Phase 0 - Human data before phase 1

Phase 0 studies using microdosing can save time and lower costs when compared to phase I studies, as well reducing the exposure of humans and animals to new chemical entities. Of course, such studies cannot be a substitute for clinical trials at therapeutic doses.

As with other first-in-human studies Recipharm and CTC have partnered to take responsibility for the full program reducing the complexity.

Learn more about our capabilities by downloading our fact sheet below.
 
/sites/default/files/media/FactSheet_Phase-0-Human-data-before-phase-1.pdf
False
False