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 2 of 4

COMPLETED Phase 1

Study Evaluating the Pharmacokinetics of the Potential Drug Interaction Between HCV-796 and Desipramine

NCT00500721

COMPLETED Phase 2

Study Evaluating the Safety,Tolerability, PK and PD of SAM-531 in the Subjects With Mild to Moderate Alzheimer's Disease

NCT00481520

COMPLETED Phase 3

Study Evaluating 13-valent Pneumococcal Conjugate Vaccine In Healthy Infants

NCT00444457

COMPLETED Phase 1

Study Evaluating AGG-523 in Subjects With Severe Osteoarthritis Requiring Total Knee Replacement

NCT00454298

COMPLETED Phase 4

Benzocaine Gel Toothache Dose-Response Study

NCT00474175

COMPLETED Phase 1

Bioequivalence Study of 3 New Formulations of Premarin/MPA Compared With Premarin/MPA (Prempro)

NCT00472927

COMPLETED Phase 1

Study Evaluating GSI-953 in Healthy Young and Alzheimer's Patients

NCT00479219

COMPLETED Phase 1

Study Of Pharmacokinetic (PK) Profile of Bazedoxifene (BZA) in 2 BZA/Conjugated Estrogen Forms

NCT00479778

COMPLETED Phase 1

Study Evaluating the Safety and Tolerability of SCA-136 in Healthy Japanese and Non-Japanese Female Subjects

NCT00458107

COMPLETED Phase 1

Study Evaluating Bazedoxifene/Conjugated Estrogens Combinations in Fed and Fasting in Healthy, Postmenopausal Women

NCT00465075

COMPLETED Phase 1

Study Evaluating Drug Interaction Between Multiple Doses of Ketoconazole and a Single Dose of SKI-606

NCT00434486

TERMINATED Phase 1

A Study Combining Treatment With Temsirolimus and Sunitinib for Subjects With Advanced Renal Cell Carcinoma

NCT00417677

COMPLETED Phase 1

Study Evalutating the Pharmacokinetics (PK) and Safety of a Single Dose of Desvenlafaxine Sustained Release (DVS SR)

NCT00440427

COMPLETED Phase 1

Study Evaluating AGG-523 in Subjects With Osteoarthritis

NCT00427687

COMPLETED Phase 1

Study of the Safety, Tolerability, and PK of PRA-027 Administered to Women of Nonchildbearing Potential

NCT00427544

COMPLETED Phase 2

A Study of rhBMP-2/CPM in Closed Fractures of the Humerus

NCT00384852

COMPLETED Phase 1

Study Evaluating Single Doses of PPM-204 on the Electrical Pathways of the Heart

NCT00447629

COMPLETED Phase 3

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

TERMINATED Phase 2

Study Evaluating PPM-204 In Subjects With Type 2 Diabetes

NCT00425919

TERMINATED Phase 3

Study Evaluating Bifeprunox in Patients With Schizophrenia.

NCT00366327

COMPLETED Phase 1

Study of the Safety, Tolerability, Pharmacokinetics and Pharmcodynamics of ILV-094 in Healthy Subjects

NCT00447681

COMPLETED Phase 1

Study To Evaluate The Pharmacokinetic Interaction Between PLA-695 And Methotrexate In Adults With Rheumatoid Arthritis

NCT00440492

COMPLETED Phase 1

Pharmacokinetic Study Of Tigecycline In Adult Subjects With Primary Biliary Cirrhosis

NCT00406237

COMPLETED Phase 3

Study Evaluating Desvenlafaxine Succinate Sustained Release (DVS SR) vs. Escitalopram in Postmenopausal Women

NCT00406640

COMPLETED Phase 2

Feasibility And Safety Study Of rhBMP-2/CPM For Hip Fractures

NCT00384358

TERMINATED Phase 1

Study Evaluating SCA-136 Tolerability With Dose Titration and Food

NCT00420706

COMPLETED Phase 1

Study to Evaluate the Effects of Age & Gender on PK, Safety & Tolerability of HCV-796 Administered to Healthy Subjects

NCT00407173

COMPLETED Phase 3

Open Label Extension Study of Bifeprunox

NCT00366171

TERMINATED Phase 2

A Phase 2/3 Multicenter, Controlled Trial Of rhBMP-2/CPM In Tibial Fractures

NCT00387686

TERMINATED Phase 2

A Study Comparing 4 Dose Regimens of PLA-695, Naproxen, and Placebo In Subjects With Osteoarthritis Of The Knee

NCT00396955

TERMINATED Phase 3

Study Comparing Bifeprunox to Risperidone in Treatment of Outpatients With Schizophrenia With Weight as Primary Endpoint

NCT00366704

COMPLETED Phase 2

A Study Evaluating the Safety and Clinical Activity of HCV-796 in Treatment-Naive and Non-Responder Subjects

NCT00367887

COMPLETED

Effect of Bazedoxifene, Raloxifene, and Placebo on Breast Density

NCT00418236

COMPLETED Phase 4

Study Comparing the Safety and Efficacy of Tigecycline With Ampicillin-Sulbactam or Amoxicillin-Clavulanate to Treat Skin Infections

NCT00368537

COMPLETED Phase 3

Study Evaluating Desvenlafaxine Succinate Sustained Release (DVS SR) Versus Placebo in Peri- and Postmenopausal Women

NCT00369343

COMPLETED Phase 4

Study Of The Safety And Efficacy Of Conversion From A CNI To Sirolimus In Renally-Impaired Heart Transplant Recipients

NCT00369382

COMPLETED Phase 3

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

NCT00366652

COMPLETED Phase 1

Study Evaluating the Pharmacokinetics of Tigecycline in Human Bone

NCT00376324

COMPLETED Phase 3

Study Evaluating the Efficacy and Safety of Pantoprazole in Infants With Symptomatic Gastroesophageal Reflux Disease (GERD)

NCT00365300

COMPLETED Phase 1

Study Evaluating LXR-623 in Healthy Subjects

NCT00366522

TERMINATED Phase 2

Study Evaluating the Efficacy of DVS-233 in Fibromyalgia

NCT00301431

COMPLETED Phase 3

Study Comparing the Affect of Bifeprunox Vs Olanzapine on Weight During the Treatment of Outpatients With Schizophrenia.

NCT00380224

COMPLETED

Study Evaluating PAZ-417 in Healthy Young/Elderly

NCT00366288

COMPLETED Phase 3

Study Evaluating Pantoprazole in Neonates and Preterm Infants With GERD

NCT00362609

COMPLETED Phase 1

Study Evaluating the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Multiple Ascending Doses in Healthy

NCT00380900

COMPLETED Phase 3

Study of the Safety and Efficacy of Desvenlafaxine Succinate for Vasomotor Symptoms in Postmenopausal Women

NCT00369434

COMPLETED Phase 1

Study Evaluating the Gastrointestinal Safety of PLA-695 Compared to Placebo and Naproxen

NCT00366262

COMPLETED Phase 1

Study Evaluating IMA-638 in Healthy Japanese

NCT00340327

COMPLETED Phase 4

Open-Label, Randomized Study Evaluating Treatment With Venlafaxine Extended-Release Plus Dialogues Time to Talk Program

NCT00401726

COMPLETED Phase 1

Study Comparing Two Manufacturing Processes for Levonorgestrel 90 mg/Ethinyl Estradiol 20 mg (LNG/EE) in Healthy, Cycling Women

NCT00319163

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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.