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Aandeel Celyad BRU:CYAD.BL, BE0974260896

  • 0,315 25 apr 2024 15:48
  • -0,005 (-1,56%) Dagrange 0,315 - 0,320
  • 776 Gem. (3M) 25,1K

Celyad 2021

3.900 Posts
Pagina: «« 1 ... 39 40 41 42 43 ... 195 »» | Laatste | Omlaag ↓
  1. forum rang 5 Hopende 12 mei 2021 14:41
    quote:

    BXL1070 schreef op 12 mei 2021 14:00:

    @hopende - kunnen we terug naar de essentie van het forum?

    We drijven wel erg af naar wat als, morgen, gisteren, COMPLEET zei dat, dit en ginder.

    Het zou fijn zijn terug wat inhoudelijke posts te lezen.
    en wat is de essentie ? personen die verkeerde info geven zeer inhoudelijke posts , soit nog 15 dagen en ik moet het niet meer volgen , alle succes gewenst aan jullie maar loop niet verder in de val
  2. rodney007 12 mei 2021 23:13
    13% erbij in de States,

    Met het lege boekje in Brussel en als de tijd er wat aandacht aan besteed zou het morgen wel eens groot feest kunnen worden.

    Celyad Oncology to Present Data from Phase 1 IMMUNICY-1 Trial of Non-Gene Edited Allogeneic CAR T Candidate CYAD-211 in Relapsed/Refractory Multiple Myeloma at the European Hematology Association Virtual Congress

    Celyad Oncology SA
    Wed, May 12, 2021, 10:01 PM·5 min read

    No Grade = 3 treatment-related adverse events nor evidence of Graft-versus-Host disease reported from the completed first dose-level (DL1) cohort of Phase 1 dose-escalation IMMUNICY-1 trial evaluating the shRNA-based anti-BCMA CAR T candidate, CYAD-211, for relapsed/refractory (r/r) multiple myeloma

    Initial clinical activity observed, with one confirmed partial response (PR) observed in this low dose (30x106 cells per infusion)

    MONT-SAINT-GUIBERT, Belgium, May 12, 2021 (GLOBE NEWSWIRE) -- Celyad Oncology SA (Euronext & Nasdaq: CYAD), a clinical-stage biotechnology company focused on the discovery and development of chimeric antigen receptor T-cell (CAR T) therapies for cancer, today announced that an abstract highlighting initial clinical data from the Phase 1 IMMUNICY-1 trial of CYAD-211 has been accepted for e-poster presentation at the upcoming European Hematology Association (EHA) Virtual Congress 2021

    Filippo Petti, Chief Executive Officer at Celyad Oncology, commented, “We are very pleased with the initial results from the low dose cohort of our first shRNA-based allogeneic candidate, CYAD-211, which has showed preliminary signs of clinical activity, including a confirmed partial response, with no evidence of Graft-versus-Host-Disease. We are encouraged by the observed clinical activity at such a low dose level and the overall steady progress of the trial to date. Our team is intently focused on further assessing whether shRNA-mediated knockdown can generate safe, functional and clinically relevant allogeneic CAR T-cells for the treatment of cancer while offering an alternative technology platform with key advantages over gene-editing. We are excited for the opportunity to present the latest safety, clinical activity and cell kinetic data for the program next month at EHA and look forward to future updates for the program throughout 2021 as we move towards our goal of establishing proof-of-concept for this dynamic platform.”

    CYAD-211 is an investigational, non-gene edited allogeneic CAR T candidate engineered to co-express a single hairpin RNA (shRNA) and a BCMA-targeting chimeric antigen receptor in development for the treatment of relapsed/refractory multiple myeloma (r/r MM). This non-gene editing technology, which does not permanently alter the genome integrity, is intended to decrease the potential safety risk associated with “off-target” genome modifications. This “All-in-One” Vector approach with one single transduction step avoids multiple genetic modifications and cost associated with additional GMP grade materials.

    EHA 2021 ePoster Presentation Details:

    The following abstract published today is now available on the EHA 2021 website. Following the presentation at the meeting, the posters will be available in the Scientific Publications section of Celyad Oncology’s website.

    Title: Objective response at low dose in the first-in-human IMMUNICY-1 trial evaluating non-gene edited allogeneic CYAD-211 anti-BCMA CAR T product in relapsed or refractory multiple myeloma
    Presenter: Dr. Sébastien Anguille, Antwerp University Hospital (UZA), Edegem, Belgium
    Topic: Gene therapy, cellular immunotherapy and vaccination - Clinical
    Date and Time: e-Poster available starting Friday, June 11, 2021 at 9:00 a.m. CEST
    Abstract Number: EP739

    About CYAD-211

    CYAD-211 is an investigational, shRNA-based allogeneic CAR T candidate for the treatment of r/r MM. CYAD-211 is engineered to co-express an anti-BCMA targeting chimeric antigen receptor and a single shRNA to knockdown the CD3? component of the T cell receptor complex.

    About IMMUNICY-1 Phase 1 trial

    The open-label, dose-escalation trial will evaluate the safety and clinical activity of CYAD-211 following cyclophosphamide and fludarabine preconditioning chemotherapy in patients with relapsed or refractory multiple myeloma. The trial will evaluate multiple dose levels of CYAD-211: 30x106, 100x106 and 300x106 cells per infusion. For more information, please visit www.clinicaltrials.gov, study identifier number NCT04613557.

    About Celyad Oncology SA

    Celyad Oncology SA is a clinical-stage biotechnology company focused on the discovery and development of CAR T therapies for cancer. The Company is developing a pipeline of allogeneic (off-the-shelf) and autologous (personalized) CAR T cell therapy candidates for the treatment of both hematological malignancies and solid tumors. Celyad Oncology was founded in 2007 and is based in Mont-Saint-Guibert, Belgium and New York, NY. The Company has received funding from the Walloon Region (Belgium) to support the advancement of its CAR T cell therapy programs. For more information, please visit www.celyad.com.

  3. Noob nr1 13 mei 2021 07:34
    (ABM FN) Celyad heeft positieve resultaten bereikt in een fase 1 studie naar haar middel tegen Multipel Myeloom. Dit bleek uit een persbericht van het biotechbedrijf woensdagavond na sluitingstijd van Wall Street.

    Celyad Oncology zal de data van de fase 1 IMMUNICY-1-studie van kandidaat-medicijn CYAD-211 bij repetitief revalair Multipel Myeloom presenteren tijdens het congres van de European Hematology Association, dat virtueel plaatsvindt vanwege de coronacrisis.

    Er werden geen belangrijke neveneffecten na de eerste dosis ontdekt. Wel werd initiële klinische activiteit waargenomen, met één gedeeltelijke respons bij lage dosis.

    Multipel Myeloom is een beenmergziekte die zich manifesteert in kwaadaardige woekeringen van plasmacellen.

    Door: ABM Financial News.
3.900 Posts
Pagina: «« 1 ... 39 40 41 42 43 ... 195 »» | Laatste |Omhoog ↑

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