Compare · ALLO vs CLLS
ALLO vs CLLS
Side-by-side comparison of Allogene Therapeutics Inc. (ALLO) and Cellectis S.A. (CLLS): market cap, price performance, sector, and recent activity on the wire.
Summary
- Both companies sit in the Health Care sector. ALLO focuses on Biotechnology: Biological Products (No Diagnostic Substances), while CLLS focuses on Biotechnology: Pharmaceutical Preparations.
- ALLO is the larger of the two at $617.8M, about 2.3x CLLS ($264.4M).
- ALLO has been more active in the news (11 items in the past 4 weeks vs 5 for CLLS).
- ALLO has more recent analyst coverage (25 ratings vs 9 for CLLS).
- Company
- Allogene Therapeutics Inc.
- Cellectis S.A.
- Price
- -
- -
- Market cap
- $617.8M
- $264.4M
- 1M return
- -
- -
- 1Y return
- -
- -
- Industry
- Biotechnology: Biological Products (No Diagnostic Substances)
- Biotechnology: Pharmaceutical Preparations
- Exchange
- NASDAQ
- NASDAQ
- IPO
- 2018
- 2015
- News (4w)
- 11
- 5
- Recent ratings
- 25
- 9
Allogene Therapeutics Inc.
Allogene Therapeutics, Inc., a clinical stage immuno-oncology company, develops and commercializes genetically engineered allogeneic T cell therapies for the treatment of cancer. It develops, manufactures, and commercializes UCART19, an allogeneic chimeric antigen receptor (CAR) T cell product candidate for the treatment of pediatric and adult patients with R/R CD19 positive B-cell ALL. The company also develops ALLO-501, an anti-CD19 allogeneic CAR T cell product candidate that is in Phase I clinical trial for the treatment of R/R non-Hodgkin lymphoma; and ALLO-501A, which is in Phase I/II clinical trial for the treatment R/R large B-cell lymphoma or transformed follicular lymphoma. In addition, it is developing ALLO-715, an allogeneic CAR T cell product candidate that is in a Phase I clinical trial for treating R/R multiple myeloma; ALLO-819, an allogeneic CAR T cell product candidates for the treatment of acute myeloid leukemia; ALLO-605, an allogeneic CAR T cell product candidate for the treatment of multiple myeloma; ALLO-647, an anti-CD52 monoclonal antibody; CD70 to treat renal cell cancer; and DLL3 for the treatment of small cell lung cancer and other aggressive neuroendocrine tumors. The company has license and collaboration agreements with Pfizer Inc.; Servier; Cellectis S.A.; and Notch Therapeutics Inc., as well as clinical trial collaboration agreement with SpringWorks Therapeutics, Inc. It also has a strategic collaboration agreement with The University of Texas MD Anderson Cancer Center for the preclinical and clinical investigation of allogeneic CAR T cell product candidates. The company was founded in 2017 and is headquartered in South San Francisco, California.
Cellectis S.A.
Cellectis S.A., a clinical stage biotechnological company, develops immuno-oncology products based on gene-edited T-cells that express chimeric antigen receptors to target and eradicate cancer cells. It operates through two segments, Therapeutics and Plants. The company is developing UCART19, an allogeneic T-cell product candidate for the treatment of CD19-expressing hematologic malignancies, such as acute lymphoblastic leukemia; ALLO-501 and ALLO-501A to treat relapsed/refractory diffuse large B-cell lymphoma and follicular lymphoma; ALLO-316 for the treatment of Renal Cell Carcinoma; UCART123 for the treatment of acute myeloid leukemia; and UCART22 to treat B-cell acute lymphoblastic leukemia. It is also developing UCARTCS1 and ALLO-715 for the treatment of multiple myeloma. In addition, the company produces high oleic soybean oil, other soybean products, and fiber wheat. It has strategic alliances with Allogene Therapeutics, Inc.; Les Laboratoires Servier; The University of Texas M.D. Anderson Cancer Center; and Iovance Biotherapeutics, as well as a strategic research and development collaboration with Cytovia Therapeutics, Inc. The company was founded in 1999 and is headquartered in Paris, France.
Latest ALLO
- Allogene Therapeutics Announces Journal of Clinical Oncology Publication of Phase 1 Results of ALLO-316 Highlighting First Durable Remissions Following Allogeneic CAR T for Treatment of Metastatic Solid Tumors
- SEC Form 4 filed by President and CEO Roberts Zachary
- Director Kazam Joshua A converted options into 47,700 shares, increasing direct ownership by 14% to 398,463 units (SEC Form 4)
- SEC Form 4 filed by Director Messemer Deborah M.
- SEC Form 4 filed by Director Mayo Stephen
- SEC Form 4 filed by Director Sato Vicki L
- SEC Form 4 filed by Director Witte Owen N.
- SEC Form 4 filed by Director Humer Franz B
- SEC Form 4 filed by Director Barrett Elizabeth A.
- Allogene Therapeutics Inc. filed SEC Form 8-K: Submission of Matters to a Vote of Security Holders, Other Events, Financial Statements and Exhibits
Latest CLLS
- Prolynx Names Simon Harnest as Chief Financial Officer and Amer Mirza, PhD, as Chief Scientific Officer as It Advances Multi-Program Obesity and Metabolic Disease Portfolio
- Amendment: SEC Form 6-K/A filed by Cellectis S.A.
- SEC Form 6-K filed by Cellectis S.A.
- SEC Form 6-K filed by Cellectis S.A.
- Cellectis Reports Results from Shareholders Meeting Held on June 25, 2026
- SEC Form 6-K filed by Cellectis S.A.
- Cellectis Presents Final Phase 1 Results of Lasme-cel and Preliminary Results on Eti-cel at EHA 2026 Congress
- SEC Form 6-K filed by Cellectis S.A.
- Cellectis Receives FDA RMAT Designation for lasme-cel, the First Allogeneic CAR-T Therapy in a Pivotal Trial for Patients with r/r B-ALL
- Barclays initiated coverage on Cellectis with a new price target