Wyeth is now a wholly owned subsidiary of Pfizer

167 total trials 139 completed

Wyeth is now a wholly owned subsidiary of Pfizer sponsors 167 registered US clinical trials on ClinicalTrials.gov, none currently recruiting, and 139 completed. 53 of these trials are in Phase 3-4 (later-stage) and 102 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Healthy, with 5 trials.

Trial Pipeline

167 total, page 3 of 4

COMPLETED Phase 3

Study Evaluating Pantoprazole in Children With Gastroesophageal Reflux Disease (GERD)

NCT00300755

COMPLETED Phase 1

Study Evaluating the Safety of HCV-796 in Subjects With Liver Disease and in Healthy Adults

NCT00314054

COMPLETED Phase 3

Study Evaluating the Pharmacokinetics of Venlafaxine ER and Desvenlafaxine SR in Healthy Subjects

NCT00329186

COMPLETED Phase 1

Study Evaluating the Effects of Multiple Oral Doses of ERB-041 on Cardiac Repolarization in Healthy Subjects

NCT00316459

COMPLETED Phase 3

Study Evaluating the Effects of DVS SR and Paroxetine on the Pharmacokinetics of Desipramine in Healthy Subjects

NCT00329147

COMPLETED Phase 2

Study Evaluating the Safety and Efficacy of ERB-041 on Reduction of Symptoms Associated With Endometriosis in Reproductive-Aged Women

NCT00318500

COMPLETED Phase 3

Study Evaluating B-Domain Deleted Recombinant Factor VIII (BDDrFVIII, ReFacto AF) in Patients With Hemophilia A Undergoing Elective Major Surgery

NCT00243659

COMPLETED Phase 3

Open Label Safety Study of Enteric-Coated Spheroid Suspension in Infants Aged Less Than 12 Months With Presumed Gastroesophageal Reflux Disease (GERD)

NCT00868296

TERMINATED Phase 3

Study Evaluating Desvenlafaxine Succinate Sustained-release (DVS SR) in Adult Outpatients With Pain Associated With Diabetic Peripheral Neuropathy

NCT00283842

COMPLETED Phase 1

Study Evaluating IMA-638 in Asthma

NCT00339872

COMPLETED Phase 3

Study Evaluating Desvenlafaxine Sustained-Release (DVS-SR) in Adult Outpatients With Major Depressive Disorder

NCT00277823

COMPLETED Phase 2

Study Evaluating SCA-136 in Subjects With Acute Exacerbations of Schizophrenia

NCT00265551

COMPLETED Phase 3

Study Evaluating Pantoprazole Sodium Enteric-Coated Spheroid Suspension In Infants With Presumed GERD

NCT00259012

TERMINATED Phase 2

Study Evaluating GAP-486 in Heart Rhythm

NCT00137293

TERMINATED Phase 2

Study Evaluating GAP-486 on Heart Rhythm in Patients With Coronary Artery Disease

NCT00137332

COMPLETED Phase 2

Study Evaluating Lecozotan SR in Mild to Moderate Alzheimer's Disease (AD)

NCT00151398

COMPLETED Phase 3

Study Evaluating Bazedoxifene/Conjugated Estrogen Combinations in Vasomotor Symptoms Associated With Menopause

NCT00238732

COMPLETED Phase 3

Study Evaluating Bazedoxifene/Conjugated Estrogen Combinations in Symptoms Associated With Menopause

NCT00234819

COMPLETED Phase 1

Study Comparing Premarin® Vaginal Cream Versus Premarin® Oral Tablets in Atrophic Vaginitis

NCT00167921

TERMINATED

Study Evaluating Metabolic Syndrome in Subjects Undergoing Gastric Bypass Bariatric Syndrome

NCT00283374

COMPLETED Phase 4

Study Comparing Tigecycline Versus Ceftriaxone Sodium Plus Metronidazole in Complicated Intra-abdominal Infection

NCT00195351

COMPLETED Phase 3

Study Evaluating Pantoprazole in Children With GERD

NCT00141817

COMPLETED Phase 2

Study Evaluating ERB-041 With Methotrexate in Rheumatoid Arthritis

NCT00141830

COMPLETED Phase 3

Study Evaluating Conjugated Estrogen Cream for Atrophic Vaginitis

NCT00137371

COMPLETED Phase 3

Study Evaluating Combination of Levonorgestrel (LNG) and Ethinyl Estradiol (EE) in Premenstrual Dysphoric Disorder

NCT00128934

COMPLETED Phase 4

Study Evaluating the Effect of Sirolimus on Non-Melanoma Skin Cancer in Kidney Transplant Recipients

NCT00129961

TERMINATED Phase 1

Study Evaluating TTI-237 in Advanced Malignant Solid Tumors.

NCT00195325

TERMINATED Phase 1

Study Evaluating Vaccine in Adults With HIV

NCT00195312

COMPLETED Phase 3

Study to Establish Bioequivalence of ReFacto AF (BDDrFVIII) With Advate (FLrFVIII) in Hemophilia A

NCT00141843

COMPLETED Phase 3

Study Evaluating Levonorgestrel/Ethinyl Estradiol (LNG/EE) in PMS

NCT00161681

TERMINATED Phase 2

Study Evaluating GAP-486 in Non-sustained Ventricular Tachycardia

NCT00124891

COMPLETED Phase 3

Study Evaluating Bifeprunox in Bipolar Depression

NCT00134459

COMPLETED Phase 3

Study Comparing a Pantoprazole Formulation to the Currently Marketed Tablet for GERD and Erosive Esophagitis

NCT00195208

COMPLETED Phase 3

Study Evaluating Bifeprunox in Bipolar Depression

NCT00245973

TERMINATED Phase 3

Study Comparing Sirolimus With Cyclosporine in a Calcineurin Inhibitor (CNI)-Free Regimen in Kidney Transplant Recipients

NCT00137345

COMPLETED Phase 2

Study Evaluating Etanercept in Moderate to Severe Asthma

NCT00141791

TERMINATED Phase 1

Study Evaluating TTI-237 in Advanced Malignant Solid Tumors

NCT00195247

COMPLETED

Study Evaluating Temsirolimus in Advanced Stage Squamous Cell Carcinoma of the Head & Neck

NCT00195299

COMPLETED Phase 2

Study Evaluating SRA-333 in Mild to Moderate Alzheimer's Disease (AD)

NCT00151333

COMPLETED

Study to Describe the Allergic Reactions to Factor IX in Patients With Hemophilia B

NCT00195221

COMPLETED Phase 1

Study Evaluating MYO-029 in Adult Muscular Dystrophy

NCT00104078

COMPLETED Phase 2

Study Evaluating ERB-041 in Endometriosis in Reproductive-Age Women

NCT00110487

COMPLETED Phase 1

Study Evaluating Vaccine in Adults With HIV

NCT00195234

COMPLETED Phase 1

Study Evaluating CMD-193 in Advanced Malignant Solid Tumors

NCT00161642

COMPLETED Phase 4

Study Comparing Etanercept and Methotrexate vs. Methotrexate Alone in Rheumatoid Arthritis

NCT00195494

COMPLETED Phase 1

Study Evaluating Pneumococcal Vaccine in Healthy Infants

NCT00205803

TERMINATED Phase 3

Study Evaluating CCI-779 and Letrozole in Post-menopausal Women With Breast Cancer

NCT00083993

COMPLETED NA

An Open Label Exploratory Study in Newly Diagnosed Prostate Cancer Patients

NCT00235794

COMPLETED Phase 3

Study Evaluating the Safety & Efficacy of DVS-223 SR for Relief of Vasomotor Symptoms Associated With Menopause

NCT00421031

COMPLETED Phase 3

Study Evaluating Tigecycline Versus Imipenem/Cilastatin in Hospital-Acquired Pneumonia

NCT00080496

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Phase Distribution

PhaseTrial count
Phase 1 74
Phase 2 28
Phase 3 43
Phase 4 10

What the Pipeline for Wyeth is now a wholly owned subsidiary of Pfizer Shows

According to the ClinicalTrials.gov registry, Wyeth is now a wholly owned subsidiary of Pfizer is linked to 167 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 139 are already marked complete, representing roughly 83% of the total.

The phase mix for Wyeth is now a wholly owned subsidiary of Pfizer reports 53 late-stage studies (Phase 3 and Phase 4 combined) and 102 earlier-phase studies (Phase 1 and Phase 2).

The top therapeutic focus area indexed for Wyeth is now a wholly owned subsidiary of Pfizer is Healthy with 5 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.