跳至主要内容
临床试验/CTIS2023-505098-34-00
CTIS2023-505098-34-00招募中1 期

A Phase IV Longitudinal Study of SUBLOCADE (SUBUTEX Prolonged Release) Clinical Outcomes in Adults with Opioid Use Disorder (Opioid Dependence) - INDV-6000-406

Indivior Inc.0 个研究点目标入组 1,200 人开始时间: 2023年11月7日最近更新:

试验速览

阶段
1 期
状态
招募中
发起方
Indivior Inc.
入组人数
1,200

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 65+(—)
性别
All

入选标准

  • Is an adult = 18 years of age who has signed the ICF, Plans to receive additional SUBLOCADE injections and has initiated treatment for OUD/opioid dependence with SUBLOCADE within the last 3 months prior to Baseline Visit OR has completed an Indivior SUBLOCADE study (eg, INDV-6000-401, INDV-6000-405) and has received the last dose of SUBLOCADE on that study within 3 months prior to Baseline Visit

排除标准

  • Patient participating in any clinical trial requiring medical intervention, Patient currently using opioids to treat a diagnosis other than OUD/opioid dependence

研究者

发起方
Indivior Inc.

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