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Collaboration Between AbbVie, Biogen and Pfizer Creates World’s Largest Browsable Resource Linking Rare Protein-Coding Genetic Variants to Human Health and Disease
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AbbVie to Host Second-Quarter 2021 Earnings Conference Call
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AbbVie (ABBV) Announces Upadacitinib Met Primary and All Secondary Endpoints in the 52-Week Phase 3 Maintenance Study in Ulcerative Colitis Patients
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Upadacitinib (RINVOQ®) Met the Primary and All Secondary Endpoints in the 52-Week Phase 3 Maintenance Study in Ulcerative Colitis Patients
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AbbVie Gastroenterology Pipeline to be Featured at the 16th Congress of European Crohn's and Colitis Organisation (ECCO)
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AbbVie (ABBV) Announces FDA Will Not Meet PDUFA Action Dates for RINVOQ sNDAs
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AbbVie Provides Update Regarding RINVOQ® (upadacitinib) in Psoriatic Arthritis and Ankylosing Spondylitis in the U.S.
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AbbVie (ABBV) Announces CHMP Recommends Approval of RINVOQ (upadacitinib) for the Treatment of Atopic Dermatitis
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CHMP Recommends Approval of RINVOQ® (upadacitinib) for the Treatment of Atopic Dermatitis
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Alpine Immune Sciences (ALPN) Doses First Patient in Synergy, ALPN-101 Phase 2 Lupus Clinical Trial, $45M Milestone Achieved
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AbbVie (ABBV) Exercises Option to Acquire TeneoOne
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AbbVie Exercises Right to Acquire TeneoOne and Lead Asset TNB-383B for the Potential Treatment of Relapsed or Refractory Multiple Myeloma
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AbbVie Declares Quarterly Dividend
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IMBRUVICA® (ibrutinib) Plus VENCLEXTA®/VENCLYXTO® (venetoclax) Combination Shows Superior Progression-Free Survival Compared to Chlorambucil Plus Obinutuzumab in First-line Chronic Lymphocytic Leuk
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New Data Shows AbbVie's VENCLYXTO®/VENCLEXTA® Fixed Duration Combination Demonstrates Sustained Progression-Free Survival in Chronic Lymphocytic Leukemia Patients after Three Years off Treatment
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Allergan Aesthetics and BOTOX® Cosmetic (onabotulinumtoxinA) Put Real Stories at the Forefront in New Campaign
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AbbVie (ABBV) CAPTIVATE Study Shows an IMBRUVICA Plus VENCLEXTA/VENCLYXTO Chemotherapy-Free Combination Has Potential to Provide Remission After Fixed-Duration Treatment for CLL
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CAPTIVATE Study Shows an IMBRUVICA® (ibrutinib) Plus VENCLEXTA®/VENCLYXTO® (venetoclax) Chemotherapy-Free Combination Has Potential to Provide Remission After Fixed-Duration Treatment for Chronic L
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AbbVie (ABBV) Results from IMBRUVICA® (ibrutinib) RESONATE-2 Study Provide Up to Seven Years of PF and OS Data in First-Line CLL
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Results from IMBRUVICA® (ibrutinib) RESONATE-2 Study Provide Up to Seven Years of Progression-Free and Overall Survival Data in First-Line Chronic Lymphocytic Leukemia (CLL)
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AbbVie to Present at the Goldman Sachs 42nd Annual Global Healthcare Conference
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AbbVie (ABBV) Phase 3 Maintenance Results of risankizumab 360 mg achieved the co-primary endpoints
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Phase 3 Maintenance Results Show Patients with Crohn's Disease Receiving Risankizumab (SKYRIZI®) Achieved Endoscopic Response and Clinical Remission at One Year
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AbbVie to Present Analysis Evaluating Continuous RINVOQ® (upadacitinib) Treatment in Psoriatic Arthritis for More Than One Year at EULAR 2021 Virtual Congress
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AbbVie (ABBV) Announces New Long-Term Efficacy and Safety Analyses Evaluating RINVOQ in Patients with Rheumatoid Arthritis to be Presented at EULAR 2021 Virtual Congress
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New Long-Term Efficacy and Safety Analyses Evaluating RINVOQ® (upadacitinib) in Patients with Rheumatoid Arthritis to be Presented at EULAR 2021 Virtual Congress
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AbbVie to Present at Bernstein's 37th Annual Strategic Decisions Conference
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AbbVie to Present Data from its Leading Migraine Portfolio at the 2021 American Headache Society (AHS) Annual Scientific Meeting
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AbbVie (ABBV) Receives EC Approval of VENCLYXTO in Combination with Hypomethylating Agent for Patients with Newly Diagnosed Acute Myeloid Leukemia Who Are Ineligible for Intensive Chemotherapy
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AbbVie Receives European Commission Approval of VENCLYXTO® (venetoclax) in Combination with a Hypomethylating Agent for Patients with Newly Diagnosed Acute Myeloid Leukemia Who Are Ineligible for Int
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AbbVie Showcases the Depth of its Rheumatology Portfolio with New Data Presented at the EULAR 2021 Virtual Congress of Rheumatology
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AbbVie (ABBV) Presents New Late-Breaking Data Analyses Showing Risankizumab Achieves Clinical Remission and Endoscopic Response at Week 12 in Patients with Moderate to Severe Crohn's Disease
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AbbVie Presents New Late-Breaking Data Analyses Showing Risankizumab (SKYRIZI®) Achieves Clinical Remission and Endoscopic Response at Week 12 in Patients with Moderate to Severe Crohn's Disease
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AbbVie (ABBV) Announces Lancet Publishes Results from Pivotal Global Phase 3 Program Evaluating RINVOQ in Atopic Dermatitis
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The Lancet Publishes Results from Pivotal Global Phase 3 Program Evaluating RINVOQ® (upadacitinib) in Atopic Dermatitis
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AbbVie to Present at the UBS Global Healthcare Virtual Conference
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AbbVie to Showcase Breadth of Oncology Portfolio and Pipeline at the 2021 ASCO and EHA Annual Congresses
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AbbVie to Present at the RBC Capital Markets Global Healthcare Conference
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AbbVie's (ABBV) Allergan Aesthetics to Acquire Soliton (SOLY)
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Allergan Aesthetics to Acquire Soliton, Expanding Body Contouring Portfolio
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Allergan Aesthetics to Acquire Soliton, Expanding Body Contouring Portfolio
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AbbVie Reports First-Quarter 2021 Financial Results
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Allergan, an AbbVie Company, to Share New Data Highlighting Latest Advancements in Eye Care at ARVO (Association for Research in Vision and Ophthalmology) 2021 Annual Virtual Meeting
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AbbVie (ABBV) Receives Positive CHMP Opinion for VENCLYXTO as Combination Regimen for Adult Patients with Newly Diagnosed Acute Myeloid Leukemia Who Are Ineligible for Intensive Chemotherapy
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AbbVie Receives Positive CHMP Opinion for VENCLYXTO® (venetoclax) as a Combination Regimen for Adult Patients with Newly Diagnosed Acute Myeloid Leukemia Who Are Ineligible for Intensive Chemotherapy
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AbbVie (ABBV) Submits Regulatory Applications for SKYRIZI (risankizumab) in Psoriatic Arthritis to FDA and EMA
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AbbVie Submits Regulatory Applications for SKYRIZI® (risankizumab) in Psoriatic Arthritis to FDA and EMA
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AbbVie to Present Data Across its Robust Neuroscience Portfolio at the 2021 American Academy of Neurology (AAN) Annual Meeting
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AbbVie (ABBV) Announces Extension of Review for sNDA of Upadacitinib for Treatment of Moderate to Severe Atopic Dermatitis
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AbbVie Announces Extension of Review for Supplemental New Drug Application of Upadacitinib for the Treatment of Moderate to Severe Atopic Dermatitis

