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 Showcases Commitment to Research and Innovation in Dermatology at the 25th European Academy of Dermatology and Venereology Congress
-
AbbVie Announces Submission of a Supplemental New Drug Application for Ibrutinib (IMBRUVICA®) for Treatment of Marginal Zone Lymphoma
-
AbbVie (ABBV) Presents VIEKIRAX + EXVIERA Phase 3 Data in HCV; Sustained Virologic Response Rates Noted
-
AbbVie Presents Data on Eight-Week Treatment of VIEKIRAX® (ombitasvir/paritaprevir/ritonavir tablets) + EXVIERA® (dasabuvir tablets) in Patients with Genotype 1b Chronic Hepatitis C
-
Karolinska Development portfolio company BioArctic enters into Collaboration with AbbVie for Parkinson's Disease Research
-
BioArctic AB: BioArctic Enters into Collaboration with AbbVie for Parkinson’s Disease Research
-
Biogen (BIIB), AbbVie (ABBV) Announce Significant ZINBRYTA Data in NEDA vs AVONEX
-
New Data Presented at ECTRIMS Reinforce Efficacy of ZINBRYTA™ (Daclizumab) and Support Long-Term Safety Profile
-
AbbVie Declares Quarterly Dividend
-
AbbVie Declares Quarterly Dividend
-
AbbVie to Present at the Morgan Stanley Global Healthcare Conference
-
AbbVie to Present at the Morgan Stanley Global Healthcare Conference
-
AbbVie Reports Second-Quarter 2016 Financial Results
-
AbbVie (ABBV) Initiates Phase 3 Study of Venetoclax in Patients with Relapsed or Refractory
-
AbbVie Announces Initiation of Phase 3 Study of Venetoclax in Patients with Relapsed or Refractory Multiple Myeloma
-
AbbVie's (ABBV) VIEKIRA XR NDA Approved by U.S. FDA
-
AbbVie Receives U.S. FDA Approval of Once-Daily VIEKIRA XR™ (dasabuvir, ombitasvir, paritaprevir and ritonavir) for the Treatment of Genotype 1 Chronic Hepatitis C
-
AbbVie (ABBV), Bristol-Myers Squibb (BMY) to Collaborate on Rova-T + Opdivo Combo
-
AbbVie and Bristol-Myers Squibb Announce Oncology Clinical Collaboration to Evaluate the Combination of Rova-T plus Opdivo and Opdivo + Yervoy Regimen
-
AbbVie and Bristol-Myers Squibb Announce Oncology Clinical Collaboration to Evaluate the Combination of Rova-T plus Opdivo and Opdivo + Yervoy Regimen
-
AbbVie (ABBV) Receives Positive CHMP Opinion on VIEKIRAX in GT4 HCV (ENTA)
-
CHMP Grants Positive Opinion for Shorter Treatment Duration with AbbVie's VIEKIRAX® (ombitasvir/paritaprevir/ritonavir tablets) for Patients with Genotype 4 Chronic Hepatitis C with Compensated Cirrh
-
AbbVie's (ABBV) ABT-414 Granted FDA Rare Pediatric Disease Designation as DIPG Treatment
-
AbbVie Receives U.S. FDA Rare Pediatric Disease Designation for Investigational ABT-414 for the Treatment of a Type of Pediatric Brain Tumor known as Diffuse Intrinsic Pontine Glioma (DIPG)
-
AbbVie (ABBV) to Present Positive HUMIRA Phase 3 Data in Moderate to Severe Fingernail Psoriasis
-
AbbVie Presents Initial Data from Pivotal Phase-3 Trial Evaluating the Efficacy and Safety of HUMIRA® (adalimumab) for Moderate to Severe Fingernail Psoriasis in Adult Patients at Psoriasis 2016 Cong
-
Biogen (BIIB), AbbVie (ABBV) Receive Marketing Approval in Europe for ZINBRYTA as MS Treatment
-
Biogen and AbbVie’s Once-Monthly ZINBRYTA™ (Daclizumab) Approved in European Union for Treatment of Multiple Sclerosis
-
AbbVie to Host Second-Quarter Earnings Conference Call
-
AbbVie's (ABBV) HUMIRA Receives FDA Approval as Non-Infectious Intermediate, Posterior and Panuveitis Treatment
-
AbbVie's HUMIRA® (adalimumab) Receives U.S. Food and Drug Administration Approval to Treat Adults with Non-Infectious Intermediate, Posterior and Panuveitis
-
AbbVie's (ABBV) Ibrutinib Receives Fourth FDA Breakthrough Therapy Designation
-
AbbVie Announces Fourth Breakthrough Therapy Designation Granted by the U.S. Food and Drug Administration (FDA) for Ibrutinib (IMBRUVICA®) for Chronic Graft-Versus-Host-Disease (cGVHD), a Rare Condit
-
AbbVie Teams Up with Leading Nonprofit Organizations to Give Back to Underserved Local Communities
-
AbbVie Declares Quarterly Dividend
-
AbbVie Scholarship Programs Recognize Exceptional Students Living with Chronic Inflammatory Diseases
-
New AbbVie Global Campaign Aims to Provide Educational Resources for Millions Living with Painful, Chronic Skin Disease
-
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

