partial agonist profile creates a safety ceiling for respiratory depression, making it suitable for opioid use disorder treatment with lower overdose risk than full opioids.

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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