http://www.twitter.comTwitter is a service for friends, family, and co-workers to communicate and stay connected through the exchange of quick, frequent answers to one simple question: What are you doing?
View Older Stories View More Recent Stories
-
Akcea and Ionis Announce Closing of Licensing Agreement with Pfizer Inc. for Investigative Antisense Therapy AKCEA-ANGPTL3-L(Rx)
-
Pfizer (PFE) Reports FDA Approval of Biosimilar, ABRILADA (adalimumab-afzb) for Multiple Inflammatory Conditions
-
FDA Approves Pfizer’s Biosimilar, ABRILADA™ (adalimumab-afzb) for Multiple Inflammatory Conditions
-
Bristol-Myers Squibb and Pfizer Announce Randomized, Controlled Trial to Evaluate the Effect of Atrial Fibrillation Screening on Health Outcomes in Older Individuals
-
Mylan (MYL), Pfizer (PFE) Said New Company to Be Named 'Viatris'
-
Mylan and Pfizer Announce Viatris as the New Company Name in the Planned Mylan-Upjohn Combination
-
Mylan and Pfizer Announce Viatris as the New Company Name in the Planned Mylan-Upjohn Combination
-
Pfizer (PFE) Reports Results of Phase 3 Study for XELJANZ (tofacitinib) in Juvenile Idiopathic Arthritis
-
Pfizer Announces Results of Phase 3 Study for XELJANZ® (tofacitinib) in Juvenile Idiopathic Arthritis Ahead of Presentation at 2019 American College of Rheumatology/Association of Rheumatology Profes
-
EMD Serono, Pfizer (PFE) Provide Update on Phase III JAVELIN Gastric 100 Trial
-
EMD Serono and Pfizer Provide Update on Phase III JAVELIN Gastric 100 Trial
-
European Commission Approves BAVENCIO® (avelumab) Plus Axitinib Combination for First-Line Treatment of Patients With Advanced Renal Cell Carcinoma
-
OPKO Health (OPK), Pfizer (PFE) announced Phase 3 trial evaluating somatrogon dosed once-weekly in pre-pubertal children with GHD met its primary endpoint
-
OPKO and Pfizer Announce Positive Phase 3 Top-Line Results for Somatrogon, an Investigational Long-Acting Human Growth Hormone to Treat Children with Growth Hormone Deficiency
-
Pfizer (PFE) Reports Positive Phase 3 Data from Pivotal Study (JADE MONO-1)
-
Pfizer Presents Positive Phase 3 Data at the 28th Congress of the European Academy of Dermatology and Venereology for Abrocitinib in Moderate to Severe Atopic Dermatitis
-
Akcea Therapeutics (AKCA), Pfizer (PFE) Announce Licensing Agreement for investigative antisense therapy AKCEA-ANGPTL3-L(Rx)
-
Akcea and Pfizer Inc. Announce Licensing Agreement for investigative antisense therapy AKCEA-ANGPTL3-L(Rx)
-
Akcea and Pfizer Inc. Announce Licensing Agreement for investigative antisense therapy AKCEA-ANGPTL3-L(Rx)
-
Transgene Reports First Promising Efficacy Results with TG4001 in Combination with Avelumab in HPV-Positive Cancer at ESMO 2019
-
Pfizer (PFE) Presents Interim Analysis Results from Phase 3 BEACON CRC Trial of BRAFTOVI, MEKTOVI and Cetuximab for Treatment of BRAFV600E-mCRC
-
Pfizer Presents Interim Analysis Results from Phase 3 BEACON CRC Trial of BRAFTOVI® (Encorafenib), MEKTOVI® (Binimetinib) and Cetuximab for the Treatment of BRAFV600E-Mutant Metastatic Colorectal Ca
-
Pfizer Inc. Awards “Golden Tickets” to Neutrolis and Mediar Therapeutics
-
Pfizer (PFE) Announces Ian Read to Retire as Executive Chairman; CEO Dr. Albert Bourla Named Chairman
-
Ian Read to Retire as Executive Chairman of Pfizer’s Board of Directors; Chief Executive Officer Dr. Albert Bourla Named Chairman
-
Pfizer (PFE) Reports Positive Top-Line Results from Second Pivotal Phase 3 Study of Abrocitinib in Patients Aged 12 and Older with Moderate to Severe AD
-
Pfizer Announces Positive Top-Line Results from Second Pivotal Phase 3 Study of Investigational Oral JAK1 Candidate, Abrocitinib, in Patients Aged 12 and Older with Moderate to Severe Atopic Dermatiti
-
New Data for BAVENCIO® (avelumab) for Advanced Cancers to Be Presented at ESMO 2019
-
Pfizer Declares Fourth-Quarter 2019 Dividend
-
Pfizer (PFE) Presents New Evidence of IBRANCE Effectiveness in HR+, HER2- Metastatic Breast Cancer Patients
-
Pfizer Presents New Evidence of IBRANCE® (palbociclib) Effectiveness in HR+, HER2- Metastatic Breast Cancer Patients in Four Real-World Studies at ESMO Congress 2019
-
Merck KGaA, Pfizer (PFE) Announce CHMP Adopts Positive Opinion for BAVENCIO Plus Axitinib for First-Line Treatment of Patients with Advanced RCC
-
CHMP Adopts Positive Opinion for BAVENCIO® (avelumab) Plus Axitinib for First-Line Treatment of Patients with Advanced Renal Cell Carcinoma
-
Pfizer (PFE) Presents Scientific Advancements in Cancer Care at ESMO
-
Pfizer Presents Scientific Advancements in Cancer Care at the ESMO Congress 2019 Highlighting Expanded Portfolio
-
Pfizer (PFE) Announces Prelim. Results from Proof-of-Concept Phase 2 Study of 20-Valent Pneumococcal Conjugate Vaccine Candidate
-
Pfizer Announces Positive Preliminary Results from a Proof-of-Concept Phase 2 Study (B7471003) of its 20-Valent Pneumococcal Conjugate Vaccine Candidate Being Investigated for the Prevention of Invasi
-
Pfizer Invests Half Billion Dollars to Advance State-of-the-Art Gene Therapy Facility in Sanford, North Carolina
-
Pfizer Announces Phase 3 Top-Line Results for Rivipansel in Patients with Sickle Cell Disease Experiencing a Vaso-Occlusive Crisis
-
Pfizer Announces Closing of Joint Venture With GlaxoSmithKline to Create a Premier Global Consumer Healthcare Company
-
Pfizer (PFE) Completes Acquisition of Array Biopharma (ARRY)
-
Pfizer Completes Acquisition of Array Biopharma
-
Mylan (MYL) and Pfizer's (PFE) Upjohn to Combine
-
Mylan and Upjohn, a Division of Pfizer, to Combine, Creating a New Champion for Global Health Uniquely Positioned to Fulfill the World’s Need for Medicine
-
Mylan and Upjohn, a Division of Pfizer, to Combine, Creating a New Champion for Global Health Uniquely Positioned to Fulfill the World's Need for Medicine
-
Pfizer (PFE) Reports FDA Approval of RUXIENCE (rituximab-pvvr), a Biosimilar for Certain Cancers and Autoimmune Conditions
-
FDA Approves Pfizer’s Biosimilar, RUXIENCE™ (rituximab-pvvr), for Certain Cancers and Autoimmune Conditions
-
Hong Kong Sports and Leisure Expo opens today
-
Sangamo Therapeutics (SGMO), Pfizer (PFE) Report Updated Phase 1/2 Results for SB-525 Investigational Hemophilia A Gene Therapy
-
Sangamo and Pfizer Announce Updated Phase 1/2 Results for SB-525 Investigational Hemophilia A Gene Therapy Showing Sustained Increased Factor VIII Levels

