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Trial Investigating the Efficacy and Safety of SCH 900435 (Org 25935) in Relapse Prevention in Participants With Alcohol Dependence (P05718) (OD-H)

2018年9月17日 更新者:Merck Sharp & Dohme LLC

A Prospective, Double-Blind, Placebo-Controlled Trial Investigating the Efficacy and Safety of SCH 900435 (Org 25935) in Relapse Prevention in Subjects With Alcohol Dependence.

The purpose of this study is to assess the effects of SCH 900435 (Org 25935, MK-8435) on heavy drinking, safety and tolerability of SCH 900435 in participants with alcohol dependence.

調査の概要

状態

終了しました

研究の種類

介入

入学 (実際)

141

段階

  • フェーズ2

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

18年~65年 (大人、高齢者)

健康ボランティアの受け入れ

いいえ

受講資格のある性別

全て

説明

Inclusion Criteria:

  • Provide written informed consent after the scope and nature of the investigation, have been explained to the participant before screening;
  • Diagnosis of alcohol dependence - meeting at least 5 out of 7 criteria according to Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition, Text Revision (DSM-IV-TR) specifier; one of which should be criterion 1 (tolerance) or 2 (withdrawal);
  • Primary complaints according to Mini-International Neuropsychiatric Interview (MINI) should be alcohol problems;
  • Participants must have gone through a detoxification program, have a clearly stated desire to stay abstinent and present at baseline with the following: be alcohol abstinent for at least 3 days, benzodiazepine free for at least 3 days, and a Clinical Institute Withdrawal Assessment (CIWA) score <10;
  • Age 18-65 years at screening;
  • Males, or females who are not of childbearing potential (i.e., surgically sterile, postmenopausal for at least one year) or who are non-pregnant, non-lactating and using a medically accepted method of contraception; these include condoms with or without a spermicidal agent, diaphragm or cervical cap with spermicide, medically prescribed intrauterine device (IUD), and hormonal contraceptives;
  • Body Mass Index (BMI) >16 kg/m^2;
  • Breath alcohol concentration < 0.02% (at screening and baseline)

Exclusion Criteria:

  • Participants requiring pharmacological treatment for a primary diagnosis of major depressive disorder, anxiety, panic disorder or social phobia;
  • Participants with psychotic disorders (according to MINI);
  • Participants with a medium or high suicidality risk (as assessed by MINI)
  • Active substance abuse (resulting in either physical or mental damage as defined by International Statistical Classification of Diseases and Related Health Problems, 10th revision [ICD10] or dependence other than alcohol (excluding nicotine) within 12 months prior to screening, e.g. cannabis, benzodiazepine, amphetamines, chlo(r)methiazole, opiates, cocaine, hallucinogens or other substances;
  • Use of one of the following drugs during the last 14 days prior to screening: cannabis, amphetamines, opiates, cocaine, hallucinogens;
  • Use of any medication that can have an effect on alcohol consumption within 30 days of study initiation, including naltrexone, acamprosate, disulfiram, ondansetron, topiramate, selective serotonin reuptake inhibitors (SSRIs), mirtazapine, varencicline, gabapentin, levetiracetam;
  • A clinically relevant visual disturbance, such as cataract, color blindness, macular degeneration, glaucoma or retinal disease;
  • Untreated or uncompensated clinically significant renal, endocrine, hepatic, respiratory, cardiovascular, hematological, immunological or cerebrovascular disease, malignancy, or other chronic and/or degenerative process at screening;
  • Any clinically meaningful abnormal laboratory, vital sign, physical examination or electrocardiogram (ECG) finding which, in the opinion of the investigator, may interfere with the interpretation of safety or efficacy evaluations;
  • QTc interval (Fridericia corrected) at screening >450 ms (male), >470 ms (female);
  • Serious neuropsychiatric condition that can impair judgment or cognitive function (including dementia or amnestic disorder) to an extent that providing informed consent or complying with treatment is precluded;
  • History or present evidence of epileptic disorders or withdrawal seizures;
  • History of substance withdrawal delirium;
  • Breast-feeding woman, or a positive result of urine pregnancy test (at screening), or plan to become pregnant during the course of the trial (females only);
  • Pending legal charges with the potential for incarceration, probation, or parole;
  • Homelessness (less than 2 months stable residence);
  • Participation in a clinical trial during the 3 months prior to screening.

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:4倍

武器と介入

参加者グループ / アーム
介入・治療
実験的:SCH 900435
Participants received SCH 900435 12 mg (as three SCH 900435 4 mg tablets) by mouth twice daily for 12 weeks.
tablets
他の名前:
  • Org 25935
  • MK-8435
プラセボコンパレーター:Placebo
Participants received matching placebo tablets by mouth twice daily for 12 weeks.
錠剤

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Percentage of Heavy Drinking Days
時間枠:12 weeks

Percentage of heavy drinking days was defined as days with ≥5 standard drinks for men and ≥4 standard drinks for women assessed by Alcohol Timeline Follow Back (TLFB) method. The Alcohol TLFB is a drinking assessment method that obtains estimates of daily drinking by means of an interview between investigator and participant. The TLFB assesses recent drinking behavior. On the TLFB, clients retrospectively estimate their daily alcohol consumption in standard drinks over a time period prior to the interview, and thus the measure provides quantitative estimates of alcohol use.

A drink is standardized to an equivalent to 25-30 cL of beer or wine coolers (5% alcohol), 12-15 cL of table wine (11-14% alcohol) and 4-6 cL of hard liquor/spirits (35-40% alcohol).

Percentage was calculated based on number of heavy drinking days divided by total number of days in the given 2-week interval.

12 weeks

二次結果の測定

結果測定
メジャーの説明
時間枠
Number of Drinks Per Drinking Day
時間枠:12 weeks
The amount of drinking was defined as drinks per drinking day (TLFB). Drinking day is a day on which an alcoholic drink is consumed, with 'day' being defined as the period between waking up and going to sleep; the end of a day may have crossed the time point of midnight.
12 weeks
Number of Relapses Into Heavy Drinking
時間枠:12 weeks
An alcohol relapse was defined as either a daily alcohol intake of 5 or more drinks for males and 4 or more drinks for females or an overall consumption of 14 drinks or more per week during at least 4 weeks (TLFB).
12 weeks
Number of Lapses Into Any Drinking
時間枠:12 weeks
An alcohol lapse was defined as any episode of alcohol consumption not classified as a relapse (TLFB).
12 weeks
Time to First Relapse Into Drinking
時間枠:12 weeks
Time to relapse was defined as the time to first relapse into heavy drinking (TLFB). A Hazard Ratio (SCH 900435/Placebo) of <1 means that SCH 900435 has a lower risk of relapsing as compared to Placebo.
12 weeks
Percentage of Abstinent Days
時間枠:12 weeks
Percentage of abstinent days is the percentage of study days in which participants remained abstinent during the treatment period.
12 weeks
Percentage of Participants With Complete Abstinence
時間枠:12 weeks
Percentage of total abstinence is the percentage of participants who remained abstinent during the entire treatment period.
12 weeks
Global Functioning: Clinical Global Impression (CGI) - Severity of Illness
時間枠:Day 84
The CGI scale is a standardized tool used by investigators to rate the severity of illness, taking into account the participant's clinical condition and the severity of side effects. The CGI scores could range from 1 to 7, with a lower score reflecting a better outcome.
Day 84
Global Functioning: CGI - Therapeutic Effect
時間枠:Day 84
The CGI scale is a standardized tool used by investigators to rate the efficacy of study drug (therapeutic effect), taking into account the participant's clinical condition and the severity of side effects. The CGI scores could range from 1 to 7, with a lower score reflecting a better outcome.
Day 84
Change From Baseline in Craving Visual Analog Scale (VAS) Score
時間枠:Baseline and Day 84
Rating of craving is included to assess a potential relationship between treatment and craving severity. Participants were asked to answer the question: "Over the past week, what has your desire or craving for an alcoholic beverage been at the time of day that you usually drink?" The 100 mm line of the VAS was anchored on the left by "No desire at all" and on the right by "Extreme desire". Participants marked a spot on the line where they felt their craving severity fit best. Craving VAS scores could range from 0 to 100, with a lower VAS score reflecting a better outcome.
Baseline and Day 84
Change From Baseline in Motivation VAS Score
時間枠:Baseline and Day 84
Participants were asked to answer the question: "Over the past week, how motivated were you to stay alcohol abstinent?" The 100 mm line of the VAS was anchored on the left by "No motivation at all" and on the right by "Extremely motivated". Motivation VAS scores could range from 0 to 100, with a higher score reflecting a better outcome.
Baseline and Day 84
Change From Baseline in Mood VAS Score
時間枠:Baseline and Day 84
Participants were asked to answer the question: "Over the past week, how did you feel?" The 100 mm line of the VAS was anchored on the left by "Extremely bad" and on the right by "Extremely good". Mood VAS scores could range from 0 to 100, with a higher VAS score reflecting a better outcome.
Baseline and Day 84
Number of Participants Who Experienced an Adverse Event (AE)
時間枠:Up to 16 weeks
An AE was defined as any unfavorable and unintended sign (including an abnormal laboratory finding), symptom, or disease temporally associated with the use of study drug, whether or not related to the study drug.
Up to 16 weeks
Number of Participants Who Discontinued Study Drug Due to an AE
時間枠:Up to 12 weeks
An AE was defined as any unfavorable and unintended sign (including an abnormal laboratory finding), symptom, or disease temporally associated with the use of study drug, whether or not related to the study drug.
Up to 12 weeks

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出版物と役立つリンク

研究に関する情報を入力する責任者は、自発的にこれらの出版物を提供します。これらは、研究に関連するあらゆるものに関するものである可能性があります。

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (実際)

2009年2月13日

一次修了 (実際)

2010年5月28日

研究の完了 (実際)

2010年7月8日

試験登録日

最初に提出

2008年9月30日

QC基準を満たした最初の提出物

2008年10月1日

最初の投稿 (見積もり)

2008年10月2日

学習記録の更新

投稿された最後の更新 (実際)

2018年10月16日

QC基準を満たした最後の更新が送信されました

2018年9月17日

最終確認日

2018年9月1日

詳しくは

本研究に関する用語

その他の研究ID番号

  • P05718
  • 2008-005318-35 (EudraCT番号)
  • 172009 (その他の識別子:Organon Protocol Number)
  • MK-8435-003 (その他の識別子:Merck Protocol Number)

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

はい

IPD プランの説明

https://www.merck.com/clinical-trials/pdf/ProcedureAccessClinicalTrialData.pdf

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。

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