IND Filing for PFL-002/VERT-002 for Patients with Solid Tumors Including NSCLC with MET Alterations
“We are looking forward to initiating the first-in-human trial of PFL-002/VERT-002 later this year. We are confident that this new drug holds significant promise, as a novel therapeutic option with a differentiated mechanism of action, for patients facing MET-altered solid tumors, including NSCLC” said Francesco Hofmann, Head of Research and Development for Medical Care at Pierre Fabre Laboratories.
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“For patients battling brain cancer and other CNS diseases, the ability to deliver more drug to the tumor site with far fewer systemic side effects, could fundamentally shift how we treat these conditions,” said Amir Heshmatpour, Executive Chairman of NeOnc Technologies. “Our clinical results to date underscore the therapeutic potential
Chris Ehrlich, CERo Therapeutics CEO added, “It is encouraging to conduct our trial at one of the most renowned cancer centers in the United States, which we believe is a validation of the scientific work performed to date with CER-1236. The assignment of clinical trial sites is an important milestone.
“First subject has been dosed for a phase 1b/2 clinical trial of HLX43 for Injection, the novel Programmed Death-Ligand 1 (PD-L1)-targeting antibody-drug conjugate (ADC) that developed by the company based on the collaboration with MediLink Therapeutics, in combination with the Henlius’ independently developed innovative anti-PD-1 monoclonal antibody (mAb) HANSIZHUANG (serplulimab
“This topline safety data release from our atezolizumab combination program is another significant milestone for Sonnet’s clinical development,” concluded Raghu Rao, Sonnet’s Interim Chief Executive Officer. “Safety of this extended PK version of IL-12 has been within expected levels and the comparison with dosing in healthy volunteers provided strong evidence
