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Cellectis S.A. (CLLS)

NasdaqGM - NasdaqGM Delayed Price. Currency in USD
2.1100+0.1500 (+7.65%)
As of 11:09AM EDT. Market open.
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Chart Events
Neutralpattern detected
Previous Close1.9600
Open2.0700
Bid2.0700 x 3000
Ask2.1100 x 900
Day's Range1.9600 - 2.1100
52 Week Range1.7700 - 5.0400
Volume10,295
Avg. Volume145,715
Market Cap96.144M
Beta (5Y Monthly)2.00
PE Ratio (TTM)N/A
EPS (TTM)-1.9100
Earnings DateN/A
Forward Dividend & YieldN/A (N/A)
Ex-Dividend DateN/A
1y Target Est10.10
  • GlobeNewswire

    Monthly information on share capital and company voting rights

    (Article 223-16 of General Regulation of the French financial markets authority)NEW YORK, March 15, 2023 (GLOBE NEWSWIRE) -- Listing market: Euronext Growth ISIN code: FR0010425595 DateTotal number of sharesin the capitalTotal number of voting rights02/28/202355,583,76861,651,088 About CellectisCellectis is a clinical-stage biotechnology company using its pioneering gene-editing platform to develop life-saving cell and gene therapies. Cellectis utilizes an allogeneic approach for CAR-T immunothe

  • GlobeNewswire

    Cellectis Announces Poster Presentation on TALEN®-edited MUC1 CAR T-cells Targeting Triple Negative Breast Cancer at the American Association of Cancer Research (AACR) Annual Meeting

    NEW YORK, March 14, 2023 (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 preclinical data exploring purposeful armoring of CAR T-cells to enhance efficacy of MUC1 CAR T-cells in targeting triple-negative breast cancer, will be presented at the American Association of Cancer Research (AACR) Annual Meeting, to

  • GlobeNewswire

    Cellectis Provides Business Update and Reports Fourth Quarter and Full Year 2022 Financial Results

    Entered into a €40 million credit facility with the European Investment Bank and closed an approximatively $25 million follow-on equity offering to support Cellectis’ research, development and innovation activities Positive preliminary clinical data from Phase 1 BALLI-01 study (evaluating UCART22) for patients with r/r B-cell ALL presented in a Live Webcast; First patient dosed with UCART22 product candidate fully manufactured in-house Encouraging preliminary results from Phase 1 AMELI-01 study

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