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
-
AbbVie (ABBV) Announces Additional Data on IMBRUVICA Phase 3 in CLL/SLL
-
AbbVie Builds Upon Robust Body of IMBRUVICA® (ibrutinib) Data with Phase 3 Longer-Term Studies in Patients with Chronic Lymphocytic Leukemia and Small Lymphocytic Lymphoma Presented at the American S
-
AbbVie (ABBV) Issues Positive Update on Rova-T as r/r SCLC Treatment
-
AbbVie (ABBV) Announces Positive ABT-414 Phase 1 Data in Aggressive Brain Cancer
-
AbbVie Presents Encouraging Phase 1 Data for Investigational Medicine ABT-414 as Monotherapy in Patients with an Aggressive Brain Cancer at the 2016 American Society of Clinical Oncology Annual Meetin
-
Results of Phase 1a/1b Study of AbbVie's Investigational Medicine Rovalpituzumab Tesirine (Rova-T) Showed Overall Response Rate of 39 Percent in Pretreated Patients with Biomarker-Defined Small Cell L
-
AbbVie (ABBV) Plans Pipeline Update at R&D Day Event; Includes IMBRUVICA, ABT-484 Data
-
AbbVie to Highlight its Innovative Pipeline to the Investment Community
-
AbbVie's Research and Commitment to Helping People Living with Rheumatologic Diseases Highlighted at the Annual European Congress of Rheumatology (EULAR 2016)
-
AbbVie to Present at the Goldman Sachs 37th Annual Global Healthcare Conference
-
Biogen (BIIB), AbbVie (ABBV) Granted FDA Approval of ZINBRYTA for MS
-
AbbVie (ABBV) Receives EC Approval of IMBRUVICA as CLL Treatment
-
European Commission Approves IMBRUVICA® (ibrutinib) for First-Line Treatment of Patients with Chronic Lymphocytic Leukemia
-
Biogen and AbbVie Receive FDA Approval of Once-Monthly ZINBRYTA™ (Daclizumab) for Multiple Sclerosis
-
Biogen and AbbVie Receive FDA Approval of Once-Monthly ZINBRYTA™ (daclizumab) for Multiple Sclerosis
-
Biogen and AbbVie Receive FDA Approval of Once-Monthly ZINBRYTA™ (Daclizumab) for Multiple Sclerosis
-
CHMP Issues Positive Opinion on AbbVie's (ABBV) HUMIRA as non-Infectious Uveitis Treatment
-
AbbVie's HUMIRA® (adalimumab) Receives CHMP Positive Opinion to Treat Certain Forms of Non-Infectious Uveitis, a Disease that Can Severely Impact Vision[1]
-
AbbVie to Present at the Jefferies 2016 Healthcare Conference
-
IL-23 Inhibitor Risankizumab Induces Remission in Phase II Study in Patients with Moderate-to-Severe Crohn's Disease
-
AbbVie's Leadership in Gastroenterology Showcased at Digestive Disease Week® with New HUMIRA® (adalimumab) Long-Term, Real-World Research and Promising Anti-IL-23 Antibody Late-Breaking Data
-
AbbVie (ABBV) Announces Multiple Abstracts Evaluating Eight Medicines Across Cancer Types Presented at ASCO
-
AbbVie Demonstrates Progress in Oncology Research at ASCO 2016 Annual Meeting with Multiple Abstracts Evaluating Eight Medicines Across Cancer Types
-
AbbVie to Present at the UBS Global Health Care Conference
-
Bristol-Myers Squibb (BMY), AbbVie (ABBV) Announce EC Approval of Empliciti Combo as Multiple Myeloma Treatment
-
Bristol-Myers Squibb and AbbVie Announce European Commission Approval of Empliciti™ (elotuzumab) for the Treatment of Multiple Myeloma in Adult Patients Who Have Received at Least One Prior Therapy
-
AbbVie (ABBV) Announces FDA Update to IMBRUVICA Prescribing Info; Incldues Phase 3 Data for CLL
-
U.S. FDA Expands IMBRUVICA® (ibrutinib) Label to Include Overall Survival Data in Previously Untreated Chronic Lymphocytic Leukemia (CLL) and New Indication for Small Lymphocytic Lymphoma (SLL) Patie
-
European Medicines Agency Issues Positive Opinion for the Use of IMBRUVICA® (ibrutinib) as a First-Line Treatment for Chronic Lymphocytic Leukemia Patients
-
AbbVie to Present at the Bank of America Merrill Lynch 2016 Global Health Care Conference
-
Biogen (BIIB), AbbVie (ABBV) Receive Positive CHMP Opinion on ZINBRYTA in MS
-
Biogen and AbbVie Receive Positive Opinion from the CHMP on ZINBRYTA™ (Daclizumab) for Treatment of Multiple Sclerosis
-
AbbVie (ABBV) to Acquire Stemcentrx in ~$5.8B Cash and Stock Deal
-
AbbVie Reports First-Quarter 2016 Financial Results
-
AbbVie to Expand Oncology Presence Through Acquisition of Stemcentrx and its Novel, Late-Stage Rova-T Compound for Small Cell Lung Cancer
-
AbbVie (ABBV) Receives FDA Approval of Viekira Pak sNDA for Use Without RBV
-
AbbVie Receives U.S. FDA Approval of Supplemental New Drug Application for VIEKIRA PAK® (ombitasvir, paritaprevir, and ritonavir tablets; dasabuvir tablets) without Ribavirin in Genotype 1b Chronic H
-
CytomX (CTMX), AbbVie (ABBV) Enter Collaboration to Develop Probody Drug Conjugates Against CD71
-
AbbVie and CytomX Announce Strategic Collaboration for Probody Drug Conjugates
-
CytomX and AbbVie Announce Strategic Collaboration for Probody Drug Conjugates
-
AbbVie (ABBV), argenx Enter Collaboration on ARGX-115 Against Novel Immuno-Oncology Target
-
AbbVie and argenx to Collaborate on ARGX-115 Against Novel Immuno-Oncology Target
-
argenx and AbbVie to Collaborate on ARGX-115 Against Novel Immuno-Oncology Target
-
AbbVie (ABBV), University of Chicago Enter Cancer Research Collaboration
-
AbbVie, University of Chicago collaborate to advance cancer research
-
Biogen (BIIB), AbbVie (ABBV) Present Data at AAN Highlighting Impact of ZINBRYTA on Cognitive Outcomes and Targeted MOA
-
Data Presented at AAN Highlight Impact of ZINBRYTA™ (Daclizumab HYP) on Cognitive Outcomes and the Reversibility of Its Targeted Mechanism of Action
-
AbbVie to Present at the Deutsche Bank 41st Annual Health Care Conference
-
AbbVie (ABBV) Announces Positive Data from ABT-493, ABT-530 Phase 2 in HCV Genotypes 1 - 6 (ENTA)
-
AbbVie Presents New Phase 2 Data for Investigational, Once-Daily, Ribavirin-Free, Pan-Genotypic Regimen of ABT-493 and ABT-530 for Hepatitis C Genotypes 1-6

