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home / articles / CLLS - Cellectis to Present Preliminary Results of NATHALI_01 and Updated Results of the BALLI_01 Phases I Trials at the American Society of Hematology (ASH) 65th Annual Meeting | Benzinga


CLLS - Cellectis to Present Preliminary Results of NATHALI_01 and Updated Results of the BALLI_01 Phases I Trials at the American Society of Hematology (ASH) 65th Annual Meeting | Benzinga

  • NEW YORK, Nov. 02, 2023 (GLOBE NEWSWIRE) --  Cellectis (the "Company") (NASDAQ:CLLS), a clinical-stage biotechnology company using its pioneering gene-editing platform to develop life-saving cell and gene therapies, announced today that preliminary results of the Phase I NATHALI-01 clinical trial evaluating UCART20x22 in patients with relapsed or refractory non-Hodgkin lymphoma (r/r NHL) and updated results of the Phase I BALLI-01 clinical trial evaluating UCART22 in patients with relapsed or refractory CD22+ B-cell acute lymphoblastic leukemia, (r/r B-ALL) will be presented at the American Society of Hematology 65th Annual Meeting (ASH 2023), that will take place on December 9-12, 2023 in San Diego (CA) and online.

    These data will be presented in two poster sessions:

    Poster Presentation (P2110)

    Title: Preliminary Results of Nathali-01: A First-in-Human Phase I/IIa Study of UCART20x22, a Dual Allogeneic CAR-T Cell Product Targeting CD20 and CD22, in Relapsed or Refractory (R/R) Non-Hodgkin Lymphoma (NHL) 

    Session Name: 704. Cellular Immunotherapies: Early Phase and Investigational Therapies: Poster I 

    Presenter: Dr. Jeremy Abramson (Massachusetts General Hospital Cancer Center)

    Date/Time: Saturday, December 9, 2023 at 5:30 - 7:30 PM PT at San Diego Convention Center, Halls G-H

    The poster presentation highlights the following data:

    • as of July 1, 2023, 3 patients were enrolled and treated at dose level 1 (50 million cells) with product manufactured in-house by Cellectis. Cytokine release syndrome (CRS) Grade 1 or 2 occurred in all patients, and all CRS resolved with treatment. 
    • No immune effector cell associated neurotoxicity (ICANS) or graft versus host disease (GvHD) was observed. There were no UCART20x22 dose limiting toxicities (DLTs), and there was 1 DLT in connection with CLLS52 (alemtuzumab). 
    • All patients responded at Day 28, with 1 partial metabolic response and 2 complete metabolic responses in patients who had failed prior autologous CD19 CAR T-cell therapies.
    • UCART20x22 expansion correlated with increases in serum cytokine and inflammatory marker levels as well as with CRS.
    • These initial data support the continued clinical trial evaluating UCART20x22 in R/R NHL. 

    Poster Presentation ...

    Full story available on Benzinga.com

  • Stock Information

    Company Name: Cellectis S.A.
    Stock Symbol: CLLS
    Market: NASDAQ
    Website: cellectis.com

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