Bausch Health Americas

168 total trials 6 currently recruiting 144 completed

Bausch Health Americas sponsors 168 registered US clinical trials on ClinicalTrials.gov, 6 of them currently recruiting, and 144 completed. 86 of these trials are in Phase 3-4 (later-stage) and 68 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Acne Vulgaris, with 6 trials.

Trial Pipeline

168 total, page 3 of 4

COMPLETED Phase 2

A Study of Acne Treatment in Children Ages 9 to 11

NCT00907335

COMPLETED Phase 3

Study Evaluating Long-Term Safety of MOA-728 in Participants With Opioid-Induced Constipation

NCT00804141

COMPLETED Phase 3

(CB-01-02/04) Extension Study of Budesonide Multi-Matrix System (MMX) 6 mg in Maintenance Of Remission In Patients With Ulcerative Colitis.

NCT00801723

COMPLETED Phase 4

Safety of Subcutaneous Methylnaltrexone for Opioid-Induced Constipation in Patients With Advanced Illness

NCT00672139

COMPLETED Phase 3

Rifaximin 3 Times/Day (TID) for Non-Constipation Irritable Bowel Syndrome (IBS)

NCT00724126

COMPLETED Phase 3

Rifaximin 3 Times/Day (TID) for Non-Constipation Irritable Bowel Syndrome (IBS)

NCT00731679

COMPLETED Phase 3

(CB-01-02/01) Randomized Placebo Controlled Trial of Budesonide-multi-matrix System (MMX™) 6 mg and 9 mg in Patients With Ulcerative Colitis

NCT00679432

COMPLETED Phase 4

Study Evaluating Subcutaneous Methylnaltrexone For Treatment Of Opioid-Induced Constipation In Patients With Advanced Illness

NCT00672477

COMPLETED Phase 1

PK Study of Encapsulated Mesalamine Granules in Healthy Volunteers

NCT00622375

COMPLETED Phase 4

Evaluation of Irritation That Could be Caused by Two Facial Gels Applied to Opposite Sides of the Face.

NCT00714714

COMPLETED Phase 2

Study of Subcutaneous Methylnaltrexone (MNTX) in the Treatment of Opioid-Induced Constipation During Rehabilitation After Orthopedic Procedures

NCT00640146

COMPLETED Phase 3

A Study Evaluating Intravenous (IV) MOA-728 for the Treatment of Postoperative Ileus (POI) in Participants After Ventral Hernia Repair

NCT00528970

COMPLETED Phase 3

Safety and Effectiveness of 3 Doses of Crofelemer Compared to Placebo in the Treatment of HIV Associated Diarrhea

NCT00547898

COMPLETED Phase 2

Safety/Efficacy Study of Retigabine vs. Placebo in Post-Herpetic Neuralgia (PHN)

NCT00612105

COMPLETED Phase 2

Study Evaluating Oral MOA-728 For The Treatment Of OIBD In Subjects With Chronic Non-Malignant Pain

NCT00547586

COMPLETED Phase 3

Study Evaluating Subcutaneous MOA-728 for the Treatment of Opioid-Induced Constipation (OIC) in Subjects With Chronic Non-Malignant Pain

NCT00529087

COMPLETED Phase 1

Study Evaluating the Safety and Tolerability of a New Intravenous Formulation of MOA-728 in Healthy Subjects

NCT00464802

COMPLETED Phase 3

Safety and Tolerability Study of Rifaximin in Participants With a History of Hepatic Encephalopathy

NCT00686920

COMPLETED Phase 1

Study Evaluating MOA-728 in Subjects on Stable Methadone Maintenance

NCT00447811

COMPLETED Phase 1

Study Evaluating the Effects of MOA-728 on Cardiac Repolarization in Healthy Subjects

NCT00434395

COMPLETED Phase 1

Double-Blind, Double-Dummy, 2-Period Crossover of a 20-Minute Versus a 4-hour IV of MOA-728 in Stable Methadone Subjects

NCT00444158

COMPLETED Phase 2

Taribavirin Phase 2 Dose Finding Study for the Treatment of Hepatitis C Virus (HCV)

NCT00446134

COMPLETED Phase 1

Effect of Cimetidine on the Single-Dose PK of IV- Administered MNTX

NCT01366378

COMPLETED Phase 3

Study Evaluating IV Methylnaltrexone for the Treatment of Post Operative Ileus

NCT00387309

COMPLETED Phase 3

Study of Intravenous (IV) Methylnaltrexone Bromide (MNTX) in the Treatment of Post-Operative Ileus (POI)

NCT00401375

COMPLETED Phase 3

Open-Label, Long-term Balsalziade Disodium Tablet Ulcerative Colitis Study

NCT00486031

COMPLETED Phase 2

Diarrhea Predominant Irritable Bowel Syndrome in Females

NCT00461526

COMPLETED Phase 1

Study of Pharmacokinetics, Safety and Tolerability of Intravenous Methylnaltrexone Bromide

NCT01366365

COMPLETED Phase 1

Comparisons Of The Bioavailability And Pharmacodynamics Of Various Formulations Of MOA-728 In Subjects On Methadone

NCT00398502

COMPLETED NA

A Randomized, Blinded, Multicenter Study to Evaluate NASHA/Dx for the Treatment of Fecal Incontinence

NCT00605826

COMPLETED Phase 2

Study Evaluating Oral MOA-728 for the Treatment of Opioid-Induced Bowel Dysfunction (OIBD) in Subjects With Chronic Non-Malignant Pain

NCT00366431

COMPLETED Phase 1

Bioequivalence Study in Healthy Volunteers

NCT00387985

COMPLETED Phase 1

Dose Ranging Study in Healthy Methadone Maintenance Subjects

NCT00387491

COMPLETED Phase 3

Balsalazide Disodium vs. Mesalamine in Mildly to Moderately Active Ulcerative Colitis

NCT00408174

COMPLETED Phase 1

Study Evaluating the Safety of MOA-728 Administered Orally to Healthy Subjects

NCT00311350

COMPLETED Phase 1

Effects of MNTX on CYP450 2D6 in Metabolizers of Dextromethorphan

NCT01367535

COMPLETED Phase 3

Long-Term Safety and Tolerability of Mesalamine Pellets in Participants With Ulcerative Colitis in Remission

NCT00326209

COMPLETED Phase 2

Study to Assess the Efficacy and Safety of Rifaximin Administered BID in the Treatment of Patients With Diarrhea-Associated Irritable Bowel Syndrome

NCT00269412

COMPLETED Phase 3

New Tablet Formulation and Dosing Regimen of Balsalazide Disodium in Mildly to Moderately Active Ulcerative Colitis

NCT00269438

COMPLETED Phase 3

Prevention of Travelers' Diarrhea in Subjects Traveling Outside the U.S.

NCT00328380

COMPLETED Phase 3

A Trial to Compare Xifaxan to Vancomycin for the Treatment of Clostridium Difficile-Associated Diarrhea (CDAD)

NCT00269399

TERMINATED Phase 2

Viral Kinetic Study With Viramidine in Therapy-Naive Patients With Chronic Hepatitis C

NCT00305383

COMPLETED

Facial Lipoatrophy Correction Experience With SCULPTRA ("FACES" Study)

NCT00360932

COMPLETED Phase 1

Study of the Pharmacokinetics of Intravenous Administered 14C-MNTX

NCT01367483

COMPLETED Phase 2

A Study of Crofelemer to Treat Diarrhea Irritable Bowel Syndrome

NCT00101725

COMPLETED Phase 3

Mesalamine Pellet Formulation to Maintain Remission of Mild to Moderate Ulcerative Colitis

NCT00744016

COMPLETED Phase 3

Mesalamine Pellet to Maintain Remission of Mild to Moderate Ulcerative Colitis

NCT00767728

COMPLETED Phase 1

Effect of Methylnaltrexone (MNTX) on Electrocardiogram (ECG) Parameters and Cardiac Repolarization

NCT01363323

COMPLETED Phase 3

DL6049 Versus Cosmoplast in the Treatment of Nasolabial Fold Wrinkles, Long Term Follow-up

NCT00444353

COMPLETED Phase 3

DL6049 vs CosmoPlast in the Treatment of Nasolabial Fold Wrinkles

NCT00444210

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What the Pipeline for Bausch Health Americas Shows

According to the ClinicalTrials.gov registry, Bausch Health Americas is linked to 168 US clinical trials across every stage of research activity. Of those, 6 studies are currently recruiting, about 4% of the sponsor's indexed portfolio, and 144 are already marked complete, representing roughly 86% of the total.

The phase mix for Bausch Health Americas reports 86 late-stage studies (Phase 3 and Phase 4 combined) and 68 earlier-phase studies (Phase 1 and Phase 2).

The top therapeutic focus area indexed for Bausch Health Americas is Acne Vulgaris with 6 linked trials, and 9 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.