Compare · ABBV vs ZLAB
ABBV vs ZLAB
Side-by-side comparison of AbbVie Inc. (ABBV) and Zai Lab Limited (ZLAB): market cap, price performance, sector, and recent activity on the wire.
Summary
- Both ABBV and ZLAB operate in Biotechnology: Pharmaceutical Preparations (Health Care), so they compete in similar markets.
- ABBV is the larger of the two at $438.16B, about 198.8x ZLAB ($2.20B).
- Over the past year, ABBV is up 27.8% and ZLAB is down 43.7% - ABBV leads by 71.4 points.
- ABBV has been more active in the news (22 items in the past 4 weeks vs 16 for ZLAB).
- ABBV has more recent analyst coverage (25 ratings vs 11 for ZLAB).
- Company
- AbbVie Inc.
- Zai Lab Limited
- Price
- $244.71-1.33%
- $19.33-1.48%
- Market cap
- $438.16B
- $2.20B
- 1M return
- +8.96%
- +9.46%
- 1Y return
- +27.79%
- -43.66%
- Industry
- Biotechnology: Pharmaceutical Preparations
- Biotechnology: Pharmaceutical Preparations
- Exchange
- NYSE
- NASDAQ
- IPO
- 2012
- 2017
- News (4w)
- 22
- 16
- Recent ratings
- 25
- 11
AbbVie Inc.
AbbVie Inc. discovers, develops, manufactures, and sells pharmaceuticals in the worldwide. The company offers HUMIRA, a therapy administered as an injection for autoimmune and intestinal Behçet's diseases; SKYRIZI to treat moderate to severe plaque psoriasis in adults; RINVOQ, a JAK inhibitor for the treatment of moderate to severe active rheumatoid arthritis in adult patients; IMBRUVICA to treat adult patients with chronic lymphocytic leukemia (CLL), small lymphocytic lymphoma (SLL), mantle cell lymphoma, waldenström's macroglobulinemia, marginal zone lymphoma, and chronic graft versus host disease; VENCLEXTA, a BCL-2 inhibitor used to treat adults with CLL or SLL; and MAVYRET to treat patients with chronic HCV genotype 1-6 infection. It also provides CREON, a pancreatic enzyme therapy for exocrine pancreatic insufficiency; Synthroid used in the treatment of hypothyroidism; AndroGel for males diagnosed with symptomatic low testosterone; Linzess/Constella to treat irritable bowel syndrome with constipation and chronic idiopathic constipation; Lupron for the palliative treatment of advanced prostate cancer, endometriosis and central precocious puberty, and patients with anemia caused by uterine fibroids; and Botox therapeutic. In addition, the company offers ORILISSA, a nonpeptide small molecule gonadotropin-releasing hormone antagonist for women with moderate to severe endometriosis pain; Duopa and Duodopa, a levodopa-carbidopa intestinal gel to treat Parkinson's disease; Lumigan/Ganfort, a bimatoprost ophthalmic solution for the reduction of elevated intraocular pressure (IOP) in patients with open angle glaucoma (OAG) or ocular hypertension; Ubrelvy to treat migraine with or without aura in adults; Alphagan/ Combigan, an alpha-adrenergic receptor agonist for the reduction of IOP in patients with OAG; and Restasis, a calcineurin inhibitor immunosuppressant to increase tear production. The company was incorporated in 2012 and is based in North Chicago, Illinois.
Zai Lab Limited
Zai Lab Limited develops and commercializes therapies to treat oncology, autoimmune disorders, and infectious diseases primarily in Greater China. The company's commercial products include Zejula for the treatment of breast cancer and non-small cell lung cancer; Optune, a device that delivers tumor treating fields; and Qinlock to treat gastrointestinal stromal tumors. It also develops Odronextamab to treat follicular lymphoma, diffuse large B-cell lymphoma, and other lymphomas; Repotrectinib, a tyrosine kinase inhibitor (TKI) to target ROS1 and TRK A/B/C in TKI-naïve- or -pretreated cancer patients; Margetuximab for the treatment of breast and gastroesophageal cancers; and Bemarituzumab to treat gastric and gastroesophageal junction cancer. In addition, the company develops CLN-081 for the treatment of patients with EGFR exon 20 insertion NSCLC; TPX-0022, an orally bioavailable multi-targeted kinase inhibitor; Tebotelimab, a tetravalent IgG4 monoclonal antibody; Retifanlimab that inhibits interactions between PD-1 and its ligands; ZL-2309, an orally active, selective, and ATP-competitive cell division cycle 7 (CDC7) kinase inhibitor; ZL-1201, a humanized IgG4 monoclonal antibody; Efgartigimod to reduce disease-causing immunoglobulin G antibodies; ZL-1102, a human nanobody targeting interleukin-17; and Sulbactam/durlobactam for the treatment of serious infections caused by Acinetobacter. It has development, license, and collaboration agreements with GlaxoSmithKline; Paratek Bermuda, Ltd.; Five Prime Therapeutics, Inc.; Entasis Therapeutics Holdings, Inc.; Crescendo Biologics Ltd.; Novocure Limited; MacroGenics Inc.; Deciphera Pharmaceuticals, LLC; Incyte Corporation; Regeneron Ireland Designated Activity Company; Turning Point Therapeutics Inc; Cullinan Pearl Corp.; Takeda Pharmaceutical Company Limited; Schrödinger, Inc.; and argenx BV. The company was incorporated in 2013 and is headquartered in Shanghai, China.
Latest ABBV
- SkinMedica® Deepens Commitment to Regenerative Science with Continued Investment in Research and Development
- One Formula, One Platform: Inside the Preclinical Milestone Behind Conexeu's Move Into Medical Aesthetics
- AbbVie Inc. filed SEC Form 8-K: Results of Operations and Financial Condition, Financial Statements and Exhibits
- AbbVie Announces TEPKINLY® (epcoritamab) in Combination with Lenalidomide and Rituximab is Approved by the European Commission for the Treatment of Relapsed or Refractory Follicular Lymphoma
- SEC Form 4 filed by Director Rapp Edward J
- SEC Form 4 filed by Director Quaggin Susan E
- A Nasdaq-Listed Regenerative Tissue Company Just Opened a Lab: The Next Step in Scaling a Platform Built for a NEW Aesthetics Opportunity
- AbbVie Announces Positive Phase 3 Results for Epcoritamab Plus Lenalidomide in Patients with Relapsed or Refractory Diffuse Large B-Cell Lymphoma
- FDA Approval for SKYRIZI issued to ABBVIE INC
- FDA Approval for SKYRIZI issued to ABBVIE INC
Latest ZLAB
- Director Gaynor Richard bought $33,071 worth of American Depositary Shares (1,736 units at $19.05), increasing direct ownership by 2% to 80,737 units (SEC Form 4)
- Chairperson & CEO Du Ying converted options into 29,048 units of American Depositary Shares and covered exercise/tax liability with 11,431 units of American Depositary Shares, increasing direct ownership by 1% to 1,221,401 units (SEC Form 4)
- Chairperson & CEO Du Ying sold $130,220 worth of American Depositary Shares (7,026 units at $18.53) and converted options into 17,970 units of American Depositary Shares, increasing direct ownership by 0.92% to 1,203,784 units (SEC Form 4)
- Chief Legal Officer Edmondson Frazor Titus Iii converted options into 14,600 units of American Depositary Shares and sold $71,642 worth of American Depositary Shares (4,103 units at $17.46), increasing direct ownership by 53% to 30,346 units (SEC Form 4)
- Chairperson & CEO Du Ying converted options into 58,800 units of American Depositary Shares and sold $428,545 worth of American Depositary Shares (24,543 units at $17.46), increasing direct ownership by 3% to 1,192,840 units (SEC Form 4)
- Chief Financial Officer Chen Yajing converted options into 6,250 units of American Depositary Shares and sold $39,532 worth of American Depositary Shares (2,264 units at $17.46), increasing direct ownership by 13% to 35,691 units (SEC Form 4)
- Director Lis William sold $127,354 worth of American Depositary Shares (7,040 units at $18.09) as part of a pre-agreed trading plan, decreasing direct ownership by 12% to 50,437 units (SEC Form 4)
- Director Wirth Peter was granted 22,371 units of American Depositary Shares, increasing direct ownership by 6% to 416,121 units (SEC Form 4)
- Director Diekman John D was granted 22,371 units of American Depositary Shares, increasing direct ownership by 22% to 122,140 units (SEC Form 4)
- Director Morrison Scott W was granted 22,371 units of American Depositary Shares, increasing direct ownership by 65% to 56,904 units (SEC Form 4)