EMA validates GSK’s application for myelofibrosis therapy
With a differentiated mechanism of action, momelotinib has inhibitory ability along three important signalling pathways, Janus kinase (JAK) 1, and JAK2 and activin A receptor type I (ACVR1).
The US Food and Drug Administration (FDA) has accepted Bristol Myers Squibb’s (BMS) supplemental new drug application (sNDA) for Camzyos (mavacamten) to treat adolescents aged 12 to under 18 years with symptomatic obstructive hypertrophic cardiomyopathy (oHCM).
The multi-target, multi-year partnership will combine the clinical and commercial knowledge of Rallybio in rare diseases with AbCellera’s antibody discovery engine for identifying optimal clinical candidates and providing
The second-generation PDT photosensitiser drug, REM-001 has undergone late-stage clinical development in previous clinical trials. The REM-001 therapy includes three parts, a laser light source, a light delivery
The application has been submitted for the combination of toripalimab, cisplatin and gemcitabine as the first-line treatment for locally recurrent or metastatic nasopharyngeal carcinoma (NPC) patients. The company