Varenicline as a treatment for cannabis use disorder: A placebo-controlled pilot trial
An efficacious pharmacotherapy for cannabis use disorder (CUD) has yet to be established. This study preliminarily evaluated the safety and efficacy of varenicline for CUD in a proof-of-concept clinical trial. Participants in this 6-week randomized, placebo-controlled pilot trial received either var...
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Veröffentlicht in: | Drug and alcohol dependence 2021-12, Vol.229 (Pt B), p.109111-109111, Article 109111 |
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creator | McRae-Clark, Aimee L. Gray, Kevin M. Baker, Nathaniel L. Sherman, Brian J. Squeglia, Lindsay Sahlem, Gregory L. Wagner, Amanda Tomko, Rachel |
description | An efficacious pharmacotherapy for cannabis use disorder (CUD) has yet to be established. This study preliminarily evaluated the safety and efficacy of varenicline for CUD in a proof-of-concept clinical trial.
Participants in this 6-week randomized, placebo-controlled pilot trial received either varenicline (n = 35) or placebo (n = 37), added to a brief motivational enhancement therapy intervention. Outcomes included cannabis withdrawal, cannabis abstinence, urine cannabinoid levels, percent cannabis use days, and cannabis sessions per day.
Both treatment groups noted significant decreases in self-reported cannabis withdrawal, percentage of days used, and use sessions per day during treatment compared to baseline. While this pilot trial was not powered to detect statistically significant between-group differences, participants randomized to varenicline evidenced numerically greater rates of self-reported abstinence at the final study visit [Week 6 intent-to-treat (ITT): Varenicline: 17.1% vs. Placebo: 5.4%; RR = 3.2 (95% CI: 0.7,14.7)]. End-of-treatment urine creatinine corrected cannabinoid levels were numerically lower in the varenicline group and higher in the placebo group compared to baseline [Change from baseline: Varenicline −1.7 ng/mg (95% CI: −4.1,0.8) vs. Placebo: 1.9 ng/mg (95% CI: −0.4,4.3); Δ = 3.5 (95% CI: 0.1,6.9)]. Adverse events related to study treatment did not reveal new safety signals.
Findings support the feasibility of conducting clinical trials of varenicline as a candidate pharmacotherapy for CUD, and indicate that a full-scale efficacy trial, powered based on effect sizes and variability yielded in this study, is warranted.
•Varenicline was evaluated for cannabis use disorder (CUD) in a placebo-controlled, pilot trial.•Greater reductions in urinary cannabinoids were observed with varenicline vs placebo.•Additional research is warranted to determine if varenicline improves cannabis use outcomes. |
doi_str_mv | 10.1016/j.drugalcdep.2021.109111 |
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Participants in this 6-week randomized, placebo-controlled pilot trial received either varenicline (n = 35) or placebo (n = 37), added to a brief motivational enhancement therapy intervention. Outcomes included cannabis withdrawal, cannabis abstinence, urine cannabinoid levels, percent cannabis use days, and cannabis sessions per day.
Both treatment groups noted significant decreases in self-reported cannabis withdrawal, percentage of days used, and use sessions per day during treatment compared to baseline. While this pilot trial was not powered to detect statistically significant between-group differences, participants randomized to varenicline evidenced numerically greater rates of self-reported abstinence at the final study visit [Week 6 intent-to-treat (ITT): Varenicline: 17.1% vs. Placebo: 5.4%; RR = 3.2 (95% CI: 0.7,14.7)]. End-of-treatment urine creatinine corrected cannabinoid levels were numerically lower in the varenicline group and higher in the placebo group compared to baseline [Change from baseline: Varenicline −1.7 ng/mg (95% CI: −4.1,0.8) vs. Placebo: 1.9 ng/mg (95% CI: −0.4,4.3); Δ = 3.5 (95% CI: 0.1,6.9)]. Adverse events related to study treatment did not reveal new safety signals.
Findings support the feasibility of conducting clinical trials of varenicline as a candidate pharmacotherapy for CUD, and indicate that a full-scale efficacy trial, powered based on effect sizes and variability yielded in this study, is warranted.
•Varenicline was evaluated for cannabis use disorder (CUD) in a placebo-controlled, pilot trial.•Greater reductions in urinary cannabinoids were observed with varenicline vs placebo.•Additional research is warranted to determine if varenicline improves cannabis use outcomes.</description><identifier>ISSN: 0376-8716</identifier><identifier>EISSN: 1879-0046</identifier><identifier>DOI: 10.1016/j.drugalcdep.2021.109111</identifier><identifier>PMID: 34655945</identifier><language>eng</language><publisher>Ireland: Elsevier B.V</publisher><subject>Abstinence ; Addiction ; Brief interventions ; Cannabinoids ; Cannabis ; Clinical research ; Clinical trials ; Creatinine ; Critical incidents ; Double-Blind Method ; Drug addiction ; Drug therapy ; Efficacy ; Feasibility ; Humans ; Marijuana ; Marijuana Abuse - drug therapy ; Motivational interviewing ; Pharmacology ; Pharmacotherapy ; Pilot Projects ; Placebos ; Safety ; Smoking Cessation ; Statistical analysis ; Substance abuse treatment ; Treatment ; Varenicline ; Varenicline - adverse effects</subject><ispartof>Drug and alcohol dependence, 2021-12, Vol.229 (Pt B), p.109111-109111, Article 109111</ispartof><rights>2021</rights><rights>Published by Elsevier B.V.</rights><rights>Copyright Elsevier Science Ltd. Dec 1, 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c507t-e86f59acb362629b0b5842aefbac40843758223693665fb7f65dafb487816fa03</citedby><cites>FETCH-LOGICAL-c507t-e86f59acb362629b0b5842aefbac40843758223693665fb7f65dafb487816fa03</cites><orcidid>0000-0001-5994-6894</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.drugalcdep.2021.109111$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,777,781,882,3537,27905,27906,30980,45976</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34655945$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>McRae-Clark, Aimee L.</creatorcontrib><creatorcontrib>Gray, Kevin M.</creatorcontrib><creatorcontrib>Baker, Nathaniel L.</creatorcontrib><creatorcontrib>Sherman, Brian J.</creatorcontrib><creatorcontrib>Squeglia, Lindsay</creatorcontrib><creatorcontrib>Sahlem, Gregory L.</creatorcontrib><creatorcontrib>Wagner, Amanda</creatorcontrib><creatorcontrib>Tomko, Rachel</creatorcontrib><title>Varenicline as a treatment for cannabis use disorder: A placebo-controlled pilot trial</title><title>Drug and alcohol dependence</title><addtitle>Drug Alcohol Depend</addtitle><description>An efficacious pharmacotherapy for cannabis use disorder (CUD) has yet to be established. This study preliminarily evaluated the safety and efficacy of varenicline for CUD in a proof-of-concept clinical trial.
Participants in this 6-week randomized, placebo-controlled pilot trial received either varenicline (n = 35) or placebo (n = 37), added to a brief motivational enhancement therapy intervention. Outcomes included cannabis withdrawal, cannabis abstinence, urine cannabinoid levels, percent cannabis use days, and cannabis sessions per day.
Both treatment groups noted significant decreases in self-reported cannabis withdrawal, percentage of days used, and use sessions per day during treatment compared to baseline. While this pilot trial was not powered to detect statistically significant between-group differences, participants randomized to varenicline evidenced numerically greater rates of self-reported abstinence at the final study visit [Week 6 intent-to-treat (ITT): Varenicline: 17.1% vs. Placebo: 5.4%; RR = 3.2 (95% CI: 0.7,14.7)]. End-of-treatment urine creatinine corrected cannabinoid levels were numerically lower in the varenicline group and higher in the placebo group compared to baseline [Change from baseline: Varenicline −1.7 ng/mg (95% CI: −4.1,0.8) vs. Placebo: 1.9 ng/mg (95% CI: −0.4,4.3); Δ = 3.5 (95% CI: 0.1,6.9)]. Adverse events related to study treatment did not reveal new safety signals.
Findings support the feasibility of conducting clinical trials of varenicline as a candidate pharmacotherapy for CUD, and indicate that a full-scale efficacy trial, powered based on effect sizes and variability yielded in this study, is warranted.
•Varenicline was evaluated for cannabis use disorder (CUD) in a placebo-controlled, pilot trial.•Greater reductions in urinary cannabinoids were observed with varenicline vs placebo.•Additional research is warranted to determine if varenicline improves cannabis use outcomes.</description><subject>Abstinence</subject><subject>Addiction</subject><subject>Brief interventions</subject><subject>Cannabinoids</subject><subject>Cannabis</subject><subject>Clinical research</subject><subject>Clinical trials</subject><subject>Creatinine</subject><subject>Critical incidents</subject><subject>Double-Blind Method</subject><subject>Drug addiction</subject><subject>Drug therapy</subject><subject>Efficacy</subject><subject>Feasibility</subject><subject>Humans</subject><subject>Marijuana</subject><subject>Marijuana Abuse - drug therapy</subject><subject>Motivational interviewing</subject><subject>Pharmacology</subject><subject>Pharmacotherapy</subject><subject>Pilot Projects</subject><subject>Placebos</subject><subject>Safety</subject><subject>Smoking Cessation</subject><subject>Statistical analysis</subject><subject>Substance abuse treatment</subject><subject>Treatment</subject><subject>Varenicline</subject><subject>Varenicline - adverse effects</subject><issn>0376-8716</issn><issn>1879-0046</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>7QJ</sourceid><recordid>eNqFUUtrFTEUDqLYa_UvSMD13CaTx2RcCLW0VSh0o92GTHJSc8lNxmSm4L83l1urrno2gXO-F_kQwpRsKaHybLd1Zb030TqYtz3paVuPlNIXaEPVMHaEcPkSbQgbZKcGKk_Qm1p3pI0cyWt0wrgUYuRig-7uTIEUbAwJsKnY4KWAWfaQFuxzwdakZKZQ8VoBu1BzcVA-4nM8R2Nhyp3NaSk5RnB4DjEvjR9MfIteeRMrvHt8T9H3q8tvF1-6m9vrrxfnN50VZFg6UNKL0diJyV7240QmoXhvwE_GcqI4G4TqeyZHJqXw0-ClcMZPXA2KSm8IO0WfjrrzOu3B2Ra7mKjnEvam_NLZBP3_JYUf-j4_aNUECZNN4MOjQMk_V6iL3uW1pJZZt0SMcMbpwUYdUbbkWgv4JwdK9KERvdN_G9GHRvSxkUZ9_2_CJ-KfChrg8xEA7Z8eAhRdbYBkwYUCdtEuh-ddfgNuYKK9</recordid><startdate>20211201</startdate><enddate>20211201</enddate><creator>McRae-Clark, Aimee L.</creator><creator>Gray, Kevin M.</creator><creator>Baker, Nathaniel L.</creator><creator>Sherman, Brian J.</creator><creator>Squeglia, Lindsay</creator><creator>Sahlem, Gregory L.</creator><creator>Wagner, Amanda</creator><creator>Tomko, Rachel</creator><general>Elsevier B.V</general><general>Elsevier Science Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QJ</scope><scope>7TK</scope><scope>7U7</scope><scope>C1K</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-5994-6894</orcidid></search><sort><creationdate>20211201</creationdate><title>Varenicline as a treatment for cannabis use disorder: A placebo-controlled pilot trial</title><author>McRae-Clark, Aimee L. ; Gray, Kevin M. ; Baker, Nathaniel L. ; Sherman, Brian J. ; Squeglia, Lindsay ; Sahlem, Gregory L. ; Wagner, Amanda ; Tomko, Rachel</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c507t-e86f59acb362629b0b5842aefbac40843758223693665fb7f65dafb487816fa03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Abstinence</topic><topic>Addiction</topic><topic>Brief interventions</topic><topic>Cannabinoids</topic><topic>Cannabis</topic><topic>Clinical research</topic><topic>Clinical trials</topic><topic>Creatinine</topic><topic>Critical incidents</topic><topic>Double-Blind Method</topic><topic>Drug addiction</topic><topic>Drug therapy</topic><topic>Efficacy</topic><topic>Feasibility</topic><topic>Humans</topic><topic>Marijuana</topic><topic>Marijuana Abuse - drug therapy</topic><topic>Motivational interviewing</topic><topic>Pharmacology</topic><topic>Pharmacotherapy</topic><topic>Pilot Projects</topic><topic>Placebos</topic><topic>Safety</topic><topic>Smoking Cessation</topic><topic>Statistical analysis</topic><topic>Substance abuse treatment</topic><topic>Treatment</topic><topic>Varenicline</topic><topic>Varenicline - adverse effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>McRae-Clark, Aimee L.</creatorcontrib><creatorcontrib>Gray, Kevin M.</creatorcontrib><creatorcontrib>Baker, Nathaniel L.</creatorcontrib><creatorcontrib>Sherman, Brian J.</creatorcontrib><creatorcontrib>Squeglia, Lindsay</creatorcontrib><creatorcontrib>Sahlem, Gregory L.</creatorcontrib><creatorcontrib>Wagner, Amanda</creatorcontrib><creatorcontrib>Tomko, Rachel</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Applied Social Sciences Index & Abstracts (ASSIA)</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Drug and alcohol dependence</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>McRae-Clark, Aimee L.</au><au>Gray, Kevin M.</au><au>Baker, Nathaniel L.</au><au>Sherman, Brian J.</au><au>Squeglia, Lindsay</au><au>Sahlem, Gregory L.</au><au>Wagner, Amanda</au><au>Tomko, Rachel</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Varenicline as a treatment for cannabis use disorder: A placebo-controlled pilot trial</atitle><jtitle>Drug and alcohol dependence</jtitle><addtitle>Drug Alcohol Depend</addtitle><date>2021-12-01</date><risdate>2021</risdate><volume>229</volume><issue>Pt B</issue><spage>109111</spage><epage>109111</epage><pages>109111-109111</pages><artnum>109111</artnum><issn>0376-8716</issn><eissn>1879-0046</eissn><abstract>An efficacious pharmacotherapy for cannabis use disorder (CUD) has yet to be established. This study preliminarily evaluated the safety and efficacy of varenicline for CUD in a proof-of-concept clinical trial.
Participants in this 6-week randomized, placebo-controlled pilot trial received either varenicline (n = 35) or placebo (n = 37), added to a brief motivational enhancement therapy intervention. Outcomes included cannabis withdrawal, cannabis abstinence, urine cannabinoid levels, percent cannabis use days, and cannabis sessions per day.
Both treatment groups noted significant decreases in self-reported cannabis withdrawal, percentage of days used, and use sessions per day during treatment compared to baseline. While this pilot trial was not powered to detect statistically significant between-group differences, participants randomized to varenicline evidenced numerically greater rates of self-reported abstinence at the final study visit [Week 6 intent-to-treat (ITT): Varenicline: 17.1% vs. Placebo: 5.4%; RR = 3.2 (95% CI: 0.7,14.7)]. End-of-treatment urine creatinine corrected cannabinoid levels were numerically lower in the varenicline group and higher in the placebo group compared to baseline [Change from baseline: Varenicline −1.7 ng/mg (95% CI: −4.1,0.8) vs. Placebo: 1.9 ng/mg (95% CI: −0.4,4.3); Δ = 3.5 (95% CI: 0.1,6.9)]. Adverse events related to study treatment did not reveal new safety signals.
Findings support the feasibility of conducting clinical trials of varenicline as a candidate pharmacotherapy for CUD, and indicate that a full-scale efficacy trial, powered based on effect sizes and variability yielded in this study, is warranted.
•Varenicline was evaluated for cannabis use disorder (CUD) in a placebo-controlled, pilot trial.•Greater reductions in urinary cannabinoids were observed with varenicline vs placebo.•Additional research is warranted to determine if varenicline improves cannabis use outcomes.</abstract><cop>Ireland</cop><pub>Elsevier B.V</pub><pmid>34655945</pmid><doi>10.1016/j.drugalcdep.2021.109111</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0001-5994-6894</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Abstinence Addiction Brief interventions Cannabinoids Cannabis Clinical research Clinical trials Creatinine Critical incidents Double-Blind Method Drug addiction Drug therapy Efficacy Feasibility Humans Marijuana Marijuana Abuse - drug therapy Motivational interviewing Pharmacology Pharmacotherapy Pilot Projects Placebos Safety Smoking Cessation Statistical analysis Substance abuse treatment Treatment Varenicline Varenicline - adverse effects |
title | Varenicline as a treatment for cannabis use disorder: A placebo-controlled pilot trial |
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