Wyeth is now a wholly owned subsidiary of Pfizer
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
Study Evaluating Pantoprazole in Children With Gastroesophageal Reflux Disease (GERD)
NCT00300755
Study Evaluating the Safety of HCV-796 in Subjects With Liver Disease and in Healthy Adults
NCT00314054
Study Evaluating the Pharmacokinetics of Venlafaxine ER and Desvenlafaxine SR in Healthy Subjects
NCT00329186
Study Evaluating the Effects of Multiple Oral Doses of ERB-041 on Cardiac Repolarization in Healthy Subjects
NCT00316459
Study Evaluating the Effects of DVS SR and Paroxetine on the Pharmacokinetics of Desipramine in Healthy Subjects
NCT00329147
Study Evaluating the Safety and Efficacy of ERB-041 on Reduction of Symptoms Associated With Endometriosis in Reproductive-Aged Women
NCT00318500
Study Evaluating B-Domain Deleted Recombinant Factor VIII (BDDrFVIII, ReFacto AF) in Patients With Hemophilia A Undergoing Elective Major Surgery
NCT00243659
Open Label Safety Study of Enteric-Coated Spheroid Suspension in Infants Aged Less Than 12 Months With Presumed Gastroesophageal Reflux Disease (GERD)
NCT00868296
Study Evaluating Desvenlafaxine Succinate Sustained-release (DVS SR) in Adult Outpatients With Pain Associated With Diabetic Peripheral Neuropathy
NCT00283842
Study Evaluating IMA-638 in Asthma
NCT00339872
Study Evaluating Desvenlafaxine Sustained-Release (DVS-SR) in Adult Outpatients With Major Depressive Disorder
NCT00277823
Study Evaluating SCA-136 in Subjects With Acute Exacerbations of Schizophrenia
NCT00265551
Study Evaluating Pantoprazole Sodium Enteric-Coated Spheroid Suspension In Infants With Presumed GERD
NCT00259012
Study Evaluating GAP-486 in Heart Rhythm
NCT00137293
Study Evaluating GAP-486 on Heart Rhythm in Patients With Coronary Artery Disease
NCT00137332
Study Evaluating Lecozotan SR in Mild to Moderate Alzheimer's Disease (AD)
NCT00151398
Study Evaluating Bazedoxifene/Conjugated Estrogen Combinations in Vasomotor Symptoms Associated With Menopause
NCT00238732
Study Evaluating Bazedoxifene/Conjugated Estrogen Combinations in Symptoms Associated With Menopause
NCT00234819
Study Comparing Premarin® Vaginal Cream Versus Premarin® Oral Tablets in Atrophic Vaginitis
NCT00167921
Study Evaluating Metabolic Syndrome in Subjects Undergoing Gastric Bypass Bariatric Syndrome
NCT00283374
Study Comparing Tigecycline Versus Ceftriaxone Sodium Plus Metronidazole in Complicated Intra-abdominal Infection
NCT00195351
Study Evaluating Pantoprazole in Children With GERD
NCT00141817
Study Evaluating ERB-041 With Methotrexate in Rheumatoid Arthritis
NCT00141830
Study Evaluating Conjugated Estrogen Cream for Atrophic Vaginitis
NCT00137371
Study Evaluating Combination of Levonorgestrel (LNG) and Ethinyl Estradiol (EE) in Premenstrual Dysphoric Disorder
NCT00128934
Study Evaluating the Effect of Sirolimus on Non-Melanoma Skin Cancer in Kidney Transplant Recipients
NCT00129961
Study Evaluating TTI-237 in Advanced Malignant Solid Tumors.
NCT00195325
Study Evaluating Vaccine in Adults With HIV
NCT00195312
Study to Establish Bioequivalence of ReFacto AF (BDDrFVIII) With Advate (FLrFVIII) in Hemophilia A
NCT00141843
Study Evaluating Levonorgestrel/Ethinyl Estradiol (LNG/EE) in PMS
NCT00161681
Study Evaluating GAP-486 in Non-sustained Ventricular Tachycardia
NCT00124891
Study Evaluating Bifeprunox in Bipolar Depression
NCT00134459
Study Comparing a Pantoprazole Formulation to the Currently Marketed Tablet for GERD and Erosive Esophagitis
NCT00195208
Study Evaluating Bifeprunox in Bipolar Depression
NCT00245973
Study Comparing Sirolimus With Cyclosporine in a Calcineurin Inhibitor (CNI)-Free Regimen in Kidney Transplant Recipients
NCT00137345
Study Evaluating Etanercept in Moderate to Severe Asthma
NCT00141791
Study Evaluating TTI-237 in Advanced Malignant Solid Tumors
NCT00195247
Study Evaluating Temsirolimus in Advanced Stage Squamous Cell Carcinoma of the Head & Neck
NCT00195299
Study Evaluating SRA-333 in Mild to Moderate Alzheimer's Disease (AD)
NCT00151333
Study to Describe the Allergic Reactions to Factor IX in Patients With Hemophilia B
NCT00195221
Study Evaluating MYO-029 in Adult Muscular Dystrophy
NCT00104078
Study Evaluating ERB-041 in Endometriosis in Reproductive-Age Women
NCT00110487
Study Evaluating Vaccine in Adults With HIV
NCT00195234
Study Evaluating CMD-193 in Advanced Malignant Solid Tumors
NCT00161642
Study Comparing Etanercept and Methotrexate vs. Methotrexate Alone in Rheumatoid Arthritis
NCT00195494
Study Evaluating Pneumococcal Vaccine in Healthy Infants
NCT00205803
Study Evaluating CCI-779 and Letrozole in Post-menopausal Women With Breast Cancer
NCT00083993
An Open Label Exploratory Study in Newly Diagnosed Prostate Cancer Patients
NCT00235794
Study Evaluating the Safety & Efficacy of DVS-223 SR for Relief of Vasomotor Symptoms Associated With Menopause
NCT00421031
Study Evaluating Tigecycline Versus Imipenem/Cilastatin in Hospital-Acquired Pneumonia
NCT00080496
Phase Distribution
| Phase | Trial count |
|---|---|
| Phase 1 | 74 |
| Phase 2 | 28 |
| Phase 3 | 43 |
| Phase 4 | 10 |
Therapeutic Areas
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.
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.