Early phase clinical development is essential to the overall drug R&D. The value of R&D won’t be maximized without higher success rates of clinical trials and lower costs. Theaking correct strategies and tactics are the guarantee of a successful drug development, which is you must know. This course, beginning with the macro strategies of the clinical design, taking the examples of oncology/non-oncology clinical trials, explains the phase I, statistics and the first-in-human (FIH), as well as the Proof of Concept (PoC) to transition to phase III, and gives tactical guidance on the operational level with more practices.