Bausch Health Americas
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
Topically Applied IDP-118 Lotion and HP Monad Lotion in Subjects With Moderate to Severe Plaque Psoriasis
NCT03058744
Evaluation of the Safety, Systemic Pharmacokinetics, and Tolerability
NCT03063489
The Plecanatide Irritable Bowel Syndrome With Constipation Study (IBS-C)
NCT02387359
One Year Study of Rifaximin Delayed Release (DR) in Crohn's Disease
NCT02240108
A Bioequivalence Study Comparing a Single 1.5mL Dose of Brodalumab vs. Two Doses (1.0mL + 0.5mL) of Brodalumab
NCT02173392
One Year Study of Rifaximin Delayed Release (DR) Tablets in Crohn's Disease
NCT02240121
12-Week Study of Plecanatide for CIC (The National CIC3 Study)
NCT02122471
Study of Efficacy and Safety of Brodalumab in Subjects With Psoriatic Arthritis
NCT02024646
Study of Efficacy, Safety and Effect on Radiographic Progression of Brodalumab in Subjects With Psoriatic Arthritis
NCT02029495
Absorption and Systematic Pharmacokinetics of IDP-121 Lotion in Subjects With Acne Vulgaris
NCT02849860
Safety and Efficacy of IDP 118 in the Treatment of Plaque Psoriasis
NCT02045277
(C2013-0302) Safety and Efficacy of Escalating Doses of SAN-300 in Patients With Rheumatoid Arthritis
NCT02047604
EYEFILL® C. -US Viscoelastic Clinical Investigation
NCT02024711
12-Week Study of Plecanatide for CIC (The CIC3 Study)
NCT01982240
Dose-ranging Study to Assess Safety and Efficacy of SP-333 for the Treatment of Opioid-induced Constipation (OIC)
NCT01983306
Brodalumab Drug-Drug Interaction (DDI) and Intensive Pharmacodynamic (PK) Study in Psoriasis Subjects
NCT01937260
Open-label Extension (OLE) Study of Plecanatide for Chronic Idiopathic Constipation (CIC)
NCT01919697
Dose-ranging Study of Rifaximin Soluble Solid Dispersion (SSD) Tablets for the Prevention of Complications of Early Decompensated Liver Cirrhosis
NCT01904409
Efficacy, Safety, And Pharmacokinetics Of Rifaximin In Subjects With Severe Hepatic Impairment And Hepatic Encephalopathy
NCT01846663
The Safety/Efficacy of Rifaximin With/Without Lactulose in Participants With A History of Recurrent Hepatic Encephalopathy
NCT01842581
The Plecanatide Irritable Bowel Syndrome With Constipation Study (IBS-C)
NCT01722318
Clinical Study to Test the Efficacy and Safety of ACYC to Treat Moderate to Severe Acne
NCT01701024
Single Ascending Dose Study to Evaluate the Safety, Tolerability and Pharmacokinetics (PK) of SP-333 Tablets in Healthy Adult Subjects
NCT01705938
Efficacy and Safety of Brodalumab Compared With Placebo and Ustekinumab in Moderate to Severe Plaque Psoriasis Subjects
NCT01708629
Efficacy, Safety, and Withdrawal and Retreatment With Brodalumab in Moderate to Severe Plaque Psoriasis Subjects
NCT01708590
P3 Study Brodalumab in Treatment of Moderate to Severe Plaque Psoriasis
NCT01708603
Long Term Safety and Efficacy of Solesta® Injectable Bulking Agent for the Treatment of Fecal Incontinence (SoFI)
NCT01647906
Irritable Bowel Syndrome With Diarrhea (IBS-D) Rifaximin Re-Treatment Study
NCT01543178
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
The Plecanatide Chronic Idiopathic Constipation (CIC) Study
NCT01429987
AMG 827 in Subjects With Psoriatic Arthritis
NCT01516957
Safety and Efficacy of OsmoPrep® Tablets Versus HalfLytely® and Bisacodyl Tablet Bowel Prep Kit for Colon Cleansing
NCT01427296
Safety and Tolerability of Crofelemer for HIV-Associated Diarrhea
NCT01374490
The Safety and Tolerability of Budesonide Foam in Participants With Active Ulcerative Proctitis or Proctosigmoiditis
NCT01349673
A Study of a New Drug Treatment for Acne
NCT01326780
A Study That Evaluates the Decrease in Irritation When Using Additional Acne Treatment Products
NCT01313728
A Study of Oral Methylnaltrexone (MNTX) for the Treatment of Opioid-Induced Constipation (OIC) in Participants With Chronic, Non-Malignant Pain
NCT01186770
Mesalamine Granules for Irritable Bowel Syndrome (IBS) With Diarrhea
NCT01177410
A Study Comparing the Safety and Tolerability of Two Doses of Fipamezole in Adult Patients With Parkinson's Disease
NCT01149811
Evaluate the Pharmacokinetics (PK) of Methylnaltrexone (MNTX) in Healthy Adult Subjects
NCT01366326
A Study of Safety and Tolerability of Fipamezole in Adult Subjects With Parkinson's Disease Who Are Receiving Levodopa
NCT01140841
Metyrosine (Demser®) for the Treatment of Psychotic Disorders in Patients With Velocardiofacial Syndrome
NCT01127503
Study to Assess the Long-term Safety, Tolerability, and Efficacy of AMG 827 in Subjects With Psoriasis
NCT01101100
SP-304 Dose Ranging Study in Patients With Chronic Idiopathic Constipation
NCT01053962
Study Evaluating Two Dose Levels of Targretin Capsules in Participants With Refractory Cutaneous T-Cell Lymphoma (CTCL)
NCT01007448
Efficacy and Safety of Budesonide Foam for Participants With Active Mild to Moderate Ulcerative Proctitis or Proctosigmoiditis
NCT01008423
Efficacy and Safety of Budesonide Foam for Participants With Active Mild to Moderate Ulcerative Proctitis or Proctosigmoiditis
NCT01008410
Evaluation of Irritation That Potentially Could be Caused by Two Facial Gels Applied to Opposite Sides of the Face
NCT00952523
Evaluation of Irritation by Two Facial Gels Applied to Opposite Sides of the Face
NCT00919191
A Study of Different Use Regimens Using Two Acne Treatments
NCT00907257
Phase Distribution
| Phase | Trial count |
|---|---|
| Phase 1 | 31 |
| Phase 2 | 37 |
| Phase 3 | 68 |
| Phase 4 | 18 |
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.
Read our methodology - how this data is sourced, computed, and verified.
Related
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.