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Sublingual Buprenorphine (SLB)

NYU Langone Health · FDA-approved active Small molecule

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

At a glance

Generic nameSublingual Buprenorphine (SLB)
SponsorNYU Langone Health
Drug classPartial mu-opioid receptor agonist
TargetMu-opioid receptor (μ-OR)
ModalitySmall molecule
Therapeutic areaAddiction Medicine / Pain Management
PhaseFDA-approved

Mechanism of action

Buprenorphine's partial agonist activity at the mu-opioid receptor produces analgesia and reduces opioid withdrawal symptoms with lower abuse potential than full agonists. The sublingual formulation allows rapid absorption through oral mucosa, bypassing first-pass metabolism. Its high receptor binding affinity and ceiling effect on respiratory depression make it safer than full opioid agonists in overdose scenarios.

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

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