Compare · MGNX vs XNCR
MGNX vs XNCR
Side-by-side comparison of MacroGenics Inc. (MGNX) and Xencor Inc. (XNCR): market cap, price performance, sector, and recent activity on the wire.
Summary
- Both MGNX and XNCR operate in Biotechnology: Pharmaceutical Preparations (Health Care), so they compete in similar markets.
- XNCR is the larger of the two at $2.18B, about 8.2x MGNX ($265.6M).
- Over the past year, MGNX is up 131.0% and XNCR is up 270.2% - XNCR leads by 139.2 points.
- MGNX has been more active in the news (7 items in the past 4 weeks vs 3 for XNCR).
- MGNX has more recent analyst coverage (25 ratings vs 22 for XNCR).
- Company
- MacroGenics Inc.
- Xencor Inc.
- Price
- $4.17+3.73%
- $29.30+0.98%
- Market cap
- $265.6M
- $2.18B
- 1M return
- +5.04%
- +47.61%
- 1Y return
- +131.02%
- +270.18%
- Industry
- Biotechnology: Pharmaceutical Preparations
- Biotechnology: Pharmaceutical Preparations
- Exchange
- NASDAQ
- NASDAQ
- IPO
- 2013
- 2013
- News (4w)
- 7
- 3
- Recent ratings
- 25
- 22
MacroGenics Inc.
MacroGenics, Inc., a biopharmaceutical company, discovers and develops antibody-based therapeutics to treat cancer in the United States. The company's approved product is MARGENZA (margetuximab-cmkb), a human epidermal growth factor receptor 2 (HER2) receptor antagonist indicated, in combination with chemotherapy, for the treatment of adult patients with metastatic HER2-positive breast cancer who have received two or more prior anti-HER2 regimens. Its pipeline of immuno-oncology product candidates includes Margetuximab, a monoclonal antibody, which is in Phase II/III clinical trial for the treatment of breast and gastroesophageal cancers. The company is also developing Flotetuzumab, a DART molecule that recognizes CD123 and CD3 for treating acute myeloid leukemia; Retifanlimab, an investigational monoclonal antibody targeting metastatic squamous cell carcinoma of the anal canal and metastatic non-small cell lung cancer; Enoblituzumab, a monoclonal antibody that targets B7-H3; and Tebotelimab, an investigational tetravalent DART molecule for PD-1 and lymphocyte-activation gene 3. In addition, it is developing MGC018, an antibody drug conjugate (ADC), which targets solid tumors expressing B7-H3; MGD019, a monoclonal antibody that targets the immune checkpoints PD-1 and cytotoxic T-lymphocyte-associated protein 4; and IMGC936, an ADC that targets ADAM9, a cell surface protein over-expressed in various solid tumor types. Further, the company's non-immuno-oncology clinical product candidates include MGD014, a DART molecule to target the envelope protein of human immunodeficiency virus infected cells and T cells; Teplizumab for the treatment of type 1 diabetes; and PRV-3279, a CD32B Ã CD79B DART molecule for the treatment of autoimmune indications. It has collaborations with Incyte Corporation; Zai Lab Limited; I-Mab Biopharma; Janssen Biotech, Inc.; and Alligator Bioscience AB (publ). The company was incorporated in 2000 and is headquartered in Rockville, Maryland.
Xencor Inc.
Xencor, Inc., a clinical stage biopharmaceutical company, focuses on the discovery and development of engineered monoclonal antibody and cytokine therapeutics to treat patients with cancer and autoimmune diseases in the United states and internationally. The company's product candidates include Obexelimab, an immune inhibitor that has completed Phase 2 clinical trial for the treatment of IgG4-related disease and systemic lupus erythematosus, as well as in Phase 1b/2a clinical trial to treat moderate-to-severe rheumatoid arthritis; Plamotamab, a tumor-targeted antibody, which is in Phase 1 clinical trial to treat non-Hodgkin lymphoma; XmAb717, XmAb841, and XmAb104, a bispecific antibody that is in Phase 1 clinical trial to treat patients with selected advanced solid tumors; and Vibecotamab, which is in Phase 1 clinical trial for the treatment of acute myeloid leukemia and other CD123-expressing hematologic malignancies. It is also developing Tidutamab that is in Phase 1 clinical trial to treat neuroendocrine tumors and gastrointestinal stromal tumors; XmAb564 to treat Autoimmune diseases; XmAb819 for the treatment of renal cell carcinoma; and XmAb306/RO7310729, which is in Phase 1 clinical trial to treat solid tumors. In addition, the company provides Monjuvi for the treatment of adult patients with relapsed or refractory diffuse large B-cell lymphoma; Ultomiris to treat adult patients with paroxysmal nocturnal hemoglobinuria (PNH) and atypical hemolytic uremic syndrome; and AIMab7195 to reduce blood serum levels of IgE, which mediates allergic responses and allergic disease. It has a collaboration and license agreement with Genentech, MorphoSys AG, Nestlé S.A., Novartis AG, INmune Bio, Inc., Janssen Biotech, Inc., Astellas Pharma, Inc., Amgen Inc., Atreca, Inc., Janssen Biotech, Inc.; and The University of Texas MD Anderson Cancer Center. Xencor, Inc. was incorporated in 1997 and is headquartered in Monrovia, California.
Latest MGNX
- Senior VP, GC, and Secretary Peters Jeffrey Stuart sold $129,086 worth of shares (31,105 units at $4.15) as part of a pre-agreed trading plan, closing all direct ownership in the company (SEC Form 4)
- Sr VP, Research & CSO Bonvini Ezio exercised 40,000 shares at a strike of $2.60, increasing direct ownership by 27% to 185,799 units (SEC Form 4)
- SEC Form 10-Q filed by MacroGenics Inc.
- MacroGenics Inc. filed SEC Form 8-K: Results of Operations and Financial Condition, Financial Statements and Exhibits
- MacroGenics Reports Second Quarter 2026 Financial Results, Streamlined Operating Model and Strengthened Financial Position
- MacroGenics Announces Achievement of $10 Million Milestone Following Gilead’s Exercise of Option to License Preclinical Bispecific Program
- Amendment: SEC Form SCHEDULE 13G/A filed by MacroGenics Inc.
- MacroGenics Inc. filed SEC Form 8-K: Other Events, Financial Statements and Exhibits
- MacroGenics Provides Clinical Update on Ongoing Phase 1 Study for MGC026
- MacroGenics Inc. filed SEC Form 8-K: Leadership Update
Latest XNCR
- SEC Form 10-Q filed by Xencor Inc.
- Xencor Inc. filed SEC Form 8-K: Results of Operations and Financial Condition, Financial Statements and Exhibits
- Xencor Reports Second Quarter 2026 Financial Results
- Xencor Inc. filed SEC Form 8-K: Entry into a Material Definitive Agreement, Results of Operations and Financial Condition, Regulation FD Disclosure, Financial Statements and Exhibits
- Xencor to Receive $105 Million From Alexion to Resolve Ultomiris® U.S. Royalty Matter
- Xencor Announces Proffered Paper Oral Presentation at ESMO 2026 for Phase 1 Clinical Study of XmAb819 in Advanced Clear Cell Renal Cell Carcinoma
- Director Feigal Ellen was granted 10,302 shares, increasing direct ownership by 83% to 22,642 units (SEC Form 4)
- Director Gorman Kevin Charles was granted 10,302 shares, increasing direct ownership by 91% to 21,680 units (SEC Form 4)
- Director Gustafson Kurt A was granted 10,302 shares, increasing direct ownership by 70% to 25,011 units (SEC Form 4)
- Director Klencke Barbara was granted 10,302 shares, increasing direct ownership by 52% to 29,974 units (SEC Form 4)