Either you have JavaScript disabled or your browser does not support Javascript . To work properly, this page requires JavaScript to be enabled.
How to enable JavaScript in your browser?

An Open-label, Multicentre Study to Evaluate the Pharmacokinetics, Safety, and Tolerability of Repeated Doses of INDV-6001 in Adults with Moderate to Severe Opioid Use Disorder

Next Previous
Trial Profile

An Open-label, Multicentre Study to Evaluate the Pharmacokinetics, Safety, and Tolerability of Repeated Doses of INDV-6001 in Adults with Moderate to Severe Opioid Use Disorder

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 20 Mar 2026

Price :
$35 *
Note:
  • Adis is an information provider.
  • Final gross price and currency may vary according to local VAT and billing address.
  • Your purchase entitles you to full access to the information contained in our trial profile at the time of purchase.
  • A link to download a PDF version of the trial profile will be included in your email receipt.

At a glance

  • Drugs Buprenorphine (Primary) ; Buprenorphine (Primary) ; Buprenorphine/naloxone
  • Indications Opioid-related disorders
  • Focus Pharmacokinetics
  • Sponsors Indivior

Most Recent Events

  • 16 Mar 2026 Status changed from active, no longer recruiting to completed.
  • 09 Dec 2025 Planned End Date changed from 1 Dec 2025 to 1 Jan 2026.
  • 09 Dec 2025 Planned primary completion date changed from 1 Dec 2025 to 1 Jan 2026.

You need to be a logged in or subscribed to view this content

Request demo (opens in a new window)
If your organization or you do not have a subscription, try one of the following: If your organization has a subscription, there are several access options, even while working remotely:
  • Working within your organization’s network
  • with username/password or try to via your institution
  • Persisted access using your organization’s identifier stored in your user browser for 90 days
Back to top