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Bristol Myers Squibb Receives European Commission Approval for LAG-3-Blocking Antibody Combination, Opdualag (nivolumab and relatlimab), for the Treatment of Unresectable or Metastatic Melanoma with Tumor Cell PD-L1 Expression < 1%

Opdualag is a first-in-class, fixed-dose dual immunotherapy combination treatment of the PD-1 inhibitor nivolumab and novel LAG-3-blocking antibody relatlimab In RELATIVITY-047, Opdualag more than
United States United Kingdom South Korea Samit Hirawat Bristol Myers Squibb European Commission

Camrelizumab in Combination with Rivoceranib (Apatinib) Significantly Prolonged Overall Survival and Progression-Free Survival vs. Sorafenib in Patients with Unresectable Hepatocellular Carcinoma in a Multinational Phase 3 Trial, a Joint Program with Elev | Antibodies

Camrelizumab in Combination with Rivoceranib (Apatinib) Significantly Prolonged Overall Survival and Progression-Free Survival vs. Sorafenib in Patients with Unresectable Hepatocellular Carcinoma in a Multinational Phase 3 Trial, a Joint Program with Elevar Therapeutics
France General South Korea Republic Of Korea Rivoceranib Apatinib Hengrui Pharma Elevar Therapeutics Inc

BeiGene Announces Data Presentations at ESMO 2022 Including Late-Breaking Oral Presentation for Tislelizumab in First-Line Unresectable Hepatocellular Cancer

10.09.2022 - BeiGene (NASDAQ: BGNE; HKEX: 06160; SSE: 688235), a global, science-driven biotechnology company focused on developing innovative and affordable medicines to improve treatment outcomes and access for patients worldwide, shared updates from its solid ... Seite 1
Mark Lanasa Chief Medical Officer Solid Tumors

Deciphera Pharmaceuticals, Inc. Presents Initial Phase 1 Single Agent Dose Escalation Data for First-in-Class ULK Inhibitor of Autophagy, DCC-3116, at the European Society for Medical Oncology (ESMO) Congress 2022

&ndash; DCC-3116 Was Well-tolerated with No Dose Limiting Toxicities or Treatment-Related Serious Adverse Events Observed &ndash; &ndash; Pharmacokinetic and Pharmacodynamic Data Across all Doses... | September 10, 2022
United States Hong Kong United Kingdom Matthewl Sherman Anthony Tolcher Deciphera Pharmaceuticals

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BeiGene Announces Data Presentations at ESMO 2022 Including Late-Breaking Oral Presentation for Tisl

Tislelizumab demonstrated non-inferiority for overall survival and favorable safety profile versus sorafenib in global Phase 3 trialAdditional poster presentations show breadth of tislelizumab global clinical development program as single-agent treatment and in combinationCAMBRIDGE, Mass. &amp; BASEL, Switzerland &amp; BEIJ...
France General United States United Kingdom South Korea Great Britain Kevin Mannix

Exelixis Announces Detailed Results from Phase 3 COSMIC-313 Pivotal Trial in Patients with Previousl

โ€“ Cabozantinib in combination with nivolumab and ipilimumab significantly reduced the risk of disease progression or death compared with the combination of nivolumab and ipilimumab โ€“โ€“ Median progression-free survival was not yet reached with the combination of cabozantinib, nivolumab and ipilimumab versus 11.3 month...
United States Toni Choueiri Susan Hubbard Vickil Goodman Lindsay Treadway Nancy Kohlberg

Exelixis Announces Detailed Results from Phase 3 COSMIC-313 Pivotal Trial in Patients with Previously Untreated Advanced Kidney Cancer at ESMO 2022

08.09.2022 - Exelixis, Inc. (Nasdaq: EXEL) today announced detailed results from COSMIC-313, an ongoing phase 3 pivotal trial evaluating the combination of cabozantinib (CABOMETYX), nivolumab and ipilimumab versus the combination of nivolumab and ipilimumab in ...
United States Vickil Goodman International Metastatic Daiichi Sankyo Company Genentech Inc Takeda Pharmaceutical Company

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