Evidence map›Paper›PMID 39347921›Full record

Trial reportJournal of clinical pharmacology2025

Time Course of Reversal of Fentanyl-Induced Respiratory Depression in Healthy Subjects by Intramuscular Nalmefene and Intramuscular and Intranasal Naloxone.

Alessandra Cipriano, Glen Apseloff, Ram P Kapil, Ellie He, Manjunath Shet, Stephen C Harris

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of clinical pharmacology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Trial
  2. A Fentanyl-Responsive Microneedle Patch for Harm Reduction.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Alessandra CiprianoImbrium Therapeutics L.P., a subsidiary of Purdue Pharma L.P., Stamford, CT, USA.
Glen ApseloffOhio Clinical Trials, Inc., Columbus, OH, USA.
Ram P KapilImbrium Therapeutics L.P., a subsidiary of Purdue Pharma L.P., Stamford, CT, USA.
Ellie HeImbrium Therapeutics L.P., a subsidiary of Purdue Pharma L.P., Stamford, CT, USA.
Manjunath ShetImbrium Therapeutics L.P., a subsidiary of Purdue Pharma L.P., Stamford, CT, USA.
Stephen C HarrisImbrium Therapeutics L.P., a subsidiary of Purdue Pharma L.P., Stamford, CT, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The increase in opioid overdose deaths, particularly involving potent, long-acting synthetic opioids, has led to calls for stronger, longer-acting opioid-overdose-reversal agents. Using an opioid-induced respiratory depression model, we investigated the onset and time course of action of naloxone and a long-acting opioid antagonist, nalmefene, in reversing the effects of an ongoing intravenous fentanyl infusion over a period of up to 100 min. Healthy, moderately experienced opioid users received intramuscular (IM) nalmefene 1 mg, IM naloxone 2 mg, or intranasal (IN) naloxone 4 mg after fentanyl-induced respiratory depression was established based on reduction in respiratory minute volume (MV). Each participant received each opioid antagonist twice per a randomized crossover schedule. Reversal of respiratory depression, pharmacokinetics, and safety were investigated. Participants showed rapid increases in plasma opioid antagonist concentrations, and meaningful reversal of depressed MV tended to occur earlier with IM nalmefene and IM naloxone than with IN naloxone. Compared to naloxone, nalmefene provided extended exposure, and mean MV was maintained at a higher level. All participants experienced treatment-related adverse events, but none were severe, serious, or led to study drug discontinuation. This study provides evidence that IM nalmefene 1 mg achieves reversal of fentanyl-induced respiratory depression similar to or better than that achieved with standard-of-care naloxone treatments. No new safety concerns were raised for IM nalmefene at the tested dose. The pharmacokinetic and pharmacodynamic properties of IM nalmefene position it as an important treatment option in opioid overdose reversal, particularly given the increasing prevalence of overdoses involving potent, long-acting synthetic opioids.

Indexed as

Analgesics, OpioidFentanylNaloxoneNaltrexoneNarcotic AntagonistsRespiratory InsufficiencyAdministration, IntranasalAdultCross-Over StudiesFemaleHealthy VolunteersHumansInjections, IntramuscularMaleMiddle AgedYoung AdultAnalgesics, OpioidFentanylnalmefeneNaloxoneNaltrexoneNarcotic Antagonistsfentanylnalmefenenaloxoneopioid antagonistopioid overdosepharmacodynamicspharmacokineticsrespiratory depression reversal

Identifiers

PMID39347921
PMCPMC11771590

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.