Ryvu Therapeutics S.A. Annual Report 2021

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Ryvu Therapeutics to receive from Menarini Group a development milestone based on an amended global License Agreement

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Ryvu Therapeutics receives approval to conduct Phase I/II study of RVU120 (SEL120) in patients with relapsed/refractory metastatic or advanced solid tumors in Spain

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Change order to the statement of work

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Galapagos NV exercises its exclusive option to license program with therapeutic potential in inflammatory diseases

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Ryvu Therapeutics Presents Clinical and Translational Data Updates at the 63rd American Society of Hematology (ASH) Annual Meeting and the 44th San Antonio Breast Cancer Symposium

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Notification from person discharging managerial responsibilities in the Company due to execution of the Stock Grant Program – Article 19 of MAR

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Ryvu Therapeutics S.A. Q3 2021 Financial Report

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Ryvu Therapeutics to highlight HPK1 and STING Programs at the upcoming SITC Conference

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Ryvu’s partner Menarini Group receives FDA Orphan Drug Designation for SEL24 (MEN1703) for the Treatment of Acute Myeloid Leukemia

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Clinical and Translational Data from RVU120 and SEL24(MEN1703) programs to be presented at the 63rd American Society of Hematology (ASH) Annual Meeting & Exposition and the 44th Annual San Antonio Breast Cancer Symposium (SABCS)

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Filing a lawsuit against Mota-Engil Central Europe S.A. in connection with construction of the Research and Development Center

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Ryvu Therapeutics H1 2021 Financial Report

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First Patient Dosed in Phase I/II Study of RVU120 (SEL120) in Patients with Relapsed/Refractory Metastatic or Advanced Solid Tumors

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Resignation of the Member of the Management Board

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Notification from Aviva Otwarty Fundusz Emerytalny Aviva Santander on exceeding the threshold of 5% of the total number of votes in the Company

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Notification from person discharging managerial responsibilities in the Company due to execution of the Stock Grant Program – Article 19 of MAR

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Notification from person discharging managerial responsibilities in the Company – Article 19 of MAR

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FDA lifts partial clinical hold on RVU120 (SEL120) Phase Ib study in acute myeloid leukemia and myelodysplastic syndrome

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Notifications from persons discharging managerial responsibilities in the Company – Article 19 of MAR

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