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Efficacy and Safety of a Nicotine Mouth Spray for Smoking Cessation: A Randomized, Multicenter, Controlled Study in a Naturalistic Setting.
Nides, Mitchell; Danielsson, Tobias; Saunders, Frederick; Perfekt, Roland; Kapikian, Roxanne; Solla, Janice; Leischow, Scott J; Myers, Andrew.
Afiliação
  • Nides M; Los Angeles Clinical Trials, Burbank, CA.
  • Danielsson T; McNeil AB, Helsingborg, Sweden.
  • Saunders F; GSK Consumer Healthcare, Warren, NJ.
  • Perfekt R; McNeil AB, Helsingborg, Sweden.
  • Kapikian R; GSK Consumer Healthcare, Warren, NJ.
  • Solla J; McNeil Consumer Healthcare Division, Johnson & Johnson Consumer Inc., Fort Washington, PA.
  • Leischow SJ; Mayo Clinic Arizona, Scottsdale, AZ.
  • Myers A; McNeil Consumer Healthcare Division, Johnson & Johnson Consumer Inc., Fort Washington, PA.
Nicotine Tob Res ; 22(3): 339-345, 2020 03 16.
Article em En | MEDLINE | ID: mdl-30452732
ABSTRACT

BACKGROUND:

Nicotine replacement therapy (NRT) has been demonstrated to be an effective pharmacological treatment for smoking cessation, and most types of NRT have been approved as over-the-counter (OTC) medications. In an effort to create a fast-acting, flexible, and discreet NRT, a nicotine mouth spray (NMS) has been developed. This study was designed to assess the efficacy and safety of NMS in a naturalistic setting in the United States.

METHODS:

This was a multicenter, randomized, double-blind, placebo-controlled, parallel-group, 26-week study in 1198 smokers motivated to quit. The study was designed to resemble an OTC environment, and thus included limited intervention, limited motivational screening, and no behavioral support. The primary efficacy endpoint was carbon monoxide-verified, self-reported continuous abstinence from smoking from week 2 until week 6. The safety of NMS was assessed by measuring vital signs, visual mouth inspection, and collection of subject-reported adverse events (AEs).

RESULTS:

The percentage of subjects with carbon monoxide-verified continuous abstinence from week 2 to week 6 was statistically significantly greater in the NMS group compared with the placebo group (5.0% vs. 2.5%, p = .021). Statistically significant treatment effects for the NMS were maintained throughout the 26-week period. The study medications were generally well tolerated. The severity of AEs was similar for both treatment groups, and most AEs were of mild or moderate severity.

CONCLUSIONS:

These study results demonstrate that the NMS is an effective and safe smoking cessation option for smokers motivated to quit, even in a naturalistic setting and without behavioral support. IMPLICATIONS This study demonstrated the safety, efficacy, and acceptability of an NMS in an OTC environment with no behavioral counseling or support. It provides an additional option for smokers motivated to quit. TRIAL REGISTRATION ClinicalTrials.gov (number NCT02355665).
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fumar / Abandono do Hábito de Fumar / Agonistas Nicotínicos / Dispositivos para o Abandono do Uso de Tabaco / Nicotina Tipo de estudo: Clinical_trials Limite: Female / Humans / Male / Middle aged Idioma: En Revista: Nicotine Tob Res Assunto da revista: SAUDE PUBLICA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Canadá

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fumar / Abandono do Hábito de Fumar / Agonistas Nicotínicos / Dispositivos para o Abandono do Uso de Tabaco / Nicotina Tipo de estudo: Clinical_trials Limite: Female / Humans / Male / Middle aged Idioma: En Revista: Nicotine Tob Res Assunto da revista: SAUDE PUBLICA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Canadá