Indivior

37 total trials 36 completed

Indivior sponsors 37 registered US clinical trials on ClinicalTrials.gov, none currently recruiting, and 36 completed. 12 of these trials are in Phase 3-4 (later-stage) and 20 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Opioid-Related Disorders, with 4 trials.

Trial Pipeline

37 total, page 1 of 1

COMPLETED Phase 2

INDV-6001 Multiple-Dose Pharmacokinetic Study

NCT06576843

COMPLETED Phase 2

Proof of Concept and Dose-ranging Study of INDV-2000 in Individuals With Moderate to Severe Opioid Use Disorder

NCT06384157

COMPLETED

Evaluating the SUBLOCADE Treatment Exit Strategy

NCT05878210

COMPLETED

SUBLOCADE Long-term Outcomes

NCT05860959

COMPLETED Phase 1

Single Dose Study of [14C]-IDV184001AN ([14C]-IDV184001) in Healthy Adult Male Participants

NCT05974046

COMPLETED Phase 1

Study of Potential CYP3A4 Induction by INDV-2000 in Healthy Adults

NCT05694533

COMPLETED Phase 4

Evaluation of Buprenorphine Extended-Release Subcutaneous Injection at Alternative Injection Locations

NCT05704543

COMPLETED Phase 1

Study to Assess Repeated Doses of INDV-2000 in Healthy Volunteers and in Treatment Seeking Individuals With Opioid Use Disorder

NCT04976855

COMPLETED Phase 4

Buprenorphine Extended-Release Subcutaneous Injection (RBP-6000) in High-risk Users

NCT04995029

TERMINATED

An Observational Study of Environmental and Socioeconomic Factors in Opioid Recovery - Long Term

NCT04577144

COMPLETED Phase 1

INDV-2000 First in Human

NCT04413552

COMPLETED Phase 4

SUBLOCADE Rapid Initiation Extension Study

NCT04060654

COMPLETED Phase 4

SUBLOCADE Rapid Initiation Study

NCT03993392

COMPLETED Phase 4

Safety, Tolerability, Pharmacokinetics and Efficacy of 180 mg Subcutaneous Risperidone From 6 mg Oral Risperidone

NCT03978832

COMPLETED

Evaluation of Long-term Buprenorphine Plasma Exposure

NCT03752528

COMPLETED Phase 3

Open-Label Treatment Extension Study

NCT02896296

COMPLETED Phase 1

PK, Safety, and Tolerability Study of RBP-7000 of Different Molecular Weight Polymer in Subjects With Schizophrenia

NCT02687984

COMPLETED Phase 2

A Dose-Escalation Study to Determine the Maximum Tolerated Dose of Arbaclofen Placarbil in Subjects With Alcohol Use Disorder

NCT02511886

COMPLETED Phase 1

Pharmacokinetics, Safety, and Tolerability of Depot Buprenorphine at Three Different Molecular Weights in Treatment-Seeking Subjects With Opioid Use Disorder

NCT02559973

COMPLETED

An Observational Study of Environmental and SocioEconomic Factors in Opioid Recovery

NCT03604861

COMPLETED Phase 3

Safety and Tolerability Study of Depot Buprenorphine in Treatment Seeking Subjects With Opioid Use Disorder

NCT02510014

COMPLETED Phase 3

Treatment Seeking Participants With Opioid Use Disorders Assessing Tolerability of Depot Injections of Buprenorphine

NCT02357901

COMPLETED Phase 3

Long Term Study of RBP 7000 in the Treatment of Subjects With Schizophrenia

NCT02203838

COMPLETED Phase 3

Randomized, Double-blind, Placebo Controlled, Multi-center and Tolerability of RBP-7000 in Schizophrenia Patients

NCT02109562

COMPLETED Phase 4

Usability of Zubsolv Sublingual Tablets 5.7/1.4 to Suboxone Sublingual Film 8/2 In Buprenorphine/Naloxone Treated Opioid Dependent Population

NCT02038790

COMPLETED Phase 2

Multiple Dose Study of Blockade of Opioid Effects by Injections of Buprenorphine in Participants With Opioid Disorder

NCT02044094

COMPLETED Phase 2

A Randomized, 4-sequence, 2-period, Double-blind, Placebo Controlled Study With a DSM-IV-TR Diagnosis of Cocaine Abuse

NCT01846481

COMPLETED Phase 2

Multiple Dose Pharmacokinetics Depot Buprenorphine in Opioid-Dependent Subjects

NCT01738503

COMPLETED Phase 4

Single Dose Pharmacokinetics of Suboxone Study in Hepatic Impaired Subjects

NCT01846455

COMPLETED Phase 2

Multiple Ascending Dose Study of the Safety, Tolerability, Pharmacokinetic/Efficacy

NCT01677377

COMPLETED Phase 1

Single Ascending Dose Study of RBP-6000

NCT03002961

COMPLETED Phase 1

Single Ascending Dose Study of RBP-7000

NCT02768649

COMPLETED Phase 1

Single-dose, Study of RBP-6000 in Opioid Dependent Individuals

NCT02765867

COMPLETED Phase 1

First in Man Study of Safety, Tolerability and PK Profile of RBP-7000

NCT02765555

COMPLETED Phase 2

Induction of Opioid-Dependent Individuals Onto Buprenorphine and Buprenorphine/Naloxone

NCT00637000

COMPLETED Phase 2

Safety and Tolerability of Buprenorphine/Naloxone Film Strips

NCT00640835

COMPLETED Phase 2

A Study to Evaluate the Efficacy and Safety of Controlled Release Arbaclofen Placarbil (XP19986) in Patients With Gastroesophageal Reflux Disease

NCT00838396

Phase Distribution

PhaseTrial count
Phase 1 10
Phase 2 10
Phase 3 5
Phase 4 7

What the Pipeline for Indivior Shows

According to the ClinicalTrials.gov registry, Indivior is linked to 37 US clinical trials across every stage of research activity. Of those, 0 studies are currently recruiting, about 0% of the sponsor's indexed portfolio, and 36 are already marked complete, representing roughly 97% of the total.

The phase mix for Indivior reports 12 late-stage studies (Phase 3 and Phase 4 combined) and 20 earlier-phase studies (Phase 1 and Phase 2).

The top therapeutic focus area indexed for Indivior is Opioid-Related Disorders with 4 linked trials, and 3 other condition areas appear in the top list above.

How to read these pipeline numbers

Recruiting share is one of the more practical signals here: it reflects how much of a sponsor's research is presently open to new participants, while the completed share indicates the depth of finished work that has already contributed registry results. Both counts come directly from the public ClinicalTrials.gov dataset and are refreshed on the registry side; this page mirrors the latest data pull without altering it.

A portfolio weighted toward Phase 3 usually reflects an organization advancing candidates toward regulatory review, where the research centers on comparative efficacy and broader safety across larger populations. A heavier Phase 1 and Phase 2 tilt generally indicates exploratory work, safety, dosing, and early signal detection, and is common among research-forward sponsors that seed many early programs. Phase 4 entries, when present, track interventions already in real-world use and typically focus on long-term safety, effectiveness across subgroups, or formulation comparisons.

That distribution is a quick read of where the organization concentrates its research attention; it does not imply product availability, market share, or any clinical endorsement. All numbers on this page come from ClinicalTrials.gov maintained by the National Library of Medicine, and counts can shift as new studies are registered or existing ones update their status. This information is provided for reference and educational purposes only, not as medical, investment, or regulatory advice, verify current details directly with ClinicalTrials.gov before relying on any figure here.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page aggregates every registered trial from this sponsor, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.