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AbbVie (ABBV) Issues Positive Update on ABT-493 and ABT-530 w/ RBV in HCV GT1 (ENTA)
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AbbVie's Investigational, Pan-Genotypic Regimen of ABT-493 and ABT-530 Shows High SVR Rates in Genotype 1 Hepatitis C Patients Who Failed Previous Therapy with Direct-Acting Antivirals
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AbbVie Announces Real-World Data with VIEKIRAX® (ombitasvir/paritaprevir/ritonavir tablets) and EXVIERA® (dasabuvir tablets) from Large German Hepatitis C-Registry
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AbbVie Announces High SVR Rates with VIEKIRAX® (ombitasvir/paritaprevir/ritonavir tablets) + EXVIERA® (dasabuvir tablets) Regardless of the Presence of Resistance-Associated Variants Prior to Treatm
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AbbVie Receives FDA Accelerated Approval of Venclexta™ (venetoclax) Tablets, the First BCL-2 Inhibitor in Relapsed/Refractory Chronic Lymphocytic Leukemia Patients with 17p Deletion
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AbbVie (ABBV) Announces Receipt of Accelerated FDA Approval for Venclexta in CLL
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AbbVie Receives FDA Accelerated Approval of Venclexta™ (venetoclax) Tablets, the First BCL-2 Inhibitor in Relapsed/Refractory Chronic Lymphocytic Leukemia Patients with 17p Deletion
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AbbVie to Host First-Quarter Earnings Conference Call
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AbbVie (ABBV) Affirms Receipt of Positive EMA CHMP Opinion for HUMIRA in Crohn's Disease
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AbbVie Receives CHMP Positive Opinion for HUMIRA® (adalimumab) for the Treatment of Pediatric Patients, from Six Years of Age, with Moderately to Severely Active Crohn's Disease
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AbbVie to Present Data on VIEKIRAX® (ombitasvir/paritaprevir/ritonavir tablets) and EXVIERA® (dasabuvir tablets) and Investigational, Pan-Genotypic Regimen at The International Liver Congress™ 201
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AbbVie to Present at Barclays Global Healthcare Conference
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AbbVie (ABBV), Boehringer Ingelheim Enter Agreement for BI 655066 Development, Commercialization
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AbbVie and Boehringer Ingelheim announce global collaboration on promising immunology compounds
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AbbVie and Boehringer Ingelheim announce global collaboration on promising immunology compounds
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AbbVie (ABBV), J&J (JNJ) Announce FDA Approval of IMBRUVICA as First-Line CLL Treatment
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IMBRUVICA® (ibrutinib) Approved by U.S. FDA for the First-line Treatment of Chronic Lymphocytic Leukemia
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AbbVie Announces New Dermatology Research from More Than 35 Presentations on HUMIRA® (Adalimumab), Long-Term and Real-World Data at the American Academy of Dermatology 2016 Annual Meeting
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AbbVie to Present at Cowen and Company 36th Annual Health Care Conference
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AbbVie (ABBV) Announces Positive CHMP Opinion for VIEKIRAX Without Ribavirin in HCV
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AbbVie Receives CHMP Positive Opinion for VIEKIRAX® (ombitasvir/paritaprevir/ritonavir tablets) + EXVIERA® (dasabuvir tablets) Without Ribavirin for the Treatment of Chronic Hepatitis C in Genotype
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AbbVie (ABBV) Announces Receipt of EMA Orphan Drug Designation for Venetoclax as AML Treatment
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AbbVie Receives EMA Orphan Drug Designation for Investigational Compound Venetoclax for the Treatment of Acute Myeloid Leukemia (AML)
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Notable Analyst Rating Changes 2/23: (ABBV) (TWTR) (NLY) Upgraded; (EVEP) (FCX) (X) Downgraded
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AbbVie Declares Quarterly Dividend
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AbbVie (ABBV) Announces Second Elagolix Phase 3 Met co-Primary Endpoints in Endometriosis (NBIX)
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AbbVie Announces Positive Top-Line Results From Second Phase 3 Study Investigating Elagolix in Patients with Endometriosis
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Bristol-Myers Squibb (BMY), AbbVie (ABBV) Announce Receipt of Positive CHMP Opinion for Empliciti as Multiple Myeloma Treatment
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Bristol-Myers Squibb and AbbVie Receive Positive CHMP Opinion for Investigational Antibody, Empliciti (elotuzumab), for the Treatment of Multiple Myeloma in Patients Who Have Received at Least One Pri
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AbbVie Reports Full-Year 2015 and Fourth-Quarter Financial Results
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AbbVie (ABBV) Announces Receipt of FDA Breakthrough Therapy Designation for Venetoclax Combo in Certain AML
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AbbVie (ABBV), Neurocrine Bio (NBIX) Initiate Enrollment in Phase 3 Study of Elagolix in Patients with Uterine Fibroids
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AbbVie Initiates Enrollment in Phase 3 Clinical Program for Elagolix in Patients with Uterine Fibroids
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Venetoclax Receives 3rd Breakthrough Therapy Designation from the FDA for the Combination Treatment of Patients with Untreated Acute Myeloid Leukemia not Eligible for Standard Induction Chemotherapy
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AbbVie (ABBV) and MD Anderson Partner on Cancer Immunotherapy
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MD Anderson, AbbVie Connect to Advance Cancer Immunotherapy
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AbbVie's (ABBV) Venetoclax Combo Granted FDA Breakthrough Therapy Designation for r/r CLL
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AbbVie's Venetoclax Receives Breakthrough Therapy Designation from FDA in Combination with Rituximab for the Treatment of Patients with Relapsed/Refractory Chronic Lymphocytic Leukemia
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AbbVie (ABBV) Announces Regulatory Acceptance of Venetoclax Apps in Europe, U.S.
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U.S. and European Regulators Accept Applications for AbbVie's Venetoclax, the First Potential BCL-2 Inhibitor for Chronic Lymphocytic Leukemia
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AbbVie Initiates Enrollment of Six Global Phase 3 Clinical Studies for Once-Daily, Pan-Genotypic Hepatitis C Regimen
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AbbVie (ABBV) Commences ABT-494 Phase 3 as RA Treatment
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AbbVie Announces the Launch of Robust Phase 3 Clinical Trial Program Evaluating ABT-494, an Investigational Selective JAK1 Inhibitor, for the Treatment of Rheumatoid Arthritis
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AbbVie to Host Fourth-Quarter and Full-Year 2015 Earnings Conference Call
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AbbVie (ABBV) Says FDA Gives Priority Review for Supplemental New Drug Application for VIEKIRA PAK
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U.S. FDA Grants Priority Review to AbbVie for Supplemental New Drug Application for VIEKIRA PAK® (ombitasvir, paritaprevir, ritonavir tablets; dasabuvir tablets) without Ribavirin in Genotype 1b Chro
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AbbVie to Present at the 34th Annual J.P. Morgan Healthcare Conference
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Data from IMBRUVICA Phase 2 RESONATE-17 Presented at ASH 2015; High ORR Noted (JNJ) (ABBV)
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AbbVie (ABBV) Announces Significant PFS Data from IMBRUVICA Phase 3 RAY
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IMBRUVICA® (Ibrutinib) Phase 3 RAY Data Show Significant Reductions in Disease Progression versus Temsirolimus in Relapsed/Refractory Mantle Cell Lymphoma Patients

