Cellectis
CLLSPhase 2Cellectis is a French-American biotech with 25 years of expertise in gene editing, focused on developing next-generation, 'off-the-shelf' CAR T-cell therapies to address significant unmet needs in oncology. The company's core platform combines its flagship TALEN® technology for ultra-precise genome editing with its PulseAgile electroporation system for efficient cellular engineering. With a robust pipeline of allogeneic CAR T candidates and strategic global partnerships with companies like Allogene, Servier, and AstraZeneca, Cellectis aims to transform cancer treatment by making cell therapies more accessible and scalable.
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AI Company Overview
Cellectis is a French-American biotech with 25 years of expertise in gene editing, focused on developing next-generation, 'off-the-shelf' CAR T-cell therapies to address significant unmet needs in oncology. The company's core platform combines its flagship TALEN® technology for ultra-precise genome editing with its PulseAgile electroporation system for efficient cellular engineering. With a robust pipeline of allogeneic CAR T candidates and strategic global partnerships with companies like Allogene, Servier, and AstraZeneca, Cellectis aims to transform cancer treatment by making cell therapies more accessible and scalable.
Technology Platform
Proprietary TALEN® gene-editing technology for precise DNA modification and PulseAgile® electroporation system for efficient cellular engineering, enabling the development of off-the-shelf allogeneic CAR T-cell therapies.
Pipeline Snapshot
66 drugs in pipeline
| Drug | Indication | Stage |
|---|---|---|
| UCART22 + CLLS52 | B-cell Acute Lymphoblastic Leukemia | Phase 1/2 |
| UCART20x22 + CLLS52 | B-cell Non-Hodgkin Lymphoma (B-NHL) | Phase 1/2 |
| UCART123 | Blastic Plasmacytoid Dendritic Cell Neoplasm (BPDCN) | Phase 1 |
| UCART123v1.2 | Relapsed/Refractory Acute Myeloid Leukemia | Phase 1 |
| UCART123 | Acute Myeloid Leukaemia | Phase 1 |
Funding History
3Total raised: $298M
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Competitive Landscape
Cellectis competes in the allogeneic CAR-T space against well-funded companies like Allogene Therapeutics, CRISPR Therapeutics, and Precision BioSciences. Its differentiation is based on the perceived precision and safety of its proprietary TALEN® gene-editing platform versus widely used CRISPR systems, and its integrated control of both editing and manufacturing technology.
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