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RenovoRx Announces Late-Breaking Oral Presentation at 2023 ESMO World Congress on Gastrointestinal Cancer - Vimarsana News

RenovoRx Announces Late-Breaking Oral Presentation at 2023 ESMO World Congress on Gastrointestinal Cancer

Company to Present Interim Analysis Secondary Endpoint Data Including Progression-free Survival from Phase III TIGeR-PaC Study, a Multi-center Open-label Study Evaluating RenovoGem™ to Treat... | May 25, 2023

TME Pharma N.V.: TME Pharma Provides Positive Clinical Update and 14-month Survival Data From GLORIA Expansion Arm Evaluating NOX-A12 in Combination With Radiotherapy and Bevacizumab in Glioblastoma - Vimarsana News

TME Pharma N.V.: TME Pharma Provides Positive Clinical Update and 14-month Survival Data From GLORIA Expansion Arm Evaluating NOX-A12 in Combination With Radiotherapy and Bevacizumab in Glioblastoma

83% of glioblastoma patients remain alive after 14 months on study, a percentage well above what is expected for the enrolled population of chemotherapy refractory patients Survival data will

Rain Oncology Inc. Announces Topline Results from Phase 3 MANTRA Trial of Milademetan for Treatment of Dedifferentiated Liposarcoma - Vimarsana News

Rain Oncology Inc. Announces Topline Results from Phase 3 MANTRA Trial of Milademetan for Treatment of Dedifferentiated Liposarcoma

Rain Oncology Inc. announced its topline pivotal Phase 3 MANTRA data. The trial, evaluating the efficacy, safety, and tolerability of milademetan in patients with dedifferentiated liposarcoma , did... | May 23, 2023

Legend Biotech Reports First Quarter 2023 Results and Recent Highlights - Vimarsana News

Legend Biotech Reports First Quarter 2023 Results and Recent Highlights

New and updated data from the CARTITUDE Clinical Development Program and LEGEND-2 study evaluating ciltacabtagene autoleucel will be presented at the 2023 American Society of Clinical Oncology ... | May 18, 2023

Ultragenyx Pharmaceutical Gets FDA Agreement to Expand GTX-102 Study - Vimarsana News

Ultragenyx Pharmaceutical Gets FDA Agreement to Expand GTX-102 Study

By Chris Wack Ultragenyx Pharmaceutical said Wednesday that the U.S. Food and Drug Administration has reviewed and agreed to a protocol amendment to a Phase 1/2 study evaluating the safety and... | May 17, 2023