New York, United States · Est. 1849 · 88,000 employees
Global pharmaceutical and biotechnology corporation.
Pipeline Programs↗
Distinct drugs in development (Preclinical–Phase 3)
Indications↗
Distinct diseases across all programs
Clinical Trials↗
All sponsored trials (all statuses)
Orange Book Patents
Across 17 drugs with upcoming expirations
Pipeline
By Phase
100 drugs in development
By Therapeutic Area
top 6
R&D Momentum
100/100
Pipeline Velocity
88/100
Trial Completion Rate
82/100
Pipeline Concentration
15/100
Pipeline Freshness
73/100
Strategic Signals
Activity
Last 14 days
Real-World Characteristics and Treatment Patterns of Patients With Transthyretin Amyloid Cardiomyopathy (ATTR-CM): A Multi-Country, Non-Interventional, Disease Registry
A PHASE 3 RANDOMIZED WITHDRAWAL AND DOSE-UP TITRATION, MULTICENTER EXTENSION STUDY INVESTIGATING THE SAFETY, EFFICACY, AND TOLERABILITY OF RITLECITINIB IN ADULT AND ADOLESCENT PARTICIPANTS WITH NONSEGMENTAL VITILIGO
HYMPAVZI S.C. INJECTION 150 MG PEN SPECIAL INVESTIGATION
A PHASE 3 RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY TO INVESTIGATE THE EFFICACY AND SAFETY OF RITLECITINIB IN PEDIATRIC PARTICIPANTS 6 TO LESS THAN 12 YEARS OF AGE WITH SEVERE ALOPECIA AREATA
LORLATINIB (PF-06463922) CONTINUATION PROTOCOL: AN OPEN-LABEL, SINGLE-ARM CONTINUATION STUDY FOR PARTICIPANTS WITH ALK-POSITIVE OR ROS1-POSITIVE NON-SMALL CELL LUNG CANCER (NSCLC) CONTINUING FROM PFIZER SPONSORED LORLATINIB CLINICAL STUDIES
KOREAN POST-MARKETING SURVEILLANCE VYNDAMAX (REGISTERED) CAPSULES FOR THE TREATMENT OF TRANSTHYRETIN AMYLOID CARDIOMYOPATHY (ATTR-CM)
LITFULO® CAPSULES SPECIAL INVESTIGATION
A PHASE 2, OPEN-LABEL EXTENSION STUDY TO INVESTIGATE THE SAFETY AND EFFICACY OF PF-07868489 ADMINISTERED TO ADULT PARTICIPANTS WITH PULMONARY ARTERIAL HYPERTENSION
EFFECTIVENESS OF PNEUMOCOCCAL VACCINATION (PCV20) TO PREVENT ALL-CAUSE PNEUMONIA AND LOWER RESPIRATORY TRACT INFECTIONS AMONG ADULTS ≥19 YEARS OF AGE WITH AN INCREASED RISK OF PNEUMOCOCCAL DISEASE AT KAISER PERMANENTE SOUTHERN CALIFORNIA
RETROSPECTIVE COHORT STUDY OF PREGNANCY OUTCOMES IN WOMEN EXPOSED TO RIMEGEPANT DURING PREGNANCY
A PHASE 3, MULTI-CENTER, OPEN-LABEL EXTENSION STUDY TO INVESTIGATE THE LONG-TERM SAFETY, TOLERABILITY, AND EFFICACY OF DAZUKIBART IN PARTICIPANTS WITH IDIOPATHIC INFLAMMATORY MYOPATHIES (INCLUDING PARTICIPANTS WITH DERMATOMYOSITIS OR POLYMYOSITIS)
AN INTERVENTIONAL EFFICACY AND SAFETY, PHASE 3, RANDOMIZED, DOUBLE-BLIND, 3-ARM STUDY TO INVESTIGATE IBUZATRELVIR IN ADULTS WITH SYMPTOMATIC COVID-19 WHO ARE SEVERELY IMMUNOCOMPROMISED
Details
Company Overview
$160.0B
Mkt Cap
$59.6B
Revenue
$1.0B
Cash
Therapeutic Focus
Recent SEC Filings
PFIZER INC (PFE) (CIK 0000078003)
Pipeline
Regulatory
Acanya — XACIATO
Application NDA215650 (NDA)
TIVDAK — TIVDAK
Application BLA761208 (BLA)
Padcev — PADCEV
Application BLA761137
Padcev — PADCEV
Application BLA761137
Padcev — PADCEV
Application BLA761137
Padcev — PADCEV
Application BLA761137
Cibinqo — CIBINQO
Application NDA213871 (NDA)
Padcev — PADCEV
Application BLA761137
Padcev — PADCEV
Application BLA761137
Coxanto — COXANTO
Application NDA217927 (NDA)
Opzelura — LITFULO
Application NDA215830 (NDA)
Talzenna — TALZENNA
Application NDA211651 (NDA)
Padcev — PADCEV
Application BLA761137
Padcev — PADCEV
Application BLA761137
Padcev — PADCEV
Application BLA761137
Zavzpret — ZAVZPRET
Application NDA216386 (NDA)
Talzenna — TALZENNA
Application NDA217439 (NDA)
Padcev — PADCEV
Application BLA761137
Padcev — PADCEV
Application BLA761137
Padcev — PADCEV
Application BLA761137
PFIZER INC (PFE) (CIK 0000078003)
Accession: 001-03619
Data sources: ClinicalTrials.gov (NIH) · OpenFDA (FDA) · ChEMBL (EMBL-EBI) · Open Targets (EBI/Sanger) · MedlinePlus (NIH) · PubMed (NIH) · SEC EDGAR (SEC)