Indivior Announces the Publication of New Data on the Comparative Effectiveness of Intranasal (IN) Nalmefene (OPVEE 2.7mg) and IN Naloxone (4 mg) in a Translational Model Assessing the Impact of a Synthetic Opioid Overdose on Respiratory Depression and Cardiac Arrest
Indivior has published new data comparing the effectiveness of intranasal (IN) nalmefene (OPVEE 2.7mg) and IN naloxone (4 mg) in reversing synthetic opioid overdoses. The study, using a validated translational model, shows that a single dose of OPVEE significantly reduces simulated cardiac arrests caused by fentanyl and carfentanil overdoses compared to naloxone. For instance, a single OPVEE dose reduced the cardiac arrest rate to 12% in chronic opioid users, whereas naloxone reduced it to 47%. Multiple naloxone doses were required to match OPVEE's effectiveness. The simulation involved 2000 virtual patients, highlighting OPVEE's superior performance in reversing overdoses, which is critical given the high rates of synthetic opioid-linked fatalities in the US. These findings could inform better emergency response strategies.
- Single dose of OPVEE (2.7mg) significantly reduces incidence of simulated cardiac arrest in fentanyl and carfentanil overdoses.
- In chronic opioid users, OPVEE reduced cardiac arrest rate to 12% compared to 47% with single-dose naloxone.
- Simulations involved 2000 virtual patients, showing robust data support.
- Findings could enhance emergency response strategies for synthetic opioid overdoses.
- Study based on simulated data, not real-world clinical trials.
- OPVEE outperformed naloxone, potentially indicating higher costs for effective overdose reversal.
Insights
This publication highlights significant advancements in the treatment of synthetic opioid overdoses, particularly with the use of IN OPVEE (nalmefene) compared to IN naloxone. The study shows that nalmefene is considerably more effective in reducing the incidence of cardiac arrest following a synthetic opioid overdose. OPVEE decreased cardiac arrest incidence to 12% compared to 47% with a single dose of naloxone and only high doses of naloxone could approach the effectiveness of OPVEE. This difference is crucial, especially given the rapid progression from respiratory depression to cardiac arrest in opioid overdoses.
The methodology's robustness, including simulations with 2000 virtual patients, adds credibility to these findings. This result suggests potential changes in clinical guidelines and first-responder protocols, emphasizing the need for more effective overdose-reversing agents like nalmefene.
For investors, this information underscores the clinical value and market potential of OPVEE. With synthetic opioid overdoses being a critical public health issue, the acceptance and adoption of nalmefene could drive significant revenue growth for Indivior. Furthermore, the publication in a peer-reviewed journal adds scientific validation, potentially accelerating regulatory approvals and market penetration.
From a market perspective, the data on OPVEE's effectiveness compared to naloxone is promising. Given the increasing number of synthetic opioid overdoses, first responders and healthcare providers are in dire need of more potent treatment options. OPVEE's superior performance in reducing cardiac arrest incidence suggests a strong competitive advantage.
For retail investors, it's important to recognize the potential market share that OPVEE could capture. Naloxone has long been the standard treatment for opioid overdoses, but its limited effectiveness against potent synthetic opioids like fentanyl and carfentanil presents a substantial opportunity for OPVEE.
Additionally, with the incidence of opioid overdoses continuing to rise, there is a growing addressable market. If OPVEE can secure regulatory approval and gain traction among healthcare providers and emergency responders, it could significantly impact Indivior's financial performance positively.
- Large reductions in the incidence of simulated cardiac arrest caused by potentially lethal doses of fentanyl or carfentanil were observed following a single IN dose of OPVEE compared to a single dose of IN naloxone.
- Across scenarios of fentanyl or carfentanil overdoses, simultaneous administration of four doses of IN naloxone (4×4 mg) was needed to reduce the incidence of simulated cardiac arrest to values approaching those obtained with a single dose of OPVEE (3mg). Modeling predictions in chronic opioid users indicate that the incidence of cardiac arrest following an intravenous (IV) fentanyl overdose (2.97 mg) decreased from
78% in the absence of intervention to12% with OPVEE and47% with a 4 mg IN dose of naloxone.
Model simulations were performed using a validated translational model1 developed by the Division of Applied Regulatory Science in the US Food and Drug Administration's Center for Drug Evaluation and Research. In the present study, this translational model was further expanded with data from pharmacokinetic and pharmacodynamic studies with OPVEE2,3 and IN naloxone pharmacokinetic data.2 Simulations were conducted in 2000 virtual patients. Following an IV dose of 2.97 mg fentanyl that resulted in a
Simulations in opioid naïve individuals illustrated the same trend, although a higher incidence of cardiac arrest was predicted in this population given the lack of tolerance to the respiratory effects of opioids. Simulation of an IV fentanyl overdose (2.97 mg) in opioid naïve individuals led to an incidence of cardiac arrest of
More than 78,200 fatal opioid overdoses in the US were reported in the one year ending December 2023, with almost
"These modeling data are relevant considering today's overdose epidemic with increasing prevalence of overdoses from illicitly manufactured synthetic opioids, which can be extremely difficult to reverse6," said Christian Heidbreder, PhD, Chief Scientific Officer, Indivior, Inc. "These simulated data serve two purposes. First, they quantify the challenge of effectively reversing a synthetic opioid overdose. Second, these data inform the approach for first responders (e.g., police, fire and rescue personnel, friends and family of the overdose victim) in a community setting that does not benefit from the ventilatory support available in an Emergency Department. Without adequate ventilatory support, there is a limited time window before hypoxic injury is irreversible and cardiac arrest occurs; this can happen extremely rapidly with fentanyl and other synthetic opioids7."
Similar effects were observed following opioid overdose simulations using carfentanil, which is 100-times more potent than fentanyl.8 These trends remain consistent for both chronic and opioid naïve individuals overdosing on carfentanil.
About OPVEE®
OPVEE (nalmefene) nasal spray
INDICATION
OPVEE nasal spray is an opioid antagonist indicated for the emergency treatment of known or suspected overdose induced by natural or synthetic opioids in adults and pediatric patients aged 12 years and older, as manifested by respiratory and/or central nervous system depression.
OPVEE nasal spray is intended for immediate administration as emergency therapy in settings where opioids may be present.
OPVEE nasal spray is not a substitute for emergency medical care.
HIGHLIGHTED SAFETY INFORMATION
CONTRAINDICATIONS
Hypersensitivity to nalmefene or to any of the other ingredients.
WARNINGS AND PRECAUTIONS
Risk of Recurrent Respiratory and Central Nervous System Depression: While the duration of action of nalmefene is as long as most opioids, a recurrence of respiratory depression is possible, therefore, keep patient under continued surveillance and administer repeat doses of OPVEE using a new nasal spray with each dose, as necessary, while awaiting emergency medical assistance.
Limited Efficacy with Partial Agonists or Mixed Agonist/Antagonists: Reversal of respiratory depression caused by partial agonists or mixed agonists/antagonists, such as buprenorphine and pentazocine, may be incomplete. Larger or repeat doses may be required.
Precipitation of Severe Opioid Withdrawal: Use in patients who are opioid dependent may precipitate opioid withdrawal. In neonates, opioid withdrawal may be life-threatening if not recognized and properly treated. Monitor for the development of opioid withdrawal.
Risk of Cardiovascular (CV) Effects: Abrupt postoperative reversal of opioid depression may result in adverse CV effects. These events have primarily occurred in patients who had preexisting CV disorders or received other drugs that may have similar adverse CV effects. Monitor these patients closely in an appropriate healthcare setting after use of nalmefene hydrochloride.
Risk of Opioid Overdose from Attempts to Overcome the Blockade: Attempts to overcome opioid withdrawal symptoms caused by opioid antagonists with high or repeated doses of exogenous opioids may lead to opioid intoxication and death.
ADVERSE REACTIONS
Most common adverse reactions (incidence at least
For more information about OPVEE and the full Prescribing Information visit www.opvee.com.
About Indivior
Indivior is a global pharmaceutical company working to help change patients' lives by developing medicines to treat substance use disorders (SUD), opioid overdose and serious mental illnesses. Our vision is that all patients around the world will have access to evidence-based treatment for the chronic conditions and co-occurring disorders of SUD. Indivior is dedicated to transforming SUD from a global human crisis to a recognized and treated chronic disease. Building on its global portfolio of opioid use disorder treatments, Indivior has a pipeline of product candidates designed to both expand on its heritage in this category and potentially address other chronic conditions and co-occurring disorders of SUD. Headquartered in
1. Mann J, Samieegohar M, Chaturbedi A, Zirkle J, Han X, Ahmadi SF, Eshleman A, Janowsky A, Wolfrum K, Swanson T, Bloom S, Dahan A, Olofsen E, Florian J, Strauss DG, Li Z. Development of a Translational Model to Assess the Impact of Opioid Overdose and Naloxone Dosing on Respiratory Depression and Cardiac Arrest. Clin Pharmacol Ther. 2022 Nov;112(5):1020-1032. doi: 10.1002/cpt.2696. Epub 2022 Jul 22. PMID: 35766413. |
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6. Karila, L., Marillier, M., Chaumette, B., Billieux, J., Franchitto, N., & Benyamina, A. (2019). New synthetic opioids: Part of a new addiction landscape. Neuroscience & Biobehavioral Reviews/Neuroscience and Biobehavioral Reviews, 106, 133–140. https://doi.org/10.1016/j.neubiorev.2018.06.010 |
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