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AbbVie and Allergan Receive Second Request from Federal Trade Commission on Pending Transaction
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AbbVie Receives FDA Approval of MAVYRET® (glecaprevir/pibrentasvir) to Shorten Treatment Duration to Eight Weeks for Treatment-Naïve Patients with Chronic Hepatitis C and Compensated Cirrhosis Acros
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AbbVie to Present New and Updated Data From 22 Abstracts, Including Two Late-Breaking Abstracts for ABBV-951 and DUODOPA® (levodopa/carbidopa intestinal gel), at the International Congress of Parkins
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AbbVie Declares Quarterly Dividend
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AbbVie (ABBV) Discontinues Rova-T After No Surviable Benefit Versus Placebo in SCLC
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AbbVie Discontinues Rovalpituzumab Tesirine (Rova-T) Research and Development Program
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AbbVie to Present at the Morgan Stanley Healthcare Conference
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AbbVie Receives FDA Approval of RINVOQ™ (upadacitinib), an Oral JAK Inhibitor For The Treatment of Moderate to Severe Rheumatoid Arthritis
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AbbVie (ABBV) Submits NDA to US FDA for Investigational Elagolix for Management of Heavy Menstrual Bleeding Associated with Uterine Fibroids in Women
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AbbVie Submits New Drug Application to US FDA for Investigational Elagolix for Management of Heavy Menstrual Bleeding Associated with Uterine Fibroids in Women
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AbbVie Reports Second-Quarter 2019 Financial Results
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Bristol-Myers Squibb (BMY) Receives Positive CHMP Opinion Recommending Approval of Empliciti Plus Pomalidomide and Low-Dose Dexamethasone for Treatment of Patients with R/R MM
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AbbVie (ABBV) Announces Acquisition of Mavupharma
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AbbVie Enhances Early Stage Oncology Pipeline with Acquisition of Mavupharma
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AbbVie to Host Second-Quarter 2019 Earnings Conference Call
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AbbVie (ABBV) Announces Agreement to Acquire Allergan (AGN) in $63 Billion Deal
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AbbVie to Acquire Allergan in Transformative Move for Both Companies
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AbbVie (ABBV) Reports FDA to Lift Partial Clinical Hold on CANOVA (M13-494), a Phase 3 Study of Venetoclax
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AbbVie Announces US FDA Lifts Partial Clinical Hold on Phase 3 Study of Venetoclax in Patients with Multiple Myeloma Positive for the t(11;14) Genetic Abnormality
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AbbVie Declares Quarterly Dividend
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AbbVie (ABBV) Highlights New Long-Term Data from Upadacitinib Phase 3 Studies in Rheumatoid Arthritis Including Results on Clinical Remission at 48 Weeks
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New Long-Term Data from Upadacitinib Phase 3 Studies in Rheumatoid Arthritis Including Results on Clinical Remission at 48 Weeks Presented at EULAR
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AbbVie (ABBV) Says New Two-Year Data at the 24th World Congress of Dermatology Shows SKYRIZI Maintains Complete Skin Clearance
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New Two-Year Data at the 24th World Congress of Dermatology Shows SKYRIZI™ (risankizumab) Maintains Complete Skin Clearance
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AbbVie to Present at the Goldman Sachs Global Healthcare Conference
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AbbVie (ABBV) Presents Data from Venetoclax Chemotherapy-Free Combination Regimen for Patients with Previously Untreated CLL
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AbbVie Presents Data from Venetoclax Chemotherapy-Free Combination Regimen for Patients with Previously Untreated Chronic Lymphocytic Leukemia
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AbbVie (ABBV) Presents Results from Several Studies and Clinical Trials Investigating Medicines Across More than 15 Cancers at the 2019 ASCO and EHA
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AbbVie Presents Results from Several Studies and Clinical Trials Investigating Medicines Across More than 15 Cancers at the 2019 ASCO and EHA Meetings
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AbbVie (ABBV) Provides Update on Depatuxizumab Mafodotin, IDMC Recommended Study be Stopped due to Lack of Survival Benefit
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AbbVie Provides Update on Depatuxizumab Mafodotin (Depatux-M), an Investigational Medicine for Newly Diagnosed Glioblastoma, an Aggressive Form of Brain Cancer
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AbbVie (ABBV) Announces FDA Approval of VENCLEXTA as Chemotherapy-Free Combination Regimen for Previously Untreated CLL Patients
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AbbVie Announces US FDA Approval of VENCLEXTA® (venetoclax) as a Chemotherapy-Free Combination Regimen for Previously Untreated Chronic Lymphocytic Leukemia Patients
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AbbVie (ABBV) Resolves HUMIRA U.S. Patent Litigation with BI
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AbbVie Resolves HUMIRA® (adalimumab) U.S. Patent Litigation with Boehringer Ingelheim
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AbbVie to Present at the UBS Global Healthcare Conference
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AbbVie (ABBV) Announces EC Approves SKYRIZI for Treatment of Moderate to Severe Plaque Psoriasis
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European Commission Approves SKYRIZI™ (risankizumab) for the Treatment of Moderate to Severe Plaque Psoriasis
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AbbVie to Present New and Updated Data of Investigational Medicines for Parkinson's Disease and Multiple Sclerosis at 2019 American Academy of Neurology Annual Meeting
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AbbVie Reports First-Quarter 2019 Financial Results
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AbbVie Expands Immunology Portfolio in the U.S. with FDA Approval of SKYRIZI™ (risankizumab-rzaa) for Moderate to Severe Plaque Psoriasis
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AbbVie to Host First-Quarter 2019 Earnings Conference Call
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AbbVie Announces First Regulatory Approval of SKYRIZI™ (risankizumab) for the Treatment of Plaque Psoriasis, Generalized Pustular Psoriasis and Erythrodermic Psoriasis and Psoriatic Arthritis in Jap
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AbbVie (ABBV) Announces Partial Clinical Hold on VENCLEXTA/VENCLYXTO Trials
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AbbVie Provides Update on VENCLEXTA®/VENCLYXTO® (venetoclax) Multiple Myeloma Program
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AbbVie (ABBV) Announces Milestones for Phase 3 CLL14 Venetoclax Study of Fixed Duration Treatment in Previously-Untreated CLL Patients
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AbbVie Announces Multiple Milestones for Phase 3 CLL14 Venetoclax Study of Fixed Duration Treatment in Previously-Untreated Chronic Lymphocytic Leukemia Patients
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AbbVie to Present at the Barclays Global Healthcare Conference
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AbbVie (ABBV) Receives CHMP Positive Opinion for Risankizumab for Treatment of Moderate to Severe Plaque Psoriasis
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AbbVie Receives CHMP Positive Opinion for Risankizumab (SKYRIZI™) for the Treatment of Moderate to Severe Plaque Psoriasis

