108
Participants
Start Date
May 9, 2018
Primary Completion Date
May 31, 2021
Study Completion Date
May 31, 2021
CS1003
In the dose escalation part, the dose levels will be escalated following a modified 3+3 dose escalation scheme. In the dose expansion part, patients will be assigned to different groups based on their tumor type.
CS1003
CS1003 to be intravenously administered at the dose level determined during the dose escalation part
Regorafenib
Regorafenib to be orally administered at the protocol-specified dose level, once daily for the first 21 days of each 28-day cycle
Scientia Clinical Research Ltd, Randwick
Lead Sponsor
CStone Pharmaceuticals
INDUSTRY