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 1 of 4

COMPLETED Phase 1

Study Comparing Two Different Tablet Formulations Of Bosutinib Under Fed Conditions

NCT01080365

COMPLETED NA

A Study To Evaluate Methods To Evaluate Back Pain

NCT01045993

COMPLETED NA

Study of Count Coughs in Subjects With Acute Upper Respiratory Tract Infections

NCT01062256

COMPLETED Phase 1

Study Evaluating The Potential Effect Of Lansoprazole On The Pharmacokinetics Of Bosutinib In Healthy Subjects

NCT00952913

COMPLETED Phase 1

Study Evaluating The Coadministration of Begacestat And Donepezil

NCT00959881

COMPLETED Phase 1

Study Comparing Two Different Tablet Formulations Of Bosutinib

NCT00934674

COMPLETED Phase 1

Study to Evaluate Whether BLI-489 Can be Safely Tolerated by Healthy Subjects Given Multiple Doses

NCT00909688

COMPLETED Phase 1

Study Evaluating The Effect of Bosutinib (SKI-606) On Cardiac Repolarization (Rhythms Of The Heart)

NCT00914121

COMPLETED Phase 1

Comparative Formulation Study of Vabicaserin

NCT00928551

COMPLETED Phase 1

Study Evaluating BLI-489 and Piperacillin in Healthy Subjects

NCT00894439

TERMINATED

Observational Study Analyzing RNA Expression Of Endometrial Biopsy Samples From Placebo, Bazedoxifene/Conjugated Estrogens And Raloxifene

NCT00847821

COMPLETED Phase 3

Study Evaluating Desvenlafaxine Succinate Sustained Release In Adults With Major Depressive Disorder

NCT00863798

COMPLETED Phase 1

Study Evaluating the Safety, Pharmacokinetics (PK), and Pharmacodynamices (PD) of HSD-016

NCT00838461

COMPLETED Phase 1

Multiple Dose Study Evaluating the Safety and Tolerability of NSA-789

NCT00795730

COMPLETED Phase 1

Study Evaluating Single Doses of BLI-489 in Healthy Subjects

NCT00820404

COMPLETED Phase 1

Study Evaluating Single Doses of ILV-095 in Healthy Subjects

NCT00822835

TERMINATED Phase 1

Study Evaluating HTC-867 in Healthy Young and Elderly Subjects

NCT00827489

COMPLETED Phase 1

Study Evaluating The Mass Balance And Metabolic Disposition Of SKI-606

NCT00757341

COMPLETED Phase 1

Study of the Safety, Tolerability, and Pharmacokinetics of GAP-134 Administered Intravenously

NCT00783341

COMPLETED Phase 4

Determine The Percentage Of Depressed Outpatients Who Do Not Effectively Metabolize Extended-release Venlafaxine HCl

NCT00788944

COMPLETED Phase 1

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

COMPLETED Phase 1

Study Evaluating Premarin and Bazedoxifene Potential Interaction

NCT00745173

COMPLETED Phase 1

Single Ascending Dose Study of the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of HSD-016

NCT00739232

COMPLETED Phase 1

Study Evaluating the Safety and Pharmacokinetics of Ascending Single IV Doses of ERB-257

NCT00722501

COMPLETED Phase 4

Study Comparing the Efficacy of Two Ibuprofen Formulations

NCT00740857

TERMINATED Phase 1

Study Evaluating PAZ-417 in Cerebrospinal Fluid in Subjects With Alzheimer's Disease

NCT00739037

COMPLETED Phase 1

Study Evaluating the Pharmacokinetics of Venlafaxine Extended-Release (ER) and Desvenlafaxine Succinate Sustained-Release (DVS SR) 50 mg in Healthy Subjects

NCT00727064

COMPLETED Phase 1

Study Evaluating Potential Drug Interaction Of Bazedoxifene & Premarin In Healthy Postmenopausal Women

NCT00706225

TERMINATED Phase 2

A Study Evaluating Desvenlafaxine Sustained Release (DVS SR) in Adult Female Outpatients With Fibromyalgia

NCT00696787

COMPLETED Phase 2

Study Evaluating Desvenlafaxine Succinate Sustained-Release Tablets (DVS SR) In The Treatment Of Child and Adolescent Outpatients With Major Depressive Disorder

NCT00669110

TERMINATED Phase 1

A Study of the Safety of PAZ-417 in Healthy Elderly Adults

NCT00663065

COMPLETED Phase 1

Study Evaluating the Safety and Tolerability of NSA-789

NCT00633048

COMPLETED Phase 1

Study GSI-136 in Healthy Young and Healthy Elderly Subjects

NCT00718731

COMPLETED Phase 2

Study Evaluating Desvenlafaxine Succinate Sustained-Release (DVS SR) In The Treatment Of Child And Adolescent Outpatients With Major Depressive Disorder

NCT00619619

COMPLETED Phase 1

Study Evaluating The Safety And Tolerability Of ILV-094 In Subjects With Psoriasis

NCT00563524

COMPLETED Phase 2

Study Evaluating the Pharmacokinetics (PK), Safety, and Tolerability of Tigecycline in Patients 8 to 11 Years of Age

NCT00488345

COMPLETED Phase 3

Study Evaluating The Safety, Tolerability And Immunogenicity Of A 13-Valent Pneumococcal Conjugate Vaccine (13vPnC)

NCT00546572

COMPLETED Phase 3

Study Evaluating the Safety, Tolerability and Immunogenicity of 13vPnC as a 2-Dose Regimen or With 23vPS

NCT00574548

COMPLETED Phase 1

Study Evaluating PRA-027 Multiple Ascending Doses In Cycling And Postmenopausal Women

NCT00543790

COMPLETED Phase 3

Study Evaluating the Efficacy of an Ibuprofen Effervescent Tablet in the Treatment of Post-Surgical Dental Pain

NCT00631111

COMPLETED Phase 1

Study Evaluating the Safety of FXR-450 in Healthy Subjects

NCT00499629

COMPLETED Phase 1

Study Comparing Premarin®/MPA, PREMPRO® and Provera® in Healthy Postmenopausal Women

NCT00543634

COMPLETED Phase 1

Single Ascending Dose Study of the Safety, Tolerability, and Pharmacokinetics of GAP-134 Administered Intravenously

NCT00510029

COMPLETED Phase 1

Study Evaluating IMA-026 in Healthy Subjects

NCT00517348

TERMINATED Phase 1

Study Evaluating TRU-015 in B-Cell Non-Hodgkin's Lymphoma

NCT00521638

COMPLETED Phase 1

Study Evaluating Multiple Doses Of GSI-953 Within The Elderly Population

NCT00547560

COMPLETED Phase 1

Study Comparing Bioavailability of Oral Formulations of Vabicaserin

NCT00541996

TERMINATED Phase 1

Study of TRU-015 in Subjects With Membranous Nephropathy Secondary to Systemic Lupus Erythematosus

NCT00479622

COMPLETED Phase 1

Study Evaluating 3 New Formulations of SKI-606 in Healthy Adult Subjects

NCT00499538

COMPLETED Phase 1

HCV-796 and Midazolam Drug Interaction Study in Healthy Subjects

NCT00410254

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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.