FDA approves Biostar’s Phase II/III plans with utidelone injectable for NSCLC

FDA approves Biostar’s Phase II/III plans with utidelone injectable for NSCLC

Source: 
Clinical Trials Arena
snippet: 

Synthetic biology biopharma Biostar Pharma announced is ready to advance its utidelone injectable (UTD1) in patients with locally advanced or metastatic non-small cell lung cancer (NSCLC), following approval from the US Food and Drug Administration (FDA) for the study.