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WKN: A1JUH2 | ISIN: PLSELVT00013 | Ticker-Symbol: 9Y4
Frankfurt
31.03.25
09:33 Uhr
7,050 Euro
+1,480
+26,57 %
Branche
Biotechnologie
Aktienmarkt
OSTEUROPA
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RYVU THERAPEUTICS SA Chart 1 Jahr
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25.02.Polish biotech Ryvu waves goodbye to 30% of staff in focus on phase 3 blood cancer trials3
25.02.Ryvu Therapeutics announces strategic reorganization to extend the cash runway for the development of RVU120 and the preclinical pipeline151Cash runway is extended from Q1 to H2 2026 with approximately €46 million (PLN 192 million) in cash and other financial assets held by Ryvu as of February 23,...
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25.02.Ryvu Therapeutics currently not interested in raising capital from market1
25.02.Ryvu Therapeutics plans group layoffs, halts recruitment of patients for clinical trial2
12.12.24Ryvu Therapeutics provides an update on RVU120 Phase II program288KRAKOW, Poland, Dec. 12, 2024 /PRNewswire/ -- Ryvu Therapeutics (WSE: RVU), a clinical-stage drug discovery and development company focusing on novel therapies...
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05.12.24Ryvu Therapeutics Announces Dosing of the First Patient in the POTAMI-61 Phase II Study of RVU120 for the Treatment of Patients with Myelofibrosis (MF)133The primary goal of the study is to evaluate the safety and efficacy of RVU120 in patients with myelofibrosis (MF), both as a single agent and in combination with...
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RYVU THERAPEUTICS Aktie jetzt für 0€ handeln
07.11.24Ryvu Therapeutics Reports 2024 Q3 Financial Results and Provides Corporate Update193In Q1-Q3 2024, Ryvu recognized total operating revenues (including grants) of USD 18.6 million, compared to USD 11.9 million in Q1-Q3 2023. Ryvu reports an acceleration...
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29.10.24Ryvu and nCage Partner to Develop Next-Generation ADC Platform4
19.09.24Ryvu Therapeutics Announces Dosing of the First Patient in the REMARK Phase II Study of RVU120 for the Treatment of Anemia in Patients with Lower-Risk Myelodysplastic Syndromes (LR-MDS)195Ryvu Therapeutics has announced the dosing of the first patient in the REMARK Phase II study of RVU120. The primary goal of the REMARK study is to evaluate the safety and efficacy of RVU120 in patients...
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12.09.24Ryvu Therapeutics Reports 2024 Half-Year Financial Results and Provides Corporate Update239The total operating revenues in H1 2024 amounted to USD 12.1 million and increased by USD 4.2 million compared to H1 2023. As of September, 5 2024, Ryvu's cash position was USD 65.3 million. Together...
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14.06.24Ryvu Therapeutics presents clinical and preclinical data on RVU120 at the 2024 European Hematology Association Congress261RVU120 as a single agent showed clinical benefit in heavily pretreated patients with AML and HR-MDS in the Phase 1 RIVER-51 study (CLI120-001). The strongest evidence of benefit was observed in patients...
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15.05.24Ryvu Therapeutics First Quarter 2024 Financial Results and Corporate Update222Total operating revenues in Q1 2024 amounted to $6.4M, compared to $4.3M in Q1 2023. As of May 9, 2024, Ryvu's cash position was $59.0M, inclusive of the first tranche of €8M in venture debt from...
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10.04.24Ryvu Therapeutics Presents Preclinical Data on RVU120 and Synthetic Lethality Programs at the 2024 AACR Annual Meeting196Ryvu PRMT5 inhibitors show potential best-in-class profiles, including a strong antiproliferative effect on MTAP-deleted cell lines and a good safety window versus MTAP WT cells. Ryvu's WRN inhibitor...
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