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 2 of 4
Study Evaluating the Pharmacokinetics of the Potential Drug Interaction Between HCV-796 and Desipramine
NCT00500721
Study Evaluating the Safety,Tolerability, PK and PD of SAM-531 in the Subjects With Mild to Moderate Alzheimer's Disease
NCT00481520
Study Evaluating 13-valent Pneumococcal Conjugate Vaccine In Healthy Infants
NCT00444457
Study Evaluating AGG-523 in Subjects With Severe Osteoarthritis Requiring Total Knee Replacement
NCT00454298
Benzocaine Gel Toothache Dose-Response Study
NCT00474175
Bioequivalence Study of 3 New Formulations of Premarin/MPA Compared With Premarin/MPA (Prempro)
NCT00472927
Study Evaluating GSI-953 in Healthy Young and Alzheimer's Patients
NCT00479219
Study Of Pharmacokinetic (PK) Profile of Bazedoxifene (BZA) in 2 BZA/Conjugated Estrogen Forms
NCT00479778
Study Evaluating the Safety and Tolerability of SCA-136 in Healthy Japanese and Non-Japanese Female Subjects
NCT00458107
Study Evaluating Bazedoxifene/Conjugated Estrogens Combinations in Fed and Fasting in Healthy, Postmenopausal Women
NCT00465075
Study Evaluating Drug Interaction Between Multiple Doses of Ketoconazole and a Single Dose of SKI-606
NCT00434486
A Study Combining Treatment With Temsirolimus and Sunitinib for Subjects With Advanced Renal Cell Carcinoma
NCT00417677
Study Evalutating the Pharmacokinetics (PK) and Safety of a Single Dose of Desvenlafaxine Sustained Release (DVS SR)
NCT00440427
Study Evaluating AGG-523 in Subjects With Osteoarthritis
NCT00427687
Study of the Safety, Tolerability, and PK of PRA-027 Administered to Women of Nonchildbearing Potential
NCT00427544
A Study of rhBMP-2/CPM in Closed Fractures of the Humerus
NCT00384852
Study Evaluating Single Doses of PPM-204 on the Electrical Pathways of the Heart
NCT00447629
Study Evaluating the Safety and Efficacy of a Once-daily Dose of Tigecycline vs Ertapenem in Diabetic Foot Infections (DFI) With a Substudy in Patients With Diabetic Foot Infections Complicated by Osteomyelitis.
NCT00366249
Study Evaluating PPM-204 In Subjects With Type 2 Diabetes
NCT00425919
Study Evaluating Bifeprunox in Patients With Schizophrenia.
NCT00366327
Study of the Safety, Tolerability, Pharmacokinetics and Pharmcodynamics of ILV-094 in Healthy Subjects
NCT00447681
Study To Evaluate The Pharmacokinetic Interaction Between PLA-695 And Methotrexate In Adults With Rheumatoid Arthritis
NCT00440492
Pharmacokinetic Study Of Tigecycline In Adult Subjects With Primary Biliary Cirrhosis
NCT00406237
Study Evaluating Desvenlafaxine Succinate Sustained Release (DVS SR) vs. Escitalopram in Postmenopausal Women
NCT00406640
Feasibility And Safety Study Of rhBMP-2/CPM For Hip Fractures
NCT00384358
Study Evaluating SCA-136 Tolerability With Dose Titration and Food
NCT00420706
Study to Evaluate the Effects of Age & Gender on PK, Safety & Tolerability of HCV-796 Administered to Healthy Subjects
NCT00407173
Open Label Extension Study of Bifeprunox
NCT00366171
A Phase 2/3 Multicenter, Controlled Trial Of rhBMP-2/CPM In Tibial Fractures
NCT00387686
A Study Comparing 4 Dose Regimens of PLA-695, Naproxen, and Placebo In Subjects With Osteoarthritis Of The Knee
NCT00396955
Study Comparing Bifeprunox to Risperidone in Treatment of Outpatients With Schizophrenia With Weight as Primary Endpoint
NCT00366704
A Study Evaluating the Safety and Clinical Activity of HCV-796 in Treatment-Naive and Non-Responder Subjects
NCT00367887
Effect of Bazedoxifene, Raloxifene, and Placebo on Breast Density
NCT00418236
Study Comparing the Safety and Efficacy of Tigecycline With Ampicillin-Sulbactam or Amoxicillin-Clavulanate to Treat Skin Infections
NCT00368537
Study Evaluating Desvenlafaxine Succinate Sustained Release (DVS SR) Versus Placebo in Peri- and Postmenopausal Women
NCT00369343
Study Of The Safety And Efficacy Of Conversion From A CNI To Sirolimus In Renally-Impaired Heart Transplant Recipients
NCT00369382
Study Evaluating the Effects of DVS SR and Duloxetine on the Pharmacokinetics of Desipramine in Healthy Subjects
NCT00366652
Study Evaluating the Pharmacokinetics of Tigecycline in Human Bone
NCT00376324
Study Evaluating the Efficacy and Safety of Pantoprazole in Infants With Symptomatic Gastroesophageal Reflux Disease (GERD)
NCT00365300
Study Evaluating LXR-623 in Healthy Subjects
NCT00366522
Study Evaluating the Efficacy of DVS-233 in Fibromyalgia
NCT00301431
Study Comparing the Affect of Bifeprunox Vs Olanzapine on Weight During the Treatment of Outpatients With Schizophrenia.
NCT00380224
Study Evaluating PAZ-417 in Healthy Young/Elderly
NCT00366288
Study Evaluating Pantoprazole in Neonates and Preterm Infants With GERD
NCT00362609
Study Evaluating the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Multiple Ascending Doses in Healthy
NCT00380900
Study of the Safety and Efficacy of Desvenlafaxine Succinate for Vasomotor Symptoms in Postmenopausal Women
NCT00369434
Study Evaluating the Gastrointestinal Safety of PLA-695 Compared to Placebo and Naproxen
NCT00366262
Study Evaluating IMA-638 in Healthy Japanese
NCT00340327
Open-Label, Randomized Study Evaluating Treatment With Venlafaxine Extended-Release Plus Dialogues Time to Talk Program
NCT00401726
Study Comparing Two Manufacturing Processes for Levonorgestrel 90 mg/Ethinyl Estradiol 20 mg (LNG/EE) in Healthy, Cycling Women
NCT00319163
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.