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 PRESS RELEASE

Cellectis publie une nouvelle approche d'édition intronique pour le tr...

Cellectis publie une nouvelle approche d'édition intronique pour le traitement des maladies métaboliques congénitales par des cellules souches hématopoïétiques modifiées NEW YORK, 10 avr. 2024 (GLOBE NEWSWIRE) -- Cellectis (Euronext Growth: ALCLS - Nasdaq: CLLS), société de biotechnologie de stade clinique, qui utilise sa technologie pionnière d'édition de génome TALEN® pour développer de potentielles thérapies innovantes pour le traitement de maladies graves, a annoncé aujourd'hui la publication d'un article scientifique dans Molecular Therapy, démontrant que l'édition d'introns par TALE...

 PRESS RELEASE

Cellectis Publishes a Novel Intronic Gene Editing Approach For the Tre...

Cellectis Publishes a Novel Intronic Gene Editing Approach For the Treatment of Inborn Metabolic Diseases by Edited HSPCs NEW YORK, April 10, 2024 (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, announced today the publication of a new research paper in Molecular Therapy, demonstrating that TALEN-mediated intron editing of hematopoietic stem and progenitor cells (HSPCs) enables transgene expression restricted to the myeloi...

 PRESS RELEASE

Cellectis présentera deux posters sur un nouveau procédé d’édition par...

Cellectis présentera deux posters sur un nouveau procédé d’édition par TALEN® pour la correction et l’insertion de gènes dans les cellules souches et progénitrices hématopoïétiques (HSPCs) à l’ASGCT NEW YORK, 08 avr. 2024 (GLOBE NEWSWIRE) -- Cellectis (Euronext Growth: ALCLS - Nasdaq: CLLS), société de biotechnologie de stade clinique, qui utilise sa technologie pionnière d'édition de génome TALEN® pour développer de potentielles thérapies innovantes pour le traitement de maladies graves, a annoncé aujourd'hui que des données préliminaires explorant un nouveau procédé d'édition par TALEN®...

 PRESS RELEASE

Cellectis Announces Two Poster Presentations on Novel TALEN® Editing P...

Cellectis Announces Two Poster Presentations on Novel TALEN® Editing Process for Gene Correction and Gene Insertion in HSPCs at the ASGCT Annual Meeting NEW YORK, April 08, 2024 (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 preliminary data exploring novel TALEN® editing process in hematopoietic stem and progenitor cells (HSPCs) will be presented at the American Society of Gene and Cell Therapy (ASGC...

 PRESS RELEASE

CORRECTION : Information mensuelle relative au nombre total des droits...

CORRECTION : Information mensuelle relative au nombre total des droits de vote et d’actions composant le capital social (Article 223-16 du Règlement Général de l’Autorité des Marchés Financiers) PARIS, 05 avr. 2024 (GLOBE NEWSWIRE) -- Ce document corrige et remplace le communiqué de presse diffusé le 4 avril à 16:30 heure de l'Est. Place de cotation : Euronext Growth ISIN code: FR0010425595 DateNombre total d’actions composant le capital socialNombre total de droits de vote31/03/202471 953 53577 889 229 Pour de plus amples informations sur Cellectis, veuillez contacter :         Co...

 PRESS RELEASE

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) PARIS, April 04, 2024 (GLOBE NEWSWIRE) -- Listing market: Euronext Growth ISIN code: FR0010425595 DateTotal number of sharesin the capitalTotal number of voting rights03/31/202471,953,53577,889,229 For further information on Cellectis, please contact:      Media contact:        Pascalyne Wilson, Director, Communications, +33 (0)7 76 99 14 33, Patricia Sosa Navarro, Chief of Staff to the CEO, +33 (0)7 76 77 46 93, Investor Relations cont...

 PRESS RELEASE

Information mensuelle relative au nombre total des droits de vote et d...

Information mensuelle relative au nombre total des droits de vote et d’actions composant le capital social (Article 223-16 du Règlement Général de l’Autorité des Marchés Financiers) PARIS, 04 avr. 2024 (GLOBE NEWSWIRE) -- Place de cotation : Euronext Growth ISIN code: FR0010425595 DateNombre total d’actions composant le capital socialNombre total de droits de vote29/02/202471 953 53577 889 229 Pour de plus amples informations sur Cellectis, veuillez contacter :         Contact média :         Pascalyne Wilson, Director, Communications, +33 (0)7 76 99 14 33, Patricia Sosa Navarro...

 PRESS RELEASE

CRISPR Therapeutics to Present at the Annual Needham Virtual Healthcar...

CRISPR Therapeutics to Present at the Annual Needham Virtual Healthcare Conference ZUG, Switzerland and BOSTON, April 03, 2024 (GLOBE NEWSWIRE) -- CRISPR Therapeutics (Nasdaq: CRSP), a biopharmaceutical company focused on creating transformative gene-based medicines for serious diseases, today announced that members of its senior management team will present at the Annual Needham Virtual Healthcare Conference on Wednesday, April 10, 2024, at 11:45 a.m. ET. A live webcast of the fireside chat will be available on the "Events & Presentations" page in the Investors section of the Company's ...

Jacob Mekhael ... (+2)
  • Jacob Mekhael
  • Thomas Vranken

Autolus FIRST LOOK: European dossier acceptance for obe-cel

The EMA has accepted the marketing authorisation application for review of obe-cel for r/r B-ALL, following the earlier acceptance by the FDA in January 2024. Looking ahead, Autolus is set for an eventful year with the FDA decision on obe-cel (PDUFA 16 November), as well as multiple data readouts including initial data from the phase 1 SLE trial by YE24, which we think could position obe-cel to become a pipeline in a product. We reiterate our BUY rating and $11 TP.

 PRESS RELEASE

Autolus Therapeutics announces acceptance of Marketing Authorization A...

Autolus Therapeutics announces acceptance of Marketing Authorization Application (MAA) by the European Medicines Agency (EMA) for obecabtagene autoleucel (obe-cel) for Patients with Relapsed/refractory (r/r) Adult B-Cell Acute Lymphoblastic Leukemia (B-ALL) Submission includes results from pivotal Phase 2 FELIX study evaluating obe-cel in r/r B-ALLThe US marketing application is under review with a Prescription Drug User Fee Act (PDUFA) target action date of November 16, 2024 LONDON, April 02, 2024 (GLOBE NEWSWIRE) -- Autolus Therapeutics plc (Nasdaq: AUTL), a clinical-stage biopharmaceu...

 PRESS RELEASE

CRISPR Therapeutics to Present at the American Society of Gene & Cell ...

CRISPR Therapeutics to Present at the American Society of Gene & Cell Therapy (ASGCT) 2024 Annual Meeting ZUG, Switzerland and BOSTON, April 01, 2024 (GLOBE NEWSWIRE) -- CRISPR Therapeutics (Nasdaq: CRSP), a biopharmaceutical company focused on creating transformative gene-based medicines for serious diseases, today announced an oral presentation at the American Society of Gene & Cell Therapy (ASGCT) 2024 Annual Meeting, taking place May 7 – 11, 2024, in Baltimore, MD and virtually. Title: Development of an In Vivo Non-Viral Ocular Editing Platform and Application to Potential Treatments...

 PRESS RELEASE

Autolus Therapeutics Announces Changes to its Board of Directors

Autolus Therapeutics Announces Changes to its Board of Directors LONDON, April 01, 2024 (GLOBE NEWSWIRE) -- Autolus Therapeutics plc (Nasdaq: AUTL), a clinical-stage biopharmaceutical company developing next-generation programmed T cell therapies, today announces the appointment of Mike Bonney as Chairman of the Board, and Ravi Rao M.D., as Non-Executive Director. John H. Johnson advised the Board of his decision to step down from his role as Chairman of the Board and Non-Executive Director. These changes are effective as of today, April 1, 2024. “On behalf of the Board and Managemen...

Jacob Mekhael
  • Jacob Mekhael

Autolus FIRST LOOK: Uneventful FY23 results, obe-cel's PDUFA in r/r AL...

Autolus reported uneventful FY23 results, with approx. $ 240m in cash (plus $ 600m from the strategic collaboration with BioNTech and public equity raise in February 2024) – enough to fully support the commercialisation of obe-cel in r/r adult ALL, as well as support obe-cel's pipeline expansion towards pivotal data in autoimmunity. Looking ahead, Autolus is set for an eventful year with an FDA decision on obe-cel in r/r adult ALL (PDUFA 16 November), as well as multiple data readouts including ...

 PRESS RELEASE

Autolus Therapeutics Reports Full Year 2023 Financial Results and Busi...

Autolus Therapeutics Reports Full Year 2023 Financial Results and Business Updates Announced strategic collaboration and equity investment from BioNTech for aggregate proceeds of $250 million upfront, plus underwritten offering of ADSs for $350 million, for gross proceeds of $600 million received in February 2024Submitted a Biologics License Application (BLA) for obecabtagene autoleucel (obe-cel), a potentially transformational treatment for relapsed/refractory (r/r) adult B-cell Acute Lymphoblastic Leukemia (ALL), to the US Food & Drug Administration (FDA); Prescription Drug User Fee Act (...

 PRESS RELEASE

CRISPR Therapeutics Proposes New Appointment to the Board of Directors

CRISPR Therapeutics Proposes New Appointment to the Board of Directors ZUG, Switzerland and BOSTON, March 13, 2024 (GLOBE NEWSWIRE) -- CRISPR Therapeutics (Nasdaq: CRSP), a biopharmaceutical company focused on creating transformative gene-based medicines for serious diseases, today announced it proposes to elect Christian Rommel, Ph.D., to its Board of Directors at the Company’s annual general meeting to be held this year. “We are thrilled to welcome Christian to our Board of Directors,” said Samarth Kulkarni, Ph.D., Chief Executive Officer and Chairman of the Board of CRISPR Therapeutic...

Jacob Mekhael ... (+2)
  • Jacob Mekhael
  • Thomas Vranken

Autolus FIRST LOOK: MHRA certification for manufacturing site

Autolus' manufacturing site, the Nucleus, has obtained MIA and GMP certification from the MHRA, enabling production of global commercial and clinical product supply. We estimate the site to have a capacity of 2,000+ batches per year, sufficient to cover the company's launch in r/r ALL and beyond, while targeting a vein-to-delivery time of 16 days at launch. With ample capacity at launch, we do not expect Autolus to run into the manufacturing or supply issues experienced by other companies during...

 PRESS RELEASE

Autolus Therapeutics receives Medicines and Healthcare products Regula...

Autolus Therapeutics receives Medicines and Healthcare products Regulatory Agency (MHRA) certification for Nucleus commercial manufacturing site LONDON, March 12, 2024 (GLOBE NEWSWIRE) -- Autolus Therapeutics plc (Nasdaq: AUTL), a clinical-stage biopharmaceutical company developing next-generation programmed T cell therapies, today announces that following the most recent GMP inspection by the MHRA in February 2024, Autolus’ Nucleus manufacturing facility in Stevenage has obtained a Manufacturer’s Importation Authorisation (MIA) together with the accompanying GMP certificate. This authori...

 PRESS RELEASE

Autolus Therapeutics announces publication in Blood Cancer Journal

Autolus Therapeutics announces publication in Blood Cancer Journal LONDON, March 11, 2024 (GLOBE NEWSWIRE) -- Autolus Therapeutics plc (Nasdaq: AUTL), a clinical-stage biopharmaceutical company developing next-generation programmed T cell therapies, today announced a publication in Blood Cancer Journal entitled ‘Dual T-cell constant β chain (TRBC)1 and TRBC2 staining for the identification of T-cell neoplasms by flow cytometry.’ 1 Diagnosing leukemic T-cell malignancies poses challenges due to their resemblance to reactive T-cells. In the paper published by Pedro Horna of Mayo Clin...

 PRESS RELEASE

Information mensuelle relative au nombre total des droits de vote et d...

Information mensuelle relative au nombre total des droits de vote et d’actions composant le capital social PARIS, 04 mars 2024 (GLOBE NEWSWIRE) -- (Article 223-16 du Règlement Général de l’Autorité des Marchés Financiers) Place de cotation : Euronext Growth ISIN code: FR0010425595 DateNombre total d’actions composant le capital socialNombre total de droits de vote29/02/202471 751 20177 686 895 Pour de plus amples informations sur Cellectis, veuillez contacter :         Contact média :         Pascalyne Wilson, Director, Communications, +33 (0)7 76 99 14 33, Patricia Sosa ...

 PRESS RELEASE

Monthly information on share capital and company voting rights

Monthly information on share capital and company voting rights PARIS, March 04, 2024 (GLOBE NEWSWIRE) -- (Article 223-16 of General Regulation of the French financial markets authority) Listing market: Euronext Growth ISIN code: FR0010425595 DateTotal number of sharesin the capitalTotal number of voting rights02/29/202471,751,20177,686,895 For further information on Cellectis, please contact:      Media contact:        Pascalyne Wilson, Director, Communications, +33 (0)7 76 99 14 33, Patricia Sosa Navarro, Chief of Staff to the CEO, +33 (0)7 76 77 46 93,    Investor Relations co...

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