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 2 of 4

COMPLETED Phase 1

Topically Applied IDP-118 Lotion and HP Monad Lotion in Subjects With Moderate to Severe Plaque Psoriasis

NCT03058744

COMPLETED Phase 1

Evaluation of the Safety, Systemic Pharmacokinetics, and Tolerability

NCT03063489

COMPLETED Phase 3

The Plecanatide Irritable Bowel Syndrome With Constipation Study (IBS-C)

NCT02387359

TERMINATED Phase 3

One Year Study of Rifaximin Delayed Release (DR) in Crohn's Disease

NCT02240108

COMPLETED Phase 1

A Bioequivalence Study Comparing a Single 1.5mL Dose of Brodalumab vs. Two Doses (1.0mL + 0.5mL) of Brodalumab

NCT02173392

TERMINATED Phase 3

One Year Study of Rifaximin Delayed Release (DR) Tablets in Crohn's Disease

NCT02240121

COMPLETED Phase 3

12-Week Study of Plecanatide for CIC (The National CIC3 Study)

NCT02122471

COMPLETED Phase 3

Study of Efficacy and Safety of Brodalumab in Subjects With Psoriatic Arthritis

NCT02024646

TERMINATED Phase 3

Study of Efficacy, Safety and Effect on Radiographic Progression of Brodalumab in Subjects With Psoriatic Arthritis

NCT02029495

COMPLETED Phase 1

Absorption and Systematic Pharmacokinetics of IDP-121 Lotion in Subjects With Acne Vulgaris

NCT02849860

COMPLETED Phase 2

Safety and Efficacy of IDP 118 in the Treatment of Plaque Psoriasis

NCT02045277

COMPLETED Phase 2

(C2013-0302) Safety and Efficacy of Escalating Doses of SAN-300 in Patients With Rheumatoid Arthritis

NCT02047604

COMPLETED NA

EYEFILL® C. -US Viscoelastic Clinical Investigation

NCT02024711

COMPLETED Phase 3

12-Week Study of Plecanatide for CIC (The CIC3 Study)

NCT01982240

COMPLETED Phase 2

Dose-ranging Study to Assess Safety and Efficacy of SP-333 for the Treatment of Opioid-induced Constipation (OIC)

NCT01983306

COMPLETED Phase 1

Brodalumab Drug-Drug Interaction (DDI) and Intensive Pharmacodynamic (PK) Study in Psoriasis Subjects

NCT01937260

COMPLETED Phase 3

Open-label Extension (OLE) Study of Plecanatide for Chronic Idiopathic Constipation (CIC)

NCT01919697

COMPLETED Phase 2

Dose-ranging Study of Rifaximin Soluble Solid Dispersion (SSD) Tablets for the Prevention of Complications of Early Decompensated Liver Cirrhosis

NCT01904409

TERMINATED Phase 4

Efficacy, Safety, And Pharmacokinetics Of Rifaximin In Subjects With Severe Hepatic Impairment And Hepatic Encephalopathy

NCT01846663

COMPLETED Phase 4

The Safety/Efficacy of Rifaximin With/Without Lactulose in Participants With A History of Recurrent Hepatic Encephalopathy

NCT01842581

COMPLETED Phase 2

The Plecanatide Irritable Bowel Syndrome With Constipation Study (IBS-C)

NCT01722318

COMPLETED Phase 3

Clinical Study to Test the Efficacy and Safety of ACYC to Treat Moderate to Severe Acne

NCT01701024

COMPLETED Phase 1

Single Ascending Dose Study to Evaluate the Safety, Tolerability and Pharmacokinetics (PK) of SP-333 Tablets in Healthy Adult Subjects

NCT01705938

TERMINATED Phase 3

Efficacy and Safety of Brodalumab Compared With Placebo and Ustekinumab in Moderate to Severe Plaque Psoriasis Subjects

NCT01708629

TERMINATED Phase 3

Efficacy, Safety, and Withdrawal and Retreatment With Brodalumab in Moderate to Severe Plaque Psoriasis Subjects

NCT01708590

TERMINATED Phase 3

P3 Study Brodalumab in Treatment of Moderate to Severe Plaque Psoriasis

NCT01708603

COMPLETED

Long Term Safety and Efficacy of Solesta® Injectable Bulking Agent for the Treatment of Fecal Incontinence (SoFI)

NCT01647906

COMPLETED Phase 3

Irritable Bowel Syndrome With Diarrhea (IBS-D) Rifaximin Re-Treatment Study

NCT01543178

COMPLETED Phase 3

Randomized Placebo-Controlled Trial of Budesonide Multi-Matrix System (MMX®) 9 Milligrams (mg) in Participants With Ulcerative Colitis Currently on a 5-Aminosalicylic Acid (5-ASA)

NCT01532648

COMPLETED Phase 2

The Plecanatide Chronic Idiopathic Constipation (CIC) Study

NCT01429987

TERMINATED Phase 2

AMG 827 in Subjects With Psoriatic Arthritis

NCT01516957

COMPLETED Phase 4

Safety and Efficacy of OsmoPrep® Tablets Versus HalfLytely® and Bisacodyl Tablet Bowel Prep Kit for Colon Cleansing

NCT01427296

COMPLETED Phase 3

Safety and Tolerability of Crofelemer for HIV-Associated Diarrhea

NCT01374490

TERMINATED Phase 3

The Safety and Tolerability of Budesonide Foam in Participants With Active Ulcerative Proctitis or Proctosigmoiditis

NCT01349673

COMPLETED Phase 2

A Study of a New Drug Treatment for Acne

NCT01326780

COMPLETED Phase 4

A Study That Evaluates the Decrease in Irritation When Using Additional Acne Treatment Products

NCT01313728

COMPLETED Phase 3

A Study of Oral Methylnaltrexone (MNTX) for the Treatment of Opioid-Induced Constipation (OIC) in Participants With Chronic, Non-Malignant Pain

NCT01186770

COMPLETED Phase 2

Mesalamine Granules for Irritable Bowel Syndrome (IBS) With Diarrhea

NCT01177410

COMPLETED

A Study Comparing the Safety and Tolerability of Two Doses of Fipamezole in Adult Patients With Parkinson's Disease

NCT01149811

COMPLETED Phase 1

Evaluate the Pharmacokinetics (PK) of Methylnaltrexone (MNTX) in Healthy Adult Subjects

NCT01366326

COMPLETED

A Study of Safety and Tolerability of Fipamezole in Adult Subjects With Parkinson's Disease Who Are Receiving Levodopa

NCT01140841

TERMINATED Phase 2

Metyrosine (Demser®) for the Treatment of Psychotic Disorders in Patients With Velocardiofacial Syndrome

NCT01127503

TERMINATED Phase 2

Study to Assess the Long-term Safety, Tolerability, and Efficacy of AMG 827 in Subjects With Psoriasis

NCT01101100

COMPLETED Phase 2

SP-304 Dose Ranging Study in Patients With Chronic Idiopathic Constipation

NCT01053962

COMPLETED Phase 4

Study Evaluating Two Dose Levels of Targretin Capsules in Participants With Refractory Cutaneous T-Cell Lymphoma (CTCL)

NCT01007448

COMPLETED Phase 3

Efficacy and Safety of Budesonide Foam for Participants With Active Mild to Moderate Ulcerative Proctitis or Proctosigmoiditis

NCT01008423

COMPLETED Phase 3

Efficacy and Safety of Budesonide Foam for Participants With Active Mild to Moderate Ulcerative Proctitis or Proctosigmoiditis

NCT01008410

COMPLETED Phase 4

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

NCT00952523

COMPLETED Phase 4

Evaluation of Irritation by Two Facial Gels Applied to Opposite Sides of the Face

NCT00919191

COMPLETED Phase 4

A Study of Different Use Regimens Using Two Acne Treatments

NCT00907257

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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.