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Aandeel Merus NV OTC:MRUS.Q, NL0011606264

  • 48,740 7 mei 2024 22:00
  • +1,400 (+2,96%) Dagrange 47,410 - 48,760
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Merus NV forum geopend

1.038 Posts
Pagina: «« 1 ... 11 12 13 14 15 ... 52 »» | Laatste | Omlaag ↓
  1. KAKO 17 januari 2018 16:36
    Had gehoopt dat de geruchte rondom Juno ook een positief effect zouden hebben op de koers van Merus. Valt helaas nog tegen. Gelukkig geniet ik momenteel wel van de stijging van Juno :D

    Merus lijkt mij ook zeker een overnamekandidaat! Gisterenmiddag schreef ik nog op het forum van Juno dat ik een overname in 2018 niet uitsluit. Een paar uur later was het raak. Hopelijk hetzelfde voor Merus of juist zo lang mogelijk zelfstandig blijven. Pijplijn is iig indrukwekkend en de diverse samenwerkingen benadrukken ook de potentie van Merus. Hopelijk zijn we op korte termijn van het gezeur van Regeneron af.
  2. Pokerface 26 januari 2018 13:38
    PB:

    MERUS ANNOUNCES FIRST PATIENT DOSED IN A PHASE 2 CLINICAL TRIAL OF MCLA-128 IN TWO METASTATIC BREAST CANCER PATIENT POPULATIONS

    Combination trial to evaluate MCLA-128 in HER2-positive and hormone receptor-positive/HER2-low metastatic breast cancer patients
    UTRECHT, the Netherlands, Jan. 26, 2018 (GLOBE NEWSWIRE) -- Merus N.V. (Nasdaq:MRUS), a clinical-stage immuno-oncology company developing innovative bispecific antibody therapeutics (Biclonics®), today announced that the first patient has been dosed in a Phase 2, open-label, multi-center international clinical trial to evaluate MCLA-128 in two metastatic breast cancer (MBC) populations including HER2-positive MBC patients and hormone receptor positive/HER2-low MBC patients.

    MCLA-128 is a full-length IgG bispecific antibody with enhanced antibody-dependent cellular cytotoxicity (ADCC) targeting HER2 and HER3 receptors. MCLA-128 blocks the HER3 signaling pathway by employing a Dock & Block™ mechanism. MCLA-128 is designed to dock onto a specific region of the HER2 receptor to orientate MCLA-128’s HER3 binding arm to block HER2:HER3 heterodimerization. Oncogenic signaling through the HER3 pathway, even in the presence of high heregulin concentrations, may thus be effectively blocked.

    “Initiation of the Phase 2 clinical trial in patients with HER2-positive MBC populations and hormone receptor-positive/HER2-low MBC populations represents another key milestone for Merus,” said Ton Logtenberg, PhD., Chief Executive Officer. “With promising single agent activity observed in heavily-pretreated patients underscoring the potential of MCLA-128 in MBC, this study is designed to elucidate the activity of this important HER2/HER3-targeted candidate in combination with current standards of care in areas of unmet need. Concurrently, our study evaluating single agent activity for MCLA-128 in gastric, ovarian, endometrial and non-small cell lung (NSCL) cancers is ongoing and we anticipate defining a clinical plan for MCLA-128 in solid tumors beyond metastatic breast cancer starting the second quarter of 2018. In addition, we remain committed to the remainder of our pipeline candidates, including MCLA-117 in acute myeloid leukemia, which is currently in the clinic, MCLA-158 for the potential treatment of colorectal cancer, which we expect to enter the clinic in the first quarter of 2018, as well as MCLA-145, which we are developing with Incyte Corporation in solid tumors.”

    The MCLA-128 Phase 2 clinical trial is expected to enroll approximately 120 patients in total across the U.S. and Europe. The first cohort, HER2-positive MBC patients who are progressing on anti-HER2 therapies including TDM-1, will receive MCLA-128 in combination with trastuzumab and chemotherapy. In preclinical studies, synergistic activity of MCLA-128 and trastuzumab has been demonstrated to inhibit heregulin-driven tumor cell growth. The second cohort, MBC patients with confirmed hormone receptor positive status and HER2-low (immuno-histo-chemistry (IHC) HER2 1+ or 2+ and fluorescent in-situ hybridization (FISH) negative for HER2 amplification) who are progressing on hormone therapies and CDK4/6 inhibitors, will receive MCLA-128 in combination with endocrine therapy. In preclinical models, blocking of signaling through the HER3 pathway has been shown to synergize with endocrine therapy. The primary endpoint for both cohorts is the clinical benefit rate at 24 weeks. Additional details about the study can be found on ClinicalTrials.gov, using identifier NCT: NCT03321981.

    About MCLA-128
    MCLA-128 is designed to block HER3/heregulin-dependent tumor growth and survival as well as enhance immune-mediated cytotoxicity in tumors. MCLA-128 employs a Dock and Block™ mechanism in which the mode of HER2 receptor binding orientates the HER3 binding arm to effectively block oncogenic signaling through the HER2:HER3 heterodimer even under high heregulin concentrations. In addition, MCLA-128 is modified for enhanced ADCC in order to recruit and activate immune effector cells to directly kill tumor cells.


    Bron: phoenix.corporate-ir.net/phoenix.zhtm...
  3. forum rang 6 Tom3 26 januari 2018 21:48
    quote:

    fly like an eagle schreef op 12 januari 2018 18:59:

    Link van Merus presentatie bij JP Morgan en ziet er indrukwekkend uit. seekingalpha.com/article/4137218-meru...
    Met dank aan alle informatieverschaffers hier: ik heb vanavond nog 1000 stukjes naar binnen gehengeld tegen $ 18,83 per stuk. Door de gedaalde dollar is de prijs in euro`s wat gunstiger geworden. Over een week maar weer eens kijken. Zou hun leukemiemedicijn net zo krachtig zijn als dat van Argenx? Als daar een proof of concept geleverd wordt, zou dit ook een high-flyer kunnen worden.
1.038 Posts
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