North Chicago, IL, United States · Est. 2012 · 50,000 employees
Research-driven biopharmaceutical company focused on advanced therapies for complex diseases.
Pipeline Programs↗
Distinct drugs in development (Preclinical–Phase 3)
Indications↗
Distinct diseases across all programs
Clinical Trials↗
All sponsored trials (all statuses)
Orange Book Patents
Across 19 drugs with upcoming expirations
Pipeline
By Phase
73 drugs in development
By Therapeutic Area
top 6
R&D Momentum
94/100
Pipeline Velocity
76/100
Trial Completion Rate
86/100
Pipeline Concentration
16/100
Pipeline Freshness
70/100
Strategic Signals
Activity
Last 14 days
A Phase 3 Randomized, Placebo-controlled, Double-blind Program to Evaluate Efficacy and Safety of Upadacitinib in Adult and Adolescent Subjects With Severe Alopecia Areata
An Open-Label, Randomized, Controlled, Global Phase 3 Study Comparing Telisotuzumab Adizutecan (ABBV-400) Plus Bevacizumab to LONSURF (Trifluridine and Tipiracil) Plus Bevacizumab in Subjects With Refractory Metastatic Colorectal Cancer
A Multicenter, Phase 1b, Open-label Study to Evaluate Dose Optimization Measures and Safety of Etentamig (ABBV-383) in Subjects With Relapsed or Refractory Multiple Myeloma
A Phase 2, Open-Label, Randomized, Master Protocol Dose Optimization Study to Evaluate Safety and Efficacy of Multiple Treatment Combinations With Mirvetuximab Soravtansine in Subjects With Ovarian Cancer
A Phase 2, Open-Label, Randomized, Master Protocol Study to Evaluate Safety and Efficacy of Multiple Treatment Combinations With Telisotuzumab Adizutecan in Subjects With Metastatic Colorectal Cancer
A Phase 1, Open-label, Single Dose, Crossover Study to Assess the Relative Bioavailability of Emraclidine Formulations in Healthy Adult Subjects
An Open-label Multi-Cohort Phase 1b/2 Study to Evaluate the Safety, Efficacy, and Optimal Dose of Telisotuzumab Adizutecan in Combination With a PD-1 Immune Checkpoint Inhibitor in Advanced or Metastatic Non-Squamous NSCLC With No Prior Treatment for Advanced Disease and No Actionable Genomic Alterations
First-in-Human Study to Evaluate the Safety, Pharmacokinetics, and Preliminary Efficacy of the BTK Degrader, ABBV-101, in Participants With B-cell Malignancies
Observational Study of the Use of Venetoclax in Patients With Chronic Lymphocytic Leukemia (CLL) Under Real-Life Setting in Austria, Germany and Switzerland
Safety, Tolerability, Pharmacokinetics, and Exploratory Efficacy of ABBV-6628 in Subjects With Geographic Atrophy Secondary to Age-Related Macular Degeneration
A Phase 1b Study of the Safety and Pharmacokinetics of Pivekimab Sunirine in Pediatric Subjects With Relapsed or Refractory Acute Myeloid Leukemia (AML)
Details
Company Overview
$310.0B
Mkt Cap
$54.3B
Revenue
$5.5B
Cash
Therapeutic Focus
Recent SEC Filings
AbbVie Inc. (ABBV) (CIK 0001551152)
Pipeline
Regulatory
Lupron — LEUPROLIDE ACETATE FOR DEPOT SUSPENSION
Application NDA205054 (NDA)
Orilissa — ORILISSA
Application NDA210450 (NDA)
Ubrelvy — UBRELVY
Application NDA211765 (NDA)
Saphris — SECUADO
Application NDA212268 (NDA)
Rinvoq — RINVOQ
Application NDA211675 (NDA)
Skyrizi — Skyrizi
Application 761105 (BLA)
SKYRIZI — SKYRIZI
Application BLA761105 (BLA)
Lupron — FENSOLVI KIT
Application NDA213150 (NDA)
Zolymbus — DURYSTA
Application NDA211911 (NDA)
Qulipta — QULIPTA
Application NDA215206 (NDA)
Lupron — CAMCEVI KIT
Application NDA211488 (NDA)
SKYRIZI — SKYRIZI
Application BLA761262 (BLA)
Celexa — CITALOPRAM HYDROBROMIDE
Application NDA215428 (NDA)
Rinvoq — RINVOQ LQ
Application NDA218347 (NDA)
Vraylar — VRAYLAR
Application NDA204370 (NDA)
Zolymbus — ZOLYMBUS
Application NDA217307 (NDA)
Lexapro — ESCITALOPRAM
Application NDA219130 (NDA)
Lupron — CAMCEVI ETM
Application NDA219745 (NDA)
EMRELIS — EMRELIS
Application BLA761384 (BLA)
HydroDIURIL — INZIRQO
Application NDA219141 (NDA)
AbbVie Inc. (ABBV) (CIK 0001551152)
Accession: 001-35565
Data sources: ClinicalTrials.gov (NIH) · OpenFDA (FDA) · ChEMBL (EMBL-EBI) · Open Targets (EBI/Sanger) · MedlinePlus (NIH) · PubMed (NIH) · SEC EDGAR (SEC)