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 1 of 4
Study Comparing Two Different Tablet Formulations Of Bosutinib Under Fed Conditions
NCT01080365
A Study To Evaluate Methods To Evaluate Back Pain
NCT01045993
Study of Count Coughs in Subjects With Acute Upper Respiratory Tract Infections
NCT01062256
Study Evaluating The Potential Effect Of Lansoprazole On The Pharmacokinetics Of Bosutinib In Healthy Subjects
NCT00952913
Study Evaluating The Coadministration of Begacestat And Donepezil
NCT00959881
Study Comparing Two Different Tablet Formulations Of Bosutinib
NCT00934674
Study to Evaluate Whether BLI-489 Can be Safely Tolerated by Healthy Subjects Given Multiple Doses
NCT00909688
Study Evaluating The Effect of Bosutinib (SKI-606) On Cardiac Repolarization (Rhythms Of The Heart)
NCT00914121
Comparative Formulation Study of Vabicaserin
NCT00928551
Study Evaluating BLI-489 and Piperacillin in Healthy Subjects
NCT00894439
Observational Study Analyzing RNA Expression Of Endometrial Biopsy Samples From Placebo, Bazedoxifene/Conjugated Estrogens And Raloxifene
NCT00847821
Study Evaluating Desvenlafaxine Succinate Sustained Release In Adults With Major Depressive Disorder
NCT00863798
Study Evaluating the Safety, Pharmacokinetics (PK), and Pharmacodynamices (PD) of HSD-016
NCT00838461
Multiple Dose Study Evaluating the Safety and Tolerability of NSA-789
NCT00795730
Study Evaluating Single Doses of BLI-489 in Healthy Subjects
NCT00820404
Study Evaluating Single Doses of ILV-095 in Healthy Subjects
NCT00822835
Study Evaluating HTC-867 in Healthy Young and Elderly Subjects
NCT00827489
Study Evaluating The Mass Balance And Metabolic Disposition Of SKI-606
NCT00757341
Study of the Safety, Tolerability, and Pharmacokinetics of GAP-134 Administered Intravenously
NCT00783341
Determine The Percentage Of Depressed Outpatients Who Do Not Effectively Metabolize Extended-release Venlafaxine HCl
NCT00788944
Study to Determine the Effect of a High-Fat Meal on the Relative Bioavailability and Pharmacokinetics of a Single Dose of Bosutinib Administered Orally to Healthy Subjects
NCT00721474
Study Evaluating Premarin and Bazedoxifene Potential Interaction
NCT00745173
Single Ascending Dose Study of the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of HSD-016
NCT00739232
Study Evaluating the Safety and Pharmacokinetics of Ascending Single IV Doses of ERB-257
NCT00722501
Study Comparing the Efficacy of Two Ibuprofen Formulations
NCT00740857
Study Evaluating PAZ-417 in Cerebrospinal Fluid in Subjects With Alzheimer's Disease
NCT00739037
Study Evaluating the Pharmacokinetics of Venlafaxine Extended-Release (ER) and Desvenlafaxine Succinate Sustained-Release (DVS SR) 50 mg in Healthy Subjects
NCT00727064
Study Evaluating Potential Drug Interaction Of Bazedoxifene & Premarin In Healthy Postmenopausal Women
NCT00706225
A Study Evaluating Desvenlafaxine Sustained Release (DVS SR) in Adult Female Outpatients With Fibromyalgia
NCT00696787
Study Evaluating Desvenlafaxine Succinate Sustained-Release Tablets (DVS SR) In The Treatment Of Child and Adolescent Outpatients With Major Depressive Disorder
NCT00669110
A Study of the Safety of PAZ-417 in Healthy Elderly Adults
NCT00663065
Study Evaluating the Safety and Tolerability of NSA-789
NCT00633048
Study GSI-136 in Healthy Young and Healthy Elderly Subjects
NCT00718731
Study Evaluating Desvenlafaxine Succinate Sustained-Release (DVS SR) In The Treatment Of Child And Adolescent Outpatients With Major Depressive Disorder
NCT00619619
Study Evaluating The Safety And Tolerability Of ILV-094 In Subjects With Psoriasis
NCT00563524
Study Evaluating the Pharmacokinetics (PK), Safety, and Tolerability of Tigecycline in Patients 8 to 11 Years of Age
NCT00488345
Study Evaluating The Safety, Tolerability And Immunogenicity Of A 13-Valent Pneumococcal Conjugate Vaccine (13vPnC)
NCT00546572
Study Evaluating the Safety, Tolerability and Immunogenicity of 13vPnC as a 2-Dose Regimen or With 23vPS
NCT00574548
Study Evaluating PRA-027 Multiple Ascending Doses In Cycling And Postmenopausal Women
NCT00543790
Study Evaluating the Efficacy of an Ibuprofen Effervescent Tablet in the Treatment of Post-Surgical Dental Pain
NCT00631111
Study Evaluating the Safety of FXR-450 in Healthy Subjects
NCT00499629
Study Comparing Premarin®/MPA, PREMPRO® and Provera® in Healthy Postmenopausal Women
NCT00543634
Single Ascending Dose Study of the Safety, Tolerability, and Pharmacokinetics of GAP-134 Administered Intravenously
NCT00510029
Study Evaluating IMA-026 in Healthy Subjects
NCT00517348
Study Evaluating TRU-015 in B-Cell Non-Hodgkin's Lymphoma
NCT00521638
Study Evaluating Multiple Doses Of GSI-953 Within The Elderly Population
NCT00547560
Study Comparing Bioavailability of Oral Formulations of Vabicaserin
NCT00541996
Study of TRU-015 in Subjects With Membranous Nephropathy Secondary to Systemic Lupus Erythematosus
NCT00479622
Study Evaluating 3 New Formulations of SKI-606 in Healthy Adult Subjects
NCT00499538
HCV-796 and Midazolam Drug Interaction Study in Healthy Subjects
NCT00410254
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.