The antibody has shown promising results in preclinical studies, demonstrating 'superior' anti-tumour activity.
The U.S. Food and Drug Administration (FDA) has approved Fapon Biopharma’s Investigational New Drug (IND) application for ...
The update was delivered at the Keystone Symposia ‘Human Microbiome: Diversity, Selection and Adaptation’ held 18-21 February ...
Top-line Phase 2/3 data readout for COMPANION-002, evaluating tovecimig (CTX-009 - a DLL4 x VEGF-A bispecific antibody) in patients with biliary ...
Recombinant human TSH (rhTSH) was developed to provide TSH stimulation without the requirement for THST withdrawal and the resultant metabolic disturbance, and without the drawbacks associated with ...
This drug is being developed for PD patients with a glucocerebrosidase 1 (GBA1) gene (GBA-PD ... potentially disease-modifying mechanism of action, with the potential to delay clinical motor ...