Evaluation of the abuse potential of pitolisant, a selective [H.sub.3]-receptor antagonist/inverse agonist, for the treatment of adult patients with narcolepsy with or without cataplexy

Objectives: To evaluate the human abuse potential of pitolisant, a selective histamine 3 ([H.sub.3])-receptor antagonist/inverse agonist recently approved by the US Food and Drug Administration for the treatment of excessive daytime sleepiness in adult patients with narcolepsy. Methods: Nondependent...

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Veröffentlicht in:Sleep (New York, N.Y.) N.Y.), 2020-04, Vol.43 (4), p.1
Hauptverfasser: Setnik, Beatrice, McDonnell, Michael, Mills, Catherine, Scart-Gres, Catherine, Robert, Philippe, Dayno, Jeffrey M, Schwartz, Jean-Charles
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container_issue 4
container_start_page 1
container_title Sleep (New York, N.Y.)
container_volume 43
creator Setnik, Beatrice
McDonnell, Michael
Mills, Catherine
Scart-Gres, Catherine
Robert, Philippe
Dayno, Jeffrey M
Schwartz, Jean-Charles
description Objectives: To evaluate the human abuse potential of pitolisant, a selective histamine 3 ([H.sub.3])-receptor antagonist/inverse agonist recently approved by the US Food and Drug Administration for the treatment of excessive daytime sleepiness in adult patients with narcolepsy. Methods: Nondependent, recreational stimulant users able to distinguish phentermine HCl 60 mg from placebo in a drug discrimination test were randomized in a four-period, double-blind, crossover design to receive single doses of pitolisant 35.6 mg (therapeutic dose), pitolisant 213.6 mg (supratherapeutic dose), phentermine HCl 60 mg, and placebo. The primary endpoint was maximum effect ([E.sub.max]) on the 100-point Drug Liking ("at this moment") visual analog scale. Results: In 38 study completers (73.7% male; 65.8% white; mean age, 33.3 years), mean Drug Liking [E.sub.max] was significantly greater for phentermine versus pitolisant 35.6 mg (mean difference, 21.4; p < 0.0001) and pitolisant 213.6 mg (mean difference, 19.7; p < 0.0001). Drug Liking [E.sub.max] was similar for pitolisant (both doses) and placebo. Similarly, for key secondary measures of Overall Drug Liking and willingness to Take Drug Again, mean [E.sub.max] scores were significantly greater for phentermine versus pitolisant (both doses) and similar for pitolisant (both doses) versus placebo. The incidence of adverse events was 82.1% after phentermine HCl 60 mg, 72.5% after pitolisant 213.6 mg, 47.5% after pitolisant 35.6 mg, and 48.8% after placebo administration. Conclusions: In this study, pitolisant demonstrated significantly lower potential for abuse compared with phentermine and an overall profile similar to placebo; this suggests a low risk of abuse for pitolisant. Clinical Trial Registration: ClinicalTrials.gov NCT03152123. Determination of the abuse potential of pitolisant in healthy, nondependent recreational stimulant users. Key words: drug abuse; narcolepsy; pitolisant
doi_str_mv 10.1093/sleep/zsz252
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Methods: Nondependent, recreational stimulant users able to distinguish phentermine HCl 60 mg from placebo in a drug discrimination test were randomized in a four-period, double-blind, crossover design to receive single doses of pitolisant 35.6 mg (therapeutic dose), pitolisant 213.6 mg (supratherapeutic dose), phentermine HCl 60 mg, and placebo. The primary endpoint was maximum effect ([E.sub.max]) on the 100-point Drug Liking ("at this moment") visual analog scale. Results: In 38 study completers (73.7% male; 65.8% white; mean age, 33.3 years), mean Drug Liking [E.sub.max] was significantly greater for phentermine versus pitolisant 35.6 mg (mean difference, 21.4; p &lt; 0.0001) and pitolisant 213.6 mg (mean difference, 19.7; p &lt; 0.0001). Drug Liking [E.sub.max] was similar for pitolisant (both doses) and placebo. Similarly, for key secondary measures of Overall Drug Liking and willingness to Take Drug Again, mean [E.sub.max] scores were significantly greater for phentermine versus pitolisant (both doses) and similar for pitolisant (both doses) versus placebo. The incidence of adverse events was 82.1% after phentermine HCl 60 mg, 72.5% after pitolisant 213.6 mg, 47.5% after pitolisant 35.6 mg, and 48.8% after placebo administration. Conclusions: In this study, pitolisant demonstrated significantly lower potential for abuse compared with phentermine and an overall profile similar to placebo; this suggests a low risk of abuse for pitolisant. Clinical Trial Registration: ClinicalTrials.gov NCT03152123. Determination of the abuse potential of pitolisant in healthy, nondependent recreational stimulant users. 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Methods: Nondependent, recreational stimulant users able to distinguish phentermine HCl 60 mg from placebo in a drug discrimination test were randomized in a four-period, double-blind, crossover design to receive single doses of pitolisant 35.6 mg (therapeutic dose), pitolisant 213.6 mg (supratherapeutic dose), phentermine HCl 60 mg, and placebo. The primary endpoint was maximum effect ([E.sub.max]) on the 100-point Drug Liking ("at this moment") visual analog scale. Results: In 38 study completers (73.7% male; 65.8% white; mean age, 33.3 years), mean Drug Liking [E.sub.max] was significantly greater for phentermine versus pitolisant 35.6 mg (mean difference, 21.4; p &lt; 0.0001) and pitolisant 213.6 mg (mean difference, 19.7; p &lt; 0.0001). Drug Liking [E.sub.max] was similar for pitolisant (both doses) and placebo. Similarly, for key secondary measures of Overall Drug Liking and willingness to Take Drug Again, mean [E.sub.max] scores were significantly greater for phentermine versus pitolisant (both doses) and similar for pitolisant (both doses) versus placebo. The incidence of adverse events was 82.1% after phentermine HCl 60 mg, 72.5% after pitolisant 213.6 mg, 47.5% after pitolisant 35.6 mg, and 48.8% after placebo administration. Conclusions: In this study, pitolisant demonstrated significantly lower potential for abuse compared with phentermine and an overall profile similar to placebo; this suggests a low risk of abuse for pitolisant. Clinical Trial Registration: ClinicalTrials.gov NCT03152123. Determination of the abuse potential of pitolisant in healthy, nondependent recreational stimulant users. 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Methods: Nondependent, recreational stimulant users able to distinguish phentermine HCl 60 mg from placebo in a drug discrimination test were randomized in a four-period, double-blind, crossover design to receive single doses of pitolisant 35.6 mg (therapeutic dose), pitolisant 213.6 mg (supratherapeutic dose), phentermine HCl 60 mg, and placebo. The primary endpoint was maximum effect ([E.sub.max]) on the 100-point Drug Liking ("at this moment") visual analog scale. Results: In 38 study completers (73.7% male; 65.8% white; mean age, 33.3 years), mean Drug Liking [E.sub.max] was significantly greater for phentermine versus pitolisant 35.6 mg (mean difference, 21.4; p &lt; 0.0001) and pitolisant 213.6 mg (mean difference, 19.7; p &lt; 0.0001). Drug Liking [E.sub.max] was similar for pitolisant (both doses) and placebo. Similarly, for key secondary measures of Overall Drug Liking and willingness to Take Drug Again, mean [E.sub.max] scores were significantly greater for phentermine versus pitolisant (both doses) and similar for pitolisant (both doses) versus placebo. The incidence of adverse events was 82.1% after phentermine HCl 60 mg, 72.5% after pitolisant 213.6 mg, 47.5% after pitolisant 35.6 mg, and 48.8% after placebo administration. Conclusions: In this study, pitolisant demonstrated significantly lower potential for abuse compared with phentermine and an overall profile similar to placebo; this suggests a low risk of abuse for pitolisant. Clinical Trial Registration: ClinicalTrials.gov NCT03152123. Determination of the abuse potential of pitolisant in healthy, nondependent recreational stimulant users. Key words: drug abuse; narcolepsy; pitolisant</abstract><pub>Oxford University Press</pub><doi>10.1093/sleep/zsz252</doi></addata></record>
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source Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Oxford University Press Journals All Titles (1996-Current); Alma/SFX Local Collection
subjects Adults
Analysis
Anti-obesity agents
Armodafinil
Care and treatment
Clobetasol
Drug abuse
Health aspects
Histamine
Narcolepsy
title Evaluation of the abuse potential of pitolisant, a selective [H.sub.3]-receptor antagonist/inverse agonist, for the treatment of adult patients with narcolepsy with or without cataplexy
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