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$3.30
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2026-09-04 10:31:24 EDT-$0.02
Healthcare
Biotechnology
NASDAQ
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Cellectis S.A. is a biotechnology firm in the clinical development stage, concentrating on the creation of immuno-oncology therapies. These therapies harness gene-edited ...

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$3.30
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Cellectis S.A. (NASDAQ: CLLS) is a French clinical-stage biotechnology company headquartered in Paris. The company’s core purpose is to use its gene-editing platform to engineer next-generation immune cell therapies—most notably off-the-shelf, allogeneic T-cell approaches—aimed at treating cancer and other hard-to-treat diseases. By engineering T cells to express chimeric antigen receptors ...Cellectis S.A. (NASDAQ: CLLS) is a French clinical-stage biotechnology company headquartered in Paris. The company’s core purpose is to use its gene-editing platform to engineer next-generation immune cell therapies—most notably off-the-shelf, allogeneic T-cell approaches—aimed at treating cancer and other hard-to-treat diseases. By engineering T cells to express chimeric antigen receptors (CARs) or other targeted constructs, Cellectis seeks therapies that can specifically bind to tumor-associated targets and eliminate malignant cells. From a business and product perspective, Cellectis operates primarily through development of a diversified immuno-oncology pipeline. Key programs described include UCART19 (targeting CD19-expressing blood cancers such as acute lymphoblastic leukemia), as well as ALLO-501 and ALLO-501A for diffuse large B-cell lymphoma and follicular lymphoma in relapsed/refractory settings, and ALLO-316 for renal cell carcinoma. Additional programs mentioned include UCART123 for acute myeloid leukemia and UCART22 for B-cell acute lymphoblastic leukemia, plus other oncology candidates such as UCARTCS1 and ALLO-715 for multiple myeloma. The company also maintains research and development collaborations and strategic partnerships, which are important for clinical development progression, technology integration, and broader commercialization pathways. Cost and BOM (bill of materials) considerations for cell therapies are fundamentally driven by complex manufacturing steps: sourcing or generating starting cells, gene-editing/relevant genetic modifications, formulation, and quality control (including release testing). While the provided dataset does not enumerate a BOM, Cellectis’ pipeline and clinical-stage profile typically imply significant R&D spend, scale-up of specialized cell manufacturing, and ongoing regulatory/quality infrastructure. Financial metrics provided (e.g., negative operating margins and free cash flow on a TTM basis) are consistent with a company in a development-intensive phase where expenditures for clinical trials and manufacturing scale-up can exceed revenues. Key people: André (Andre) Choulika is identified as founder and CEO (and also described historically as a founder/leadership figure). Cellectis was founded in 1999 and has built its strategy around proprietary genome editing and cell-therapy development. In terms of “wishes” and strategic direction (typical for companies of this stage), the near- to mid-term priorities generally include advancing clinical programs toward key readouts, expanding indication coverage with lead assets, strengthening manufacturing readiness for scalable supply, and translating clinical results into value through milestones, partnerships, and potential commercialization opportunities.
Founded
1999
Employees
229
CEO
Andre Choulika
Full Name
Cellectis S.A.
Sector
Healthcare
Industry
Biotechnology
ROE
-94.14%
Market Cap
$0.33B
Current Ratio
1.37
WACC
15.18%
ROIC
-67.38%

Contact Information

33 1 81 69 16 00
8, rue de la Croix Jarry, Paris, IF 75013

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