News Releases

• 05/06/20

  Ryvu Therapeutics signs a grant agreement for the development of targeted immuno-oncology therapy

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• 03/06/20

  NodThera, Ryvu spin-off company, secures £44.5million ($54.5million) Series B Financing

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• 02/06/20

  Ryvu Therapeutics has completed the construction of the R&D Center for Innovative Drugs

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• 01/06/20

  Ryvu Therapeutics at BIO Digital 2020

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• 21/05/20

  Ryvu Therapeutics to Present at Jefferies 2020 Virtual Healthcare Conference

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• 18/05/20

  Ryvu Therapeutics to Present Recent Data from Multiple Oncology Programs at AACR 2020 Virtual Annual Meeting II

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• 14/05/20

  Ryvu Therapeutics announces availability of abstracts regarding Phase 1/2 study of SEL120 and SEL24/MEN1703 accepted for presentation at 25th EHA Congress

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• 16/04/20

  Galapagos and Ryvu announce research collaboration

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• 09/04/20

  Ryvu Therapeutics Reports Annual 2019 Financial Results

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• 31/03/20

  Ryvu Therapeutics To Present At Solebury Trout Virtual Investor Conference

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• 28/03/20

  Ryvu Therapeutics receives Orphan Drug Designation from FDA for SEL120 to treat Acute Myeloid Leukemia

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• 18/03/20

  Successful Completion of Phase I Clinical Study of SEL24/MEN1703 in Acute Myeloid Leukemia

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• 17/03/20

  Ryvu Therapeutics at BIO-Europe Spring 2020

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• 05/03/20

  Ryvu Therapeutics to Present at the 32nd Annual ROTH Conference

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• 26/02/20

  Ryvu Therapeutics signs a grant agreement for the development of targeted oncology therapies based on the synthetic lethality concept

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• 20/01/20

  Ryvu Therapeutics scientists as co-authors of Merck poster presentation on HIF-2alpha inhibitors

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• 17/01/20

  Ryvu Therapeutics together with scientists from the Jagiellonian University publish a synthetic lethality research paper in Biomolecules

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• 06/11/19

  Ryvu Therapeutics Announces Presentations on CDK8 Inhibitor SEL120 at the 61st ASH Annual Meeting

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• 06/11/19

  Ryvu Therapeutics Reports Third Quarter 2019 Financial Results

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• 05/11/19

  Ryvu Therapeutics to Present at BIO-Europe 2019

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• 14/10/19

  Ryvu Therapeutics Appoints Chief Medical Officer Setareh Shamsili, M.D., Ph.D., to Executive Management Board

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• 03/10/19

  Ryvu Therapeutics Announces Two Abstracts Accepted for Presentation at the Society for Immunotherapy of Cancer 34th Annual Meeting (SITC 2019)

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• 01/10/19

  Ryvu Therapeutics and Selvita Announce registration of Corporate Split by the National Court Register of Poland

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• 19/09/19

  Ryvu Announces Shareholder Approval of Corporate Split and New Name of Ryvu Therapeutics for Oncology Development Company

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• 06/09/19

  Ryvu Announces First Patient Dosed in Phase 1b Study of CDK8 Inhibitor SEL120 in the Treatment of Acute Myeloid Leukemia or High Risk Myelodysplastic Syndrome

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• 03/09/19

  Polish Financial Supervision Authority Approves Selvita CRO Prospectus, Allowing Corporate Split into Two Separately Listed Companies to Proceed

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• 25/07/19

  Selvita Appoints Setareh Shamsili, M.D., Ph.D., as Chief Medical Officer

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• 24/07/19

  Selvita to Present at Upcoming Conferences in September

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• 16/05/19

  Selvita announces availability of abstracts regarding Phase 1/2 study of SEL24/MEN1703 accepted for presentation at 2019 ASCO Annual Meeting and 24th EHA Congress

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• 13/05/19

  Selvita to Present at the UBS 2019 Global Healthcare Conference in New York

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• 17/04/19

  Poster regarding Phase 1/2 study of SEL24/MEN1703 accepted for the ASCO 2019 Annual Meeting

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• 04/04/19

  Selvita to present at the 2019 HCW Global Life Sciences Conference in London

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• 28/03/19

  Selvita to Separate Oncology Therapeutics and Contract Research Business Units into Two Global Companies

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• 26/03/19

  Selvita Announces U.S. FDA Acceptance of Investigational New Drug Application to Commence Clinical Development of SEL120 in the Treatment of Acute Myeloid Leukemia or High-Risk Myelodysplastic Syndrome

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• 04/03/19

  Selvita to Present Data from Multiple Oncology Programs at AACR 2019 Annual Meeting

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• 02/01/19

  Selvita to Present at Biotech Showcase 2019 in San Francisco

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• 21/11/18

  Selvita Announces Presentations on CDK8 Inhibitor SEL120 at the 60th American Society of Hematology Annual Meeting

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• 08/11/18

  Selvita to Present New Data from SEL120 Program at EORTC-NCI-AACR Symposium on Molecular Targets and Cancer Therapeutics

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• 31/10/18

  Selvita to present new data from its oncology programs at the upcoming SITC 2018

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• 03/10/18

  Selvita presents new data from SEL120 program during Leukemia and Lymphoma – Europe and the USA Linking Knowledge and Practice

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• 03/09/18

  Selvita presents at the 25th Annual BioCentury NewsMakers in the Biotech Industry

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• 27/08/18

  Selvita to present new data from its oncology programs at the 6th Annual Immuno-Oncology Summit

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• 26/04/18

  Institute of Hematology and Transfusion Medicine and Selvita publish joint research results on SEL24 potential in Chronic Lymphocytic Leukemia

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• 16/04/18

  Selvita publishes research results on SEL24 in Oncotarget

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• 06/04/18

  Selvita to present new data from its oncology programs at the upcoming AACR Annual Meeting 2018

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• 16/02/18

  Selvita Announces Successful Completion of $41 M Book Building

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• 16/12/17

  FDA lifts Clinical Hold on Selvita’s Phase I/II Clinical Trial with SEL24 in AML

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• 17/10/17

  Selvita researchers and academic collaborators demonstrate the potential of MNK1/2 kinase inhibitors in the treatment of c-Kit positive melanomas

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• 07/10/17

  Selvita Announces Full Clinical Hold on Phase I/II Clinical Trial of SEL24 in Acute Myeloid Leukemia

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• 03/10/17

  Selvita and Menarini present together at the European Business Development Conference

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• 08/08/17

  Selvita and The Leukemia & Lymphoma Society Announce Partnership to Advance SEL120 into Phase I for AML Patients

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• 13/07/17

  Institute of Hematology and Transfusion Medicine and Selvita publish joint research results in SEL24 project

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• 06/06/17

  Selvita presents at 18th Drug Discovery Summit in Berlin

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• 07/04/17

  Selvita researchers publish new paper on CDK8 inhibitor SEL120 in Oncotarget

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• 28/03/17

  Selvita and Menarini Group Announce Global License Agreement for Clinical Stage Oncology Drug PIM/FLT3 Inhibitor SEL24

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• 17/03/17

  Selvita Announces First Patient Dosed in Phase I/II Clinical Trial of SEL24 in Acute Myeloid Leukemia

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• 13/03/17

  Selvita to present new data from its oncology programs at the upcoming AACR Annual Meeting 2017

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• 13/02/17

  Selvita researchers publish MNK inhibitors review in Current Medicinal Chemistry

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• 16/12/16

  Selvita to present at Biotech Showcase 2017 in San Francisco

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• 30/11/16

  Selvita presents posters at 2016 EORTC-NCI-AACR Symposium

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• 18/08/16

  FDA has accepted Selvita’s IND application for the SEL24 Phase I/II clinical trial in AML

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• 18/08/16

  FDA has accepted Selvita’s IND application for the SEL24 Phase I/II clinical trial in AML

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• 28/07/16

  Epidarex Capital Creates Nodthera Limite

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• 06/06/16

  Selvita epigenetic project is the first Polish drug target program selected by EU Lead Factory

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• 01/02/16

  Selvita will present at the 18th Annual BIO CEO & Investor Conference 2016

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• 10/12/15

  Selvita wins the European Rising Star Award

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• 25/11/15

  The most recent data from Selvita’s SEL24 to be presented at the 57th ASH Annual Meeting & Exposition

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• 02/11/15

  Merck and Selvita Announce Drug Discovery Collaboration

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• 24/09/15

  Selvita launches new company – bioinformatics and personalized medicine focused Ardigen

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• 22/09/15

  H3 Biomedicine and Selvita Extend Precision Cancer Medicines Collaboration

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• 07/05/15

  Selvita receives the Economic Award of the President of Poland

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• 31/03/15

  Selvita initiates IND-enabling Studies for its first-in-class PIM/FLT3 inhibitor

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• 07/11/14

  Felicitex Therapeutics and Selvita initiate strategic collaboration to target cancer quiescence

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• 26/08/14

  Selvita and H3 Biomedicine will present at the Drug Discovery USA Congress 2014

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• 08/08/14

  New data from Selvita’s SEL24 will be presented by Institute of Hematology and Transfusion Medicine (IHT) at the ASH Meeting on Lymphoma Biology 2014

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