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🚀 We are very pleased to share that our portfolio company Advesya has received approval from the European Medicines Agency (EMA) to initiate the phase 1/2 trial of its lead asset, CCTx-001, to address the medical needs of patients with acute myeloid leukemia (AML).   AML is a cancer of the bone marrow and the blood that progresses rapidly without treatment   The #RESOLVE AML 001 study will determine the recommended phase 2 dose of CCTx-001 and will assess safety, tolerability, and clinical activity in patients with relapsed/refractory AML.   #biopharma #innovation #hematology #oncology #clinicalstudy

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Andreas Wallnoefer

Senior Executive - Board Director and Advisor in Biotech and Pharma

1mo

Ksenija Pavletic , Jens H. , Erik Rutjens, Stéphane LAMEYNARDIE and Richard C. A. Sainson and team: Great job ! A testimony of scientific and operational excellence to develop a therapy with huge potential and hope for patients with AML ! Congratulations also to the founders Christophe FERRAND and Marina DESCHAMPS and our independent board colleague Stanley Frankel to this great team and company achievement

Gianpaolo Fogliatto

Sr. Business Development Director | Drug Discovery Europe | Charles River Laboratories

1mo

Congrats to all Advesya team for this important achievement

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Dr. Philipp Marchand

Partner, German, Swiss and European patent attorney

1mo

congratulations Jens H. ! looking forward to the results

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