ALCLS Cellectis SA

Monthly information on share capital and company voting rights

Monthly information on share capital and company voting rights

(Article 223-16 of General Regulation of the French financial markets authority)

NEW YORK, Jan. 06, 2021 (GLOBE NEWSWIRE) --

Listing market: Euronext Growth

ISIN code: FR0010425595

DateTotal number of shares

in the capital
Total number of voting rights
12/31/202042,780,18648,847,575

About Cellectis

Cellectis is developing the first of its kind allogeneic approach for CAR-T immunotherapies in oncology, pioneering the concept of off-the-shelf and ready-to-use gene-edited CAR T-cells to treat cancer patients. As a clinical-stage biopharmaceutical company with over 21 years of expertise in gene editing, Cellectis is developing life-changing product candidates utilizing TALEN®, its gene editing technology, and PulseAgile, its pioneering electroporation system to harness the power of the immune system in order to target and eradicate cancer cells.

As part of its commitment to a cure, Cellectis remains dedicated to its goal of providing life-saving UCART product candidates to address unmet needs for multiple cancers including acute myeloid leukemia (AML), B-cell acute lymphoblastic leukemia (B-ALL) and multiple myeloma (MM).

Cellectis headquarters are in Paris, France, with additional locations in New York and Raleigh, North Carolina. Cellectis is listed on the Nasdaq Global Market (ticker: CLLS) and on Euronext Growth (ticker: ALCLS). For more information, visit .

Follow Cellectis on social media: , and .

TALEN® is a registered trademark owned by Cellectis.

For further information, please contact:

Media contacts:

Jennifer Moore, SVP, Public Relations & NY Site Head 917-580-1088, 

IR contact:

Simon Harnest, SVP, Corporate Strategy and Finance, 646-385-9008,

PDF available at: 



EN
06/01/2021

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Reports on Cellectis SA

 PRESS RELEASE

Cellectis to Report Third Quarter Financial Results on November 7, 202...

Cellectis to Report Third Quarter Financial Results on November 7, 2025 NEW YORK, Oct. 31, 2025 (GLOBE NEWSWIRE) -- Cellectis (the “Company”) (Euronext Growth: ALCLS- NASDAQ: CLLS), a clinical-stage biotechnology company using its pioneering gene-editing platform to develop life-saving cell and gene therapies, today announced that it will report financial results for the third quarter 2025 ending September 30, 2025 on Friday, November 7, 2025 after the close of the US market. The press release will be available in the Investors section of Cellectis’ website: Cellectis will not host a c...

 PRESS RELEASE

Cellectis publiera ses résultats financiers du troisième trimestre le ...

Cellectis publiera ses résultats financiers du troisième trimestre le 7 novembre 2025 NEW YORK, 31 oct. 2025 (GLOBE NEWSWIRE) -- Cellectis (Euronext Growth: ALCLS - Nasdaq: CLLS), société de biotechnologie de stade clinique qui utilise sa plateforme pionnière d’édition du génome pour développer des thérapies cellulaires et géniques, publiera ses résultats financiers pour le troisième trimestre clos au 30 septembre 2025, le vendredi 7 novembre 2025 après la clôture du marché aux États-Unis. Le communiqué de presse sera disponible dans la section “Investisseurs” du site internet de Cellect...

 PRESS RELEASE

Cellectis’ R&D Day Highlights Lasme-cel’s Potential to Address Signifi...

Cellectis’ R&D Day Highlights Lasme-cel’s Potential to Address Significant Unmet Need for Patients with r/r B-ALL  ○ Efficacy: ORR of 68% with lasme-cel Process 2 (n=22), 83% at RP2D (n=12) and 100% in the target Phase 2 population (n=9) ○ Safety: in Phase 1 (n=40), lasme-cel was generally well-tolerated (including 1 case of grade 2 IEC-HS which resolved) ○ Durability: in patients who achieved MRD-negative CR/CRi, median OS was 14.8 months ○ In the target Phase 2 population, CR/CRi rate of 56% with ~80% of patients achieving MRD-negative status ○ In the target Phase 2 population, 100% p...

 PRESS RELEASE

Le R&D Day de Cellectis souligne le potentiel de lasmé-cel pour comble...

Le R&D Day de Cellectis souligne le potentiel de lasmé-cel pour combler un besoin médical majeur non satisfait chez les patients atteints de LAL-B en rechute ou réfractaire ○ Efficacité : taux de réponse global (ORR) de 68 % avec le Process 2 de lasmé-cel (P2) (n=22) ; 83 % à la dose recommandée de Phase 2 (RP2D, n=12) ; et 100 % dans la population cible de Phase 2 (n=9)1 ○ Sécurité : en Phase 1 (n=40), lasmé-cel a été globalement bien toléré - un cas de syndrome hémophagocytaire associé aux effecteurs immunitaires (IEC-HS) de grade 2, résolu ○ Durabilité : chez les patients en RC/RCi MRD...

 PRESS RELEASE

Cellectis Hosts R&D Day Today Showcasing Pipeline Progress and Long-Te...

Cellectis Hosts R&D Day Today Showcasing Pipeline Progress and Long-Term Value Drivers Event features full Phase 1 data and pivotal Phase 2 strategy for lasme-cel (UCART22) in r/r B-ALL NEW YORK, Oct. 16, 2025 (GLOBE NEWSWIRE) -- Cellectis (the “Company”) (Euronext Growth: ALCLS - NASDAQ: CLLS), a clinical-stage biotechnology company using its pioneering gene editing platform to develop life-saving cell and gene therapies, today hosts a R&D Day in New York City. The Company’s leadership team and key opinion leaders will present the full Phase 1 dataset and outline the pivotal Phase 2 tr...

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