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     553  26 Kommentare Sangamo Therapeutics and Voyager Therapeutics Enter License Agreement for Epigenetic Regulation Treatment of Prion Disease

    Sangamo Therapeutics, Inc. (Nasdaq: SGMO), a genomic medicine company, and Voyager Therapeutics, Inc. (Nasdaq: VYGR), today announced the parties have entered into a definitive license agreement for a potential treatment of prion disease. Using its proprietary epigenetic regulation platform, Sangamo has developed zinc finger transcriptional regulators (ZF-TRs) which it believes can specifically and potently block expression of the prion protein, the pathogenic driver of prion disease. Sangamo’s ZF-TRs have been shown in animal models to significantly reduce expression of the prion protein in the brain, extend life span and limit formation of toxic prion aggregates. Under the agreement, Voyager has provided Sangamo with access to a capsid derived from Voyager’s proprietary TRACER platform. This capsid has been shown to effectively cross the blood-brain barrier when delivered intravenously in animal models.

    This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20230629259968/en/

    “Prion is a devastating, rapidly progressing and deadly disease, for which no treatment options currently exist,” said Sandy Macrae, Chief Executive Officer at Sangamo. “While evaluating delivery mechanisms for our zinc finger transcriptional regulators, we were pleased to identify Voyager’s capsid as being well suited to potentially achieve the specific central nervous system coverage required for this indication today. Our agreement with Voyager highlights the importance of collaboration to address difficult indications with significant unmet medical need. I’m excited to combine Sangamo’s cutting-edge epigenetic regulation capabilities with the delivery abilities of Voyager’s capsid to potentially create the first ever meaningful therapy for prion disease.”

    Under the terms of the agreement, Sangamo has received a non-exclusive license to combine a Voyager TRACER capsid with Sangamo’s ZF-TRs designed to treat prion disease. Sangamo is solely responsible for the research, development, manufacture and commercialization of any product candidates using the Voyager capsid. Voyager is eligible to earn certain license fees, royalties on potential commercial sales of any products using Voyager’s capsid, and, in the event the prion program is out licensed by Sangamo, a portion of all licensing revenues received with respect to this program. Sangamo expects to submit a potential IND for a product candidate treating prion disease in 2025.

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    Sangamo Therapeutics and Voyager Therapeutics Enter License Agreement for Epigenetic Regulation Treatment of Prion Disease Sangamo Therapeutics, Inc. (Nasdaq: SGMO), a genomic medicine company, and Voyager Therapeutics, Inc. (Nasdaq: VYGR), today announced the parties have entered into a definitive license agreement for a potential treatment of prion disease. Using its …

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    Avatar
    09.04.24 20:39:14
    Wasatch 25 Mio, Vanguard 12,6 Mio,Biogen 14,6 Mio, BlackRock 14 Mio, State Street 9,8 Mio.
    Sind 76 Mio Aktien, wenn ich richtig gerechnet habe. Fehlen also noch 14 Mio zur absoluten Mehrheit. Die sollten sich doch finden lassen!
    Mal sehen, ob Gegenanträge eintrudeln,
    Avatar
    09.04.24 15:37:38
    Zitat von tupper: Wasatch Advisors melden 25 Mio Aktien = 11,9%. Also haben sie doch einiges losgekriegt.


    Na das klingt nun doch nicht ganz so negativ für die nächste Zeit.
    Avatar
    09.04.24 10:18:55
    Wasatch Advisors melden 25 Mio Aktien = 11,9%. Also haben sie doch einiges losgekriegt.
    Avatar
    04.04.24 19:16:48
    HV am 04.06.
    Die wollen tatsächlich weitermachen!
    Anzahl der genehmigten Aktien soll auf 960 Mio erhöht werden, Incentives gibt es auch weiter und man will fröhlich weiterforschen und auf weitere Jahre hinaus Geld verbrennen.
    Als nächstes werden wohl ein Reverse-Split und dann wieder KEs kommen. So wird der jetzige innere Wert immer weiter verwässert und verringert. Erfolge bei neuronalen Krankheiten vielleicht in fünf Jahren. Die FDA wird sehr restriktiv sein, wenn es darum geht, Kapside Richtung Gehirn zu schicken. Aber vielleicht sollte Macrae das im Selbstversuch erledigen!
    Die einzige Hoffnung ist, dass die verblieben Instis sich auf eine andere Marschrichtung einigen.
    Avatar
    01.04.24 22:45:39
    Ich vermute, dass die KE gefloppt ist.

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