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Cellectis S.A. (CLLS)

NasdaqGM - NasdaqGM Real Time Price. Currency in USD
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19.40+0.10 (+0.52%)
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Neutralpattern detected
Previous Close19.30
Open19.63
Bid18.30 x 800
Ask20.59 x 900
Day's Range18.95 - 19.65
52 Week Range8.75 - 34.71
Volume249,602
Avg. Volume436,288
Market Cap819.291M
Beta (5Y Monthly)2.20
PE Ratio (TTM)N/A
EPS (TTM)-1.91
Earnings DateN/A
Forward Dividend & YieldN/A (N/A)
Ex-Dividend DateN/A
1y Target Est34.60
  • Monthly information on share capital and company voting rights
    GlobeNewswire

    Monthly information on share capital and company voting rights

    (Article 223-16 of General Regulation of the French financial markets authority) NEW YORK, April 12, 2021 (GLOBE NEWSWIRE) -- Listing market: Euronext Growth ISIN code: FR0010425595 DateTotal number of sharesin the capitalTotal number of voting rights03/31/202143,039,18049,104,029 About CellectisCellectis 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 www.cellectis.com. Follow Cellectis on social media: @cellectis, LinkedIn and YouTube. TALEN® is a registered trademark owned by Cellectis. For further information, please contact: Media contacts:Pascalyne Wilson, Communications Manager, +33776991433, media@cellectis.com IR contact:Simon Harnest, SVP, Corporate Strategy and Finance, 646-385-9008, simon.harnest@cellectis.com Attachment Voting_Rights_PR_March_EN_docx

  • Cellectis Completes Sale of $47 million through its ATM program
    GlobeNewswire

    Cellectis Completes Sale of $47 million through its ATM program

    NEW YORK, April 09, 2021 (GLOBE NEWSWIRE) -- Cellectis S.A. (NASDAQ: CLLS – EURONEXT GROWTH: ALCLS) (the “Company”), a clinical-stage biotechnological company employing its core proprietary technologies to develop best-in-class products based on gene-edited allogeneic CAR T-cells in the field of immuno-oncology, today announced that it has completed sales of approximately $47 million of American Depositary Shares (“ADS”) pursuant to the Company’s ATM program established on March 29, 2021 (the “ATM Sales”), through Jefferies LLC (“Jefferies”), acting as sales agent. Each ADS represents one ordinary share of the Company. In the ATM Sales, an aggregate of 2,415,630 new ADSs and the same number of underlying new ordinary shares have been issued to existing and new investors at an at-the-market price of $19.50 per new ADS. It is anticipated that the settlement and delivery of the new ordinary shares will take place on April 12, 2021. They will be admitted to trading on the market of Euronext Growth and the issued ADSs will trade on Nasdaq. A shelf registration statement on Form F-3 (including a prospectus) relating to Cellectis’ securities was filed with the SEC and became effective upon filing on June 2, 2020. Before purchasing ADSs in the offering, prospective investors should read the prospectus supplement and the accompanying prospectus, together with the documents incorporated by reference therein. Prospective investors may obtain these documents for free by visiting EDGAR on the SEC’s website at www.sec.gov. Alternatively, a copy of the prospectus supplement (and accompanying prospectus) relating to the offering may be obtained from Jefferies LLC, 520 Madison Avenue, New York, NY 10022 or by telephone at (877) 821-7388 or by email at Prospectus_Department@Jefferies.com. This press release shall not constitute an offer to sell or the solicitation of an offer to buy securities of the Company, nor shall there be any sale of such securities in any state or jurisdiction in which such offer, solicitation or sale would be unlawful. In particular, no public offering of ADSs has been made in Europe. Special Note Regarding Forward-Looking Statements This press release contains “forward-looking” statements within the meaning of the “safe harbor” provisions of the Private Securities Litigation Reform Act of 1995, including, but not limited to, statements regarding Cellectis’ securities offering and the settlement thereof. Words such as “anticipates,” “believes,” “expects,” “intends,” “projects,” “anticipates,” and “future” or similar expressions are intended to identify forward-looking statements. These forward-looking statements involve known and unknown risks, uncertainties and other factors that may cause Cellectis’ actual results, performance or achievements to be materially different from any future results, performance or achievements expressed or implied by the forward-looking statements. Further information on the risk factors that may affect company business and financial performance is included in Cellectis’ Annual Report on Form 20-F for the year ended December 31, 2020, and subsequent filings Cellectis makes with the SEC from time to time. Except as required by law, Cellectis assumes no obligation to update these forward-looking statements publicly, or to update the reasons actual results could differ materially from those anticipated in the forward-looking statements, even if new information becomes available in the future, except as required by law. For further information, please contact: Media contacts: Margaret Gandolfo, 646-628-0300,Communications ManagerMargaret.gandolfo@cellectis.com or Conor McGlodrick, 914-355-0927,Zeno GroupConor.Mcgoldrick@zenogroup.com IR contact: Simon Harnest, 646-385-9008Chief Investment Officersimon.harnest@cellectis.com Attachment FINAL ATM PROGRAM _EN

  • The Daily Biotech Pulse: Wave Life Sciences Pulls Plug On 2 Assets, Amarin's Vascepa Snags European Approval, Biocept Jumps On Earnings
    Benzinga

    The Daily Biotech Pulse: Wave Life Sciences Pulls Plug On 2 Assets, Amarin's Vascepa Snags European Approval, Biocept Jumps On Earnings

    Here's a roundup of top developments in the biotech space over the last 24 hours: Scaling The Peaks (Biotech Stocks Hitting 52-week Highs March 29) Edgewise Therapeutics, Inc. (NASDAQ: EWTX) (went public Friday) Gain Therapeutics, Inc. (NASDAQ: GANX) GW Pharmaceuticals plc (NASDAQ: GWPH) Universe Pharmaceuticals INC (NASDAQ: UPC) Down In The Dumps (Biotech Stocks Hitting 52-week Lows March 29) 4D Molecular Therapeutics, Inc. (NASDAQ: FDMT) AbCellera Biologics Inc. (NASDAQ: ABCL) Adagene Inc. (NASDAQ: ADAG) ADMA Biologics, Inc. (ADMA) Avidity Biosciences, Inc. (NASDAQ: RNA) Bellerophon Therapeutics, Inc. (NASDAQ: BLPH) Chiasma, Inc. (NASDAQ: CHMA) Decibel Therapeutics, Inc. (NASDAQ: DBTX) Epizyme, Inc. (NASDAQ: EPZM) Evaxion Biotech A/S (NASDAQ: EVAX) Freeline Therapeutics Holdings plc (NASDAQ: FRLN) Fusion Pharmaceuticals Inc. (NASDAQ: FUSN) Gracell Biotechnologies Inc. (NASDAQ: GRCL) IMARA Inc. (NASDAQ: IMRA) Kala Pharmaceuticals, Inc. (NASDAQ: KALA) Karyopharm Therapeutics Inc. (NASDAQ: KPTI) Landos Biopharma, Inc. (NASDAQ: LABP) Lava Therapeutics B.V. (NASDAQ: LVTX) (went public Friday) Lucira Health, Inc. (NASDAQ: LHDX) Longeveron Inc. (NASDAQ: LGVN) MorphoSys AG (NASDAQ: MOR) Olema Pharmaceuticals, Inc. (NASDAQ: OLMA) Oncorus, Inc. (NASDAQ: ONCR) Orphazyme A/S (NASDAQ: ORPH) (the company's arimoclomol flunked a Phase 2/3 study in patients with body myositis, a progressively debilitating muscle-wasting disease) PMV Pharmaceuticals, Inc. (NASDAQ: PMVP) Prometheus Biosciences, Inc. (NASDAQ: RXDX) Relay Therapeutics, Inc. (NASDAQ: RLAY) Repro Med Systems, Inc. (NASDAQ: KRMD) Sarepta Therapeutics, Inc. (NASDAQ: SRPT) Sensei Biotherapeutics, Inc. (NASDAQ: SNSE) Spruce Biosciences, Inc. (NASDAQ: SPRB) Talis Biomedical Corporation (NASDAQ: TLIS) SQZ Biotechnologies Company (NYSE: SQZ) Stocks In Focus Wave Life Sciences Stops Development Of 2 Huntington's Disease Drug Candidates After Failed Study Wave Life Sciences Ltd. (NASDAQ: WVE) announced data from the Phase 1b/2a trials evaluating investigational treatments WVE-120102 and WVE-120101, in Huntington's disease, showing both candidates did not produce statistically significant change in mutant huntingtin protein versus placebo after single or multiple doses. The company said it will stop the study of both candidates and instead focus on WVE-120103. WVE-120103, the company said, will be advanced into a Phase 1b/2a Huntington's disease study. The investigational asset uses new PN backbone chemistry modifications that demonstrate improved preclinical pharmacology, the company said. The stock was down 26.8% premarket at $5.19. Merck's Application For Keytruda-Chemo Combo Label Expansion In Early Stage Breast Cancer Hit With Rejection Merck & Co., Inc. (NYSE: MRK) said the Food and Drug Administration has issued a complete response letter regarding its supplemental biologics license application seeking approval for Keytruda for the treatment of patients with high-risk, early stage triple-negative breast cancer in combination with chemotherapy as a pre-operative treatment option, then continuing as a single agent as a post-operative treatment option after surgery. The company said it is reviewing the letter and will discuss next steps with the FDA. Tiziana Plans Phase 2 Study Of Lead Drug In COVID-19 Tiziana Life Sciences PLC (NASDAQ: TLSA) said it plans to advance development of Foralumab, its anti-CD3 human monoclonal antibody, into a Phase 2 COVID-19 study. The decision follows a recent clinical study in mild-to-moderate COVID-19 patients, which showed evidence that the nasally administered anti-CD3 monoclonal antibody reduced pulmonary and systemic inflammation and was well-tolerated. Since the anti-inflammatory effect of nasally administered Foralumab is through the modulation of the immune system and not by directly targeting COVID-19, it is likely to be effective against the newly identified strains of the coronavirus in the U.K., South Africa and Brazil, the company said. The stock was up 4.91% to $2.78 in premarket trading Tuesday. GlaxoSmithKline Agrees To Support Manufacturing of Novavax's COVID-19 Vaccine In UK GlaxoSmithKline plc (NYSE: GSK), Novavax, Inc. (NASDAQ: NVAX) and the U.K. Government Vaccines Taskforce announced an agreement in principle to support manufacturing of up to 60 million doses of Novavax's COVID-19 vaccine candidate NVX-CoV2373 for use in the U.K. GlaxoSmithKline will provide "fill and finish" manufacturing capacity at its Barnard Castle facility in the northeast of England beginning as early as May. The companies will negotiate a final agreement with additional terms and conditions. In premarket trading Tuesday, Novavax shares were edging down 1.01% to $172 and GlaxoSmithKline was retreating 1.09% to $36.29. Amarin's Vascepa Approved In Europe As Vazkepa Amarin Corporation plc (NASDAQ: AMRN) said the European Medicines Agency has approved the marketing authorization application for Vazkepa to reduce the risk of cardiovascular events in high-risk, statin-treated adult patients who have elevated triglycerides. Vazkepa, which goes by the brand name Vascepa in the U.S., was approved by the FDA in December 2019. The stock was advancing 3.75% to $6.36 premarket Tuesday. Related Link: The Week Ahead In Biotech (March 28-April 3): Acadia's Dementia Drug Update, Clinical Readouts, Few Earnings In Holiday-Shortened Week Roche's Spinal Muscular Dystrophy Drug Approved In Europe Roche Holding AG (OTC: RHHBY) said the European Commission has approved Evrysdi for the treatment of 5q spinal muscular atrophy in patients two months of age and older, with a clinical diagnosis of SMA Type 1, Type 2 or Type 3 or with one to four SMN2 copies. The condition causes muscle weakness and progressive loss of movement, and a significant unmet need remains, particularly in adults living with the condition. Roche is leading the clinical development of Evrysdi as part of a collaboration with the SMA Foundation and PTC Therapeutics, Inc. (NASDAQ: PTCT). Evrysdi was approved by the U.S. FDA in August 2020. Novartis Inks Deal To In-License Radioligand Therapy Assets Targeting Cancer, Gets European Nod For Multiple Sclerosis Drug Novartis AG (NYSE: NVS) said it has obtained exclusive worldwide rights to develop and commercialize therapeutic applications for a library of fibroblast activation protein-targeting agents including FAPI-46 and FAPI-74, through an assignment agreement with iTheranostics, Inc., an affiliate of SOFIE Biosciences, Inc. View more earnings on IBB The FAP assets were originally developed at the University of Heidelberg. The agreement also includes co-exclusive rights for Novartis to develop imaging applications for these assets. Separately, Novartis received European Commission marketing authorization for the use of Kesimpta in the treatment of relapsing forms of multiple sclerosis in adults with active disease defined by clinical or imaging features. Kesimpta, which is developed and marketed worldwide by Novartis under a license agreement with Genmab A/S (NASDAQ: GMAB), is the first B-cell therapy that can be self-administered once-monthly at home via the Sensoready autoinjector pen. Kezar Rises On Insider Buying Kezar Life Sciences, Inc. (NASDAQ: KZR) disclosed in a filing that Vassiliki Economides, its SVP of strategy and external affairs, bought 750 shares of the company at $10.19 per share. The stock rose 10.18% to $6.17 in after-hours trading. Earnings AbCellera's full-year 2021 revenue climbed 1,908% to $233.2 million, with the bulk of the increase due to royalty revenue of $198.3 million for its anti-COVID-19 antibody treatment bamlanivimab, which it has licensed to Eli Lilly and Company (NYSE: LLY). The company reversed to a profit of 45 cents per share from a loss of 1 cent per share. The stock jumped 14.13% premarket to $26.58. Vaxcyte, Inc. (NASDAQ: PCVX) reported a narrower loss of 41 cents per share for the fourth quarter of 2020. This was notably smaller than the loss of $3.69 per share reported for the year-ago quarter. Analysts had estimated a loss of 54 cents per share for the quarter. The stock was down 11.13% premarket at $20.20. Biocept, Inc.'s (NASDAQ: BIOC) fourth-quarter revenue increased from $1.8 million in 2019 to $18.5 million in 2020. The company reversed from a loss of $1.97 per share in the year-ago quarter to a profit of 14 cents per share. Analysts, on average, were estimating a loss of 27 cents per share for the quarter. The stock was up 16.7% premarket at $6.01. Celldex Therapeutics, Inc. (CLDX) reported fourth-quarter revenue of $3.8 million in 2020, up 322% year-over-year, with the increase primarily due to a $1.8-million milestone payment from the Rockefeller University. The loss per share narrowed from 64 cents to 55 cents. The company said it has sufficient cash runway to see it through 2023. The stock was down 8.4% premarket at $18.75. Offerings Cellectis S.A. (NASDAQ: CLLS) said it has filed a prospectus supplement with the SEC relating to an at-the-market program, pursuant to which it may offer and sell to eligible investors a total gross amount of up to $125 million of ADS, with each ADS representing one ordinary share of Cellectis. Applied Molecular Transport Inc. (NASDAQ: AMTI) said it has commenced an underwritten public offering of 2.5 million shares of its common stock. All of the shares in the proposed offering will be sold by the company. The stock fell 1.72% to $48 in after-hours trading. On The Radar Earnings BioNTech SE (NASDAQ: BNTX) (before the market open) PolarityTE, Inc. (NASDAQ: PTE) (before the market open) Pieris Pharmaceuticals, Inc. (NASDAQ: PIRS) (before the market open) Immatics N.V. (NASDAQ: IMTX) (before the market open) Forma Therapeutics Holdings, Inc. (NASDAQ: FMTX) (before the market open) Protalix BioTherapeutics, Inc. (NYSE: PLX) (before the market open) AngioDynamics, Inc. (NASDAQ: ANGO) (before the market close) Bellicum Pharmaceuticals, Inc. (NASDAQ: BLCM) (after the close) Daré Bioscience, Inc. (NASDAQ: DARE) (after the close) IGM Biosciences, Inc. (NASDAQ: IGMS) (after the close) Osmotica Pharmaceuticals plc (NASDAQ: OSMT) (after the close) EDAP TMS S.A. (NASDAQ: EDAP) (after the close) Dyadic International, Inc. (NASDAQ: DYAI) (after the close) INVO Bioscience, Inc. (NASDAQ: INVO) (after the close) CorMedix Inc. (NASDAQ: CRMD) (after the close) Spectrum Pharmaceuticals, Inc. (NASDAQ: SPPI) (after the close) Eledon Pharmaceuticals, Inc. (NASDAQ: ELDN) (after the close) Crinetics Pharmaceuticals, Inc. (NASDAQ: CRNX) (after the close) Related Link: Attention Biotech Investors: Mark Your Calendar For March PDUFA Dates See more from BenzingaClick here for options trades from BenzingaThe Week Ahead In Biotech (March 28-April 3): Acadia's Dementia Drug Update, Clinical Readouts, Few Earnings In Holiday-Shortened WeekHighlights From Day 2 Of Benzinga's Biotech Small Cap Conference© 2021 Benzinga.com. Benzinga does not provide investment advice. All rights reserved.