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
-
Pfizer Completes Acquisition of Therachon
-
Pfizer (PFE) Reports Positive Top-Line Results from Phase 4 Study of Crisaborole Ointment
-
Pfizer Announces Positive Top-Line Results from Phase 4 Study of Crisaborole Ointment, 2%, in Children Aged 3 Months to Less Than 24 Months with Mild to Moderate Atopic Dermatitis
-
Pfizer (PFE) Phase 3 Trial of Revatio in Newborns with PPHN Did Not Meet its Primary Efficacy Endpoint
-
Pfizer Announces Results from Phase 3 Trial of Revatio® (Sildenafil Citrate) in Newborns with Persistent Pulmonary Hypertension
-
Pfizer (PFE) Presents Initial Clinical Data on Phase 1b Gene Therapy Study for DMD
-
Pfizer Presents Initial Clinical Data on Phase 1b Gene Therapy Study for Duchenne Muscular Dystrophy (DMD)
-
Pfizer (PFE) Announces FDA Approval for Its Oncology Biosimilar, ZIRABEV
-
Pfizer Receives U.S. FDA Approval for Its Oncology Biosimilar, ZIRABEV™ (bevacizumab-bvzr)
-
Pfizer (PFE) Reports Election of Dr. Scott Gottlieb to Board
-
Scott Gottlieb Elected to Pfizer’s Board of Directors
-
Pfizer Declares Third-Quarter 2019 Dividend
-
Pfizer (PFE) Announce EC Approves TALZENNA for Patients with Inherited BRCA-Mutated Locally Advanced
-
European Commission Approves TALZENNA® (talazoparib) for Patients with Inherited (Germline) BRCA-Mutated Locally Advanced or Metastatic Breast Cancer
-
Pfizer to Acquire Array BioPharma
-
Pfizer (PFE) to Acquire Array BioPharma (ARRY) in $11.4 Billion Deal, $48/Share
-
Pfizer to Acquire Array BioPharma
-
Pfizer (PFE) Announces Results from XELJANZ XR ORAL Shift Study, The First Phase 3b/4 Study to Evaluate Methotrexate Withdrawal with JAK Inhibitor
-
Pfizer Announces Results from XELJANZ® XR (tofacitinib) ORAL Shift Study, The First Phase 3b/4 Study to Evaluate Methotrexate Withdrawal with a JAK Inhibitor
-
Jeff Settleman, Ph.D., Joins Pfizer to Lead Oncology Research & Development
-
Matinas BioPharma to Present at the 9th Annual LD Micro Invitational
-
Matinas BioPharma to Present at the 9th Annual LD Micro Invitational
-
Pfizer (PFE) Phase 3 Trial of LYRICA in PGTC Seizures Did Not Meet its Primary Endpoint
-
Pfizer Announces Top-Line Results from Phase 3 Trial of LYRICA® (pregabalin) in Primary Generalized Tonic-Clonic Seizures
-
Verily Forms Strategic Alliances with Novartis, Otsuka, Pfizer and Sanofi to Transform Clinical Research
-
Pfizer Oncology to Showcase New Data from Innovative Science That Address Patient Needs at ASCO 2019 Annual Meeting
-
Matinas BioPharma Announces a Research Collaboration with ViiV Healthcare to Evaluate Formulation of Antiviral Drug Candidates
-
Matinas BioPharma Announces a Research Collaboration with ViiV Healthcare to Evaluate Formulation of Antiviral Drug Candidates
-
Pfizer (PFE) Announces Positive Top-Line Results from Phase 3 Study of Investigational Oral JAK1 Candidate, Abrocitinib in Patients Aged 12 and Older with Moderate to Severe AD
-
Pfizer Announces Positive Top-Line Results from Phase 3 Study of Investigational Oral JAK1 Candidate, Abrocitinib (PF-04965842), in Patients Aged 12 and Older with Moderate to Severe Atopic Dermatitis
-
FDA Approves BAVENCIO® (avelumab) Plus INLYTA® (axitinib) Combination for Patients with Advanced Renal Cell Carcinoma
-
Pfizer (PFE) Acquires Therachon for $340M Upfront, $470M Contingent
-
Pfizer Acquires Clinical-Stage Biotech Therachon
-
Pfizer (PFE) Announces EC Approves LORVIQUA for Certain Adult Patients with Previously-Treated ALK-Positive Advanced NSCLC
-
European Commission Approves LORVIQUA® (lorlatinib) for Certain Adult Patients with Previously-Treated ALK-Positive Advanced Non-Small Cell Lung Cancer
-
Pfizer (PFE) Announces U.S. FDA Approves VYNDAQEL and VYNDAMAX for Use in Patients with Transthyretin Amyloid Cardiomyopathy
-
U.S. FDA Approves VYNDAQEL® and VYNDAMAX™ for Use in Patients with Transthyretin Amyloid Cardiomyopathy, a Rare and Fatal Disease
-
Pfizer (PFE) Receives Positive CHMP Opinion for TALZENNA
-
Pfizer Receives Positive CHMP Opinion for TALZENNA® (talazoparib) for Patients with Inherited (Germline) BRCA-Mutated Locally Advanced or Metastatic Breast Cancer
-
Pfizer Hosts Annual Meeting of Shareholders
-
Pfizer (PFE). Eli Lilly & Co. (NYSE:LLY) Report Top-Line Results From Long-Term Phase 3 Study of Tanezumab in Patients With Osteoarthritis
-
Pfizer and Lilly Announce Top-Line Results From Long-Term Phase 3 Study of Tanezumab in Patients With Osteoarthritis
-
Pfizer Invites Public to Listen to Webcast of April 25 Annual Meeting of Shareholders
-
Pfizer Announces Presentation of Data from a Phase 2 Study of its 20-Valent Pneumococcal Conjugate Vaccine Candidate Being Investigated for the Prevention of Invasive Disease and Pneumonia in Adults A
-
Pfizer (PFE) Announces FDA Approval of IBRANCE for Treatment of Men with HR+, HER2- Metastatic Breast Cancer
-
U.S. FDA Approves IBRANCE® (palbociclib) for the Treatment of Men with HR+, HER2- Metastatic Breast Cancer
-
Pfizer (PFE) Announces VIZIMPRO Receives MAA in EU for First-Line Treatment of Adult Patients with EGFR-Mutated NSCLC
-
VIZIMPRO® (dacomitinib) Receives Marketing Authorization in European Union (EU) for the First-Line Treatment of Adult Patients with EGFR-Mutated Non-Small Cell Lung Cancer
-
Sangamo Therapeutics (SGMO), Pfizer (PFE) Report Phase 1/2 Interim Data For Investigational Hemophilia A Gene Therapy
-
Sangamo and Pfizer Announce Phase 1/2 Interim Data for Investigational Hemophilia A Gene Therapy

