ABBVIE
- Country
- 🇺🇸United States
- Ownership
- -
- Established
- 2013-01-01
- Employees
- -
- Market Cap
- $346B
- Website
- http://www.abbvie.com
Clinical Trials
1.1k
Trial Phases
5 Phases
Drug Approvals
0
Drug Approvals
No drug approvals found
This company may not have drug approvals in our database
Clinical Trials
Distribution across different clinical trial phases (812 trials with phase data)• Click on a phase to view related trials
A Study to Assess Adverse Events and Change in Disease Activity of Multiple Treatment Combinations With Intravenous Mirvetuximab Soravtansine in Adult Participants With Ovarian Cancer
- Conditions
- Ovarian Cancer
- Interventions
- First Posted Date
- 2025-07-11
- Last Posted Date
- 2025-07-11
- Lead Sponsor
- AbbVie
- Target Recruit Count
- 320
- Registration Number
- NCT07059845
Cross-sectional Study to Characterize Real World Burden of Disease in Patients With Vitiligo in China
- Conditions
- Non-Segmental Vitiligo
- First Posted Date
- 2025-07-10
- Last Posted Date
- 2025-07-10
- Lead Sponsor
- AbbVie
- Target Recruit Count
- 100
- Registration Number
- NCT07058051
Study to Assess Adverse Events and Change in Disease Activity of Oral Venetoclax in Combination With Subcutaneous (SC) or Intravenous (IV) Azacitidine in Newly Diagnosed Adult Participants With Acute Myeloid Leukemia (AML) Who Are Ineligible for Standard Induction Therapy in India
- Conditions
- Acute Myeloid Leukemia
- Interventions
- First Posted Date
- 2025-07-01
- Last Posted Date
- 2025-07-01
- Lead Sponsor
- AbbVie
- Target Recruit Count
- 100
- Registration Number
- NCT07044687
Study to Assess Change in Quality of Life of Risankizumab Treatment in Adult Participants With Moderate-to-Severe Plaque Psoriasis
- Conditions
- Plaque Psoriasis
- First Posted Date
- 2025-06-26
- Last Posted Date
- 2025-06-26
- Lead Sponsor
- AbbVie
- Target Recruit Count
- 700
- Registration Number
- NCT07039110
A Study to Assess Safety and Effectiveness of HArmonyCa Lidocaine Injectable Gel for Restoration and/or Creation of Mid-Face Volume in Adult Participants
- Conditions
- Mid Face Volume Deficit
- First Posted Date
- 2025-06-24
- Last Posted Date
- 2025-06-24
- Lead Sponsor
- AbbVie
- Target Recruit Count
- 252
- Registration Number
- NCT07032597
- Locations
- 🇨🇳
Beijing Hospital /ID# 272476, Beijing, Beijing, China
🇨🇳Peking Union Medical College Hospital (West) - Xidan Campus /ID# 272480, Beijing, Beijing, China
🇨🇳Union Hospital Tongji Medical College Huazhong University of Science and Technol /ID# 272631, Wuhan, Hubei, China
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News
Everest Medicines Advances AI-Powered mRNA Platform with Cancer Vaccine Breakthroughs
Everest Medicines unveiled major breakthroughs in its proprietary AI-powered mRNA platform during its 2025 R&D Day, showcasing a fully integrated system spanning antigen design to manufacturing.
Oxford BioTherapeutics and Boehringer Ingelheim Advance Third Oncology Drug Candidate to IND-Enabling Studies
Oxford BioTherapeutics announced that Boehringer Ingelheim has selected a third drug candidate targeting OB33 to advance into IND-enabling studies under their ongoing collaboration.
Neurocrine Biosciences Initiates Phase 1 Trial for Long-Acting CAH Treatment NBIP-01435
Neurocrine Biosciences has launched a Phase 1 first-in-human clinical study evaluating NBIP-01435, a long-acting corticotropin-releasing factor type 1 receptor antagonist for congenital adrenal hyperplasia treatment.
AbbVie Acquires Capstan Therapeutics for $2.1 Billion to Advance In Vivo CAR-T Technology for Autoimmune Diseases
AbbVie has agreed to acquire Capstan Therapeutics for up to $2.1 billion to gain access to CPTX2309, a potential first-in-class treatment for autoimmune diseases currently in Phase 1 trials.
AbbVie Acquires In Vivo CAR-T Developer Capstan Therapeutics for Up to $2.1 Billion
AbbVie has agreed to acquire cell therapy developer Capstan Therapeutics in a deal worth up to $2.1 billion in cash, gaining access to innovative in vivo CAR-T technology.
FDA Accepts Review of SKINVIVE by Juvéderm for Neck Line Treatment Expansion
Allergan Aesthetics has received FDA acceptance for review of its supplemental premarket approval application to expand SKINVIVE by Juvéderm's indication from cheek smoothness to include neck line treatment.
Alzheimer's Drug Market Sees 780% Investment Surge Following Leqembi and Kisunla Approvals
Total M&A deal value in Alzheimer's disease jumped from $2 billion in 2022 to $18 billion in 2024, representing a 780% increase following the approval of disease-modifying treatments.
Prokaryotics Secures Global Rights to Novel Gram-Negative Antibiotic Potentiator NAB741
Prokaryotics Inc. has entered into a licensing agreement with Northern Antibiotics for worldwide rights to develop NAB741, a non-bioactive polymyxin designed to enhance antibiotic efficacy against Gram-negative bacteria.
CNS Oligonucleotide Licensing Deals Surge 339% to $2.81 Billion in 2024
Licensing agreements for CNS-targeted oligonucleotide therapeutics increased 339% from 2023 to 2024, reaching $2.81 billion in total deal value according to GlobalData's analysis.
Simcere Zaiming Initiates US Phase 1 Trial of Trispecific Antibody SIM0500 for Relapsed/Refractory Multiple Myeloma
Simcere Zaiming has dosed the first US patient in a Phase 1 trial of SIM0500, a trispecific antibody targeting GPRC5D, BCMA, and CD3 for relapsed/refractory multiple myeloma treatment.